H. Mizusawa

发表

Profound Cardiac Sympathetic Denervation Occurs in Parkinson Disease

Satoshi Orimo, Yoshinori Itoh, Toshiki Uchihara, 2005, Brain pathology.

Neural Substrates for Semantic Memory of Familiar Songs: Is There an Interface between Lyrics and Melodies?

K. Oda, Keiichi Kawasaki, H. Mizusawa, 2012, PloS one.

Visualization of Aβ42(43) and Aβ40 in senile plaques with end-specific Aβ monoclonals: Evidence that an initially deposited species is Aβ42(43)

T. Iwatsubo, Y. Ihara, N. Nukina, 1994, Neuron.

Cognitive status correlates with white matter alteration in Parkinson's disease

O. Abe, S. Aoki, S. Orimo, 2012, Human brain mapping.

Mutations in COQ2 in familial and sporadic multiple-system atrophy.

J. Trojanowski, S. Gilman, K. Shirahige, 2013, The New England journal of medicine.

The neurology of COVID-19 revisited: A proposal from the Environmental Neurology Specialty Group of the World Federation of Neurology to implement international neurological registries

M. T. Medina, M. Wasay, A. Buguet, 2020, Journal of the Neurological Sciences.

White Matter Alteration in Idiopathic Normal Pressure Hydrocephalus: Tract-Based Spatial Statistics Study

S. Aoki, K. Ito, M. Ishikawa, 2012, American Journal of Neuroradiology.

Different Patterns of Fornix Damage in Idiopathic Normal Pressure Hydrocephalus and Alzheimer Disease

T Yuasa, S. Aoki, T. Yuasa, 2012, American Journal of Neuroradiology.

Sequence‐dependent and independent inhibition specific for mutant ataxin‐3 by small interfering RNA

K. Taira, H. Mizusawa, T. Yokota, 2004, Annals of neurology.

123I-metaiodobenzylguanidine myocardial scintigraphy in Parkinson’s disease

S. Orimo, H. Mizusawa, H Mizusawa, 1999, Journal of neurology, neurosurgery, and psychiatry.

Efficient in vivo delivery of siRNA into brain capillary endothelial cells along with endogenous lipoprotein.

H. Mizusawa, T. Yokota, H. Kuwahara, 2011, Molecular therapy : the journal of the American Society of Gene Therapy.

Structural connectivity in spatial attention network: reconstruction from left hemispatial neglect

S. Aoki, H. Mizusawa, Kenji Ito, 2017, Brain Imaging and Behavior.

Classification of cerebellar atrophy using voxel-based morphometry and SPECT with an easy Z-score imaging system.

H. Mitoma, H. Mizusawa, H. Nishioka, 2010, Internal medicine.

Non-human primate model of amyotrophic lateral sclerosis with cytoplasmic mislocalization of TDP-43

J. Kumagai, T. Uchihara, F. Ono, 2012, Brain : a journal of neurology.

Vocal cord abductor paralysis in spinocerebellar ataxia type 1

H. Mizusawa, K. Tashiro, T. Tsunemi, 1999, Journal of neurology, neurosurgery, and psychiatry.

A −16C>T substitution in the 5′ UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano

Y. Fukushima, N. Matsumoto, Kunihiro Yoshida, 2006, Journal of Human Genetics.

Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31

H. Mizusawa, Y. Ando, K. Ishikawa, 2015, Journal of neurogenetics.

Depressive disorder may be associated with raphe nuclei lesions in patients with brainstem infarction.

H. Mizusawa, T. Hattori, S. Ishiai, 2017, Journal of affective disorders.

Morel's laminar sclerosis showing apraxia of speech: Distribution of cortical lesions in an autopsy case

H. Akiyama, H. Mizusawa, O. Yokota, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

Progressive Multifocal Leukoencephalopathy with Balanced CD4/CD8 T-Cell Infiltration and Good Response to Mefloquine Treatment.

T. Maehara, Y. Eishi, H. Mizusawa, 2016, Internal medicine.

Failure of mefloquine therapy in progressive multifocal leukoencephalopathy: Report of two Japanese patients without human immunodeficiency virus infection

T. Morio, M. Saijo, H. Mizusawa, 2013, Journal of the Neurological Sciences.

Sequential changes in the non-coding control region sequences of JC polyomaviruses from the cerebrospinal fluid of patients with progressive multifocal leukoencephalopathy

T. Kanda, J. Kira, M. Saijo, 2012, Archives of Virology.

Midkine Inhibits Caspase‐Dependent Apoptosis via the Activation of Mitogen‐Activated Protein Kinase and Phosphatidylinositol 3‐Kinase in Cultured Neurons

M. Michikawa, H. Mizusawa, T. Muramatsu, 1999, Journal of neurochemistry.

Dynamic imbalance in gait ataxia. Characteristics of plantar pressure measurements

Kohei Kubota, Hiroshi Mitoma, Sadao Morita, 2006, Journal of the Neurological Sciences.

Localization and trafficking of endogenous anterior pharynx-defective 1, a component of Alzheimer's disease related γ-secretase

P. Fraser, P. George-Hyslop, Haifeng Jin, 2010, Neuroscience Letters.

123 I-metaiodobenzylguanidine myocardial scintigraphy in Parkinson’s disease

S. Orimo, H. Mizusawa, T. Sugimoto, 1999 .

Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by “dual-fluorescence labeled PCR-restriction fragment length analysis”

T. Amino, H. Mizusawa, I. Kondo, 2008, Journal of Human Genetics.

Distal myopathy with rimmed vacuoles: Novel mutations in the GNE gene

I. Kanazawa, H. Mizusawa, J. Shimizu, 2002, Neurology.

A novel mutation in the GNE gene and a linkage disequilibrium in Japanese pedigrees

S. Tsuji, H. Mizusawa, H. Date, 2002, Annals of neurology.

Significance of Development and Reversion of Collaterals on MRI in Early Neurologic Improvement and Long-Term Functional Outcome after Intravenous Thrombolysis for Ischemic Stroke

M. Tomita, H. Mizusawa, S. Shintani, 2015, American Journal of Neuroradiology.

APP717 missense mutation affects the ratio of amyloid beta protein species (A beta 1-42/43 and a beta 1-40) in familial Alzheimer's disease brain.

I. Kanazawa, N. Nukina, N. Suzuki, 1994, The Journal of biological chemistry.

Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan

T. Asada, K. Kaneko, Y. Goto, 2003, Annals of neurology.

COVID-19 international neurological registries

M. T. Medina, M. Wasay, A. Buguet, 2020, Lancet Neurology.

Muscular abnormalities in experimental hypothyroidism of rats with special reference to the mounding phenomenon

I. Nonaka, H. Mizusawa, Y. Toyokura, 1984, Experimental Neurology.

Association of α1‐antichymotrypsin polymorphism with cerebral amyloid angiopathy

E. Otomo, Y. Itoh, H. Mizusawa, 1998 .

Sphingosine-1-Phosphate Receptor-1 Selective Agonist Enhances Collateral Growth and Protects against Subsequent Stroke

H. Mizusawa, T. Yokota, D. Yui, 2015, PloS one.

Initiative on Rare and Undiagnosed Disease in Japan

H. Mizusawa, Yuji Takahashi, 2021, JMA journal.

Subacute Supranuclear Palsy in anti-Hu Paraneoplastic Encephalitis

M. Kiyosawa, H. Emoto, H. Mizusawa, 2017, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

The Japanese space gravitational wave antenna—DECIGO

T. Ebisuzaki, S. Yoshida, K. Kokeyama, 2006 .

Lack of association of neprilysin polymorphism with Alzheimer's disease and Alzheimer's disease-type neuropathological changes

M. Yamada, E. Otomo, Y. Itoh, 2001, Journal of neurology, neurosurgery, and psychiatry.

Ataxic phenotype with altered CaV3.1 channel property in a mouse model for spinocerebellar ataxia 42

S. Tsuji, Yukihiro Nakamura, N. Matsumoto, 2019, Neurobiology of Disease.

Cell-type-specific alternative splicing in spinocerebellar ataxia type 6

H. Mizusawa, T. Tsunemi, K. Ishikawa, 2008, Neuroscience Letters.

Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt–Jakob disease: a reliability and agreement study

K. Nagata, T. Yuasa, Y. Shiga, 2012, BMJ Open.

ANovel Mutation in ELOVL 4 Leading to Spinocerebellar Ataxia ( SCA ) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia A Broadened Spectrum of SCA 34

S. Tsuji, N. Matsumoto, S. Morishita, 2015 .

A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34.

S. Tsuji, N. Matsumoto, S. Morishita, 2015, JAMA neurology.

An experimental study for analyzing nerve conduction velocity.

H. Mizusawa, T. Akatsuka, M. Tamaki, 1986, Electroencephalography and clinical neurophysiology.

Highly diffusion-sensitized tensor imaging of unilateral cerebral arterial occlusive disease.

H. Mizusawa, A. Shiraishi, K. Minematsu, 2005, AJNR. American journal of neuroradiology.

Hydrocephalus in the Otx2+/−Mutant Mouse

H. Mizusawa, S. Shoji, Y. Makiyama, 1997, Experimental Neurology.

Can Anti-AQP4 Antibody Damage the Blood-Brain Barrier?

H. Mizusawa, M. Nishizawa, I. Kawachi, 2014, European Neurology.

Reversible central neurogenic hyperventilation in an awake patient with multiple sclerosis

H. Mizusawa, T. Tsunemi, M. Takahashi, 2007, Journal of Neurology.

Short interfering RNA and the central nervous system: development of nonviral delivery systems

H. Mizusawa, T. Yokota, K. Nishina, 2013, Expert opinion on drug delivery.

Two region‐dependent pathways of eosinophilic neuronal death after transient cerebral ischemia

T. Kuroiwa, Haiyan Xu, H. Mizusawa, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Selective loss of Purkinje cells in a patient with anti-glutamic acid decarboxylase antibody-associated cerebellar ataxia

H. Mitoma, J. Shibahara, H. Mizusawa, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Cerebral networks for spontaneous and synchronized singing and speaking

I. Tatsumi, K. Yagi, H. Mizusawa, 2006, Neuroreport.

Proteolytic cleavage and cellular toxicity of the human α1A calcium channel in spinocerebellar ataxia type 6

H. Mizusawa, Takeshi Matsuoka, K. Ishikawa, 2003, Neuroscience Letters.

Progressive accumulation of ubiquitin and disappearance of α-synuclein epitope in multiple system atrophy-associated glial cytoplasmic inclusions: triple fluorescence study combined with Gallyas-Braak method

T. Mizutani, T. Uchihara, A. Nakamura, 2005, Acta Neuropathologica.

Deletion of vitamin E enhances phenotype of Alzheimer disease model mouse.

K. Jishage, T. Uchihara, H. Mizusawa, 2006, Biochemical and biophysical research communications.

Depletion of Vitamin E Increases Amyloid β Accumulation by Decreasing Its Clearances from Brain and Blood in a Mouse Model of Alzheimer Disease*

K. Jishage, T. Terasaki, H. Mizusawa, 2009, The Journal of Biological Chemistry.

Glycosphingolipid composition of primary cultured human brain microvascular endothelial cells

T. Kanda, H. Mizusawa, T. Kasama, 2004, Journal of neuroscience research.

Biochemical Characterization of the Core Structure of α-Synuclein Filaments*

T. Iwatsubo, M. Hasegawa, H. Mizusawa, 2002, The Journal of Biological Chemistry.

Title Clinical features of genetic Creutzfeldt-Jakob disease with V 180 I mutationin the prion protein gene

M. Tomita, H. Mizusawa, S. Murayama, 2017 .

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene

M. Tomita, H. Mizusawa, S. Murayama, 2014, BMJ Open.

Involvement of the spinal posterior horn in Gerstmann–Sträussler–Scheinker disease (PrP P102L)

E. Otomo, Y. Itoh, H. Mizusawa, 1999, Neurology.

A nationwide survey of episodic ataxia in Japan

H. Mizusawa, Yuji Takahashi, M. Takahashi, 2021, Neurology and Clinical Neuroscience.

Analyses of copy number and mRNA expression level of the alpha-synuclein gene in multiple system atrophy.

T. Amino, H. Mizusawa, T. Tsunemi, 2008, Journal of medical and dental sciences.

Variants associated with Gaucher disease in multiple system atrophy

J. Trojanowski, S. Gilman, Y. Kuroiwa, 2015, Annals of clinical and translational neurology.

Relocation of p25α/tubulin polymerization promoting protein from the nucleus to the perinuclear cytoplasm in the oligodendroglia of sporadic and COQ2 mutant multiple system atrophy

S. Ichinose, A. Kakita, Y. Eishi, 2014, Acta neuropathologica communications.

Relocation of p25α/tubulin polymerization promoting protein from the nucleus to the perinuclear cytoplasm in the oligodendroglia of sporadic and COQ2 mutant multiple system atrophy

S. Ichinose, A. Kakita, Y. Eishi, 2014, Acta Neuropathologica Communications.

Ubiquitinated αB-crystallin in glial cytoplasmic inclusions from the brain of a patient with multiple system atrophy

H. Mizusawa, H. Mori, A. Tamaoka, 1995, Journal of the Neurological Sciences.

Argentophilic intracytoplasmic inclusions in multiple system atrophy

I. Kanazawa, A. Mochizuki, Kiyoharu Inoue, 1992, Journal of Neurology.

An Early Change of Neurofibrillary Tangle Formation

S. Yen, H. Mizusawa, A. Hirano, 1990 .

Gene dosage effect in spinocerebellar ataxia type 6 homozygotes: A clinical and neuropathological study

Y. Eishi, H. Mizusawa, T. Iida, 2017, Journal of the Neurological Sciences.

Cytoplasmic Location of α1A Voltage-Gated Calcium Channel C-Terminal Fragment (Cav2.1-CTF) Aggregate Is Sufficient to Cause Cell Death

R. Dolmetsch, Takeo Kato, Y. Eishi, 2013, PloS one.

Reduced brain‐derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF‐immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum

Takeo Kato, Y. Eishi, Hitoshi Takahashi, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.

[Molecular genetic approach to spinocerebellar ataxias].

T. Amino, H. Mizusawa, K. Ishikawa, 2009, Rinsho shinkeigaku = Clinical neurology.

Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells

T. Mizutani, T. Kawanami, H. Mizusawa, 2001, Neurology.

A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan

H. Mizusawa, S. Shoji, K. Ishikawa, 2001, Journal of Human Genetics.

A clinical, genetic, neuropathological study in a Japanese family with SCA 6 and a review of Japanese autopsy cases of autosomal dominant cortical cerebellar atrophy

H. Mizusawa, O. Tone, R. Okeda, 1998, Journal of the Neurological Sciences.

Clinical evaluation of plasma exchange and high dose intravenous immunoglobulin in a patient with Isaacs' syndrome.

E. Oguni, H. Mizusawa, K. Ishii, 1994, Journal of neurology, neurosurgery, and psychiatry.

Prevalence of Autoantibodies and the Efficacy of Immunotherapy for Autoimmune Cerebellar Ataxia.

H. Mitoma, T. Nagatani, H. Mizusawa, 2016, Internal medicine.

123I-MIBG myocardial scintigraphy for differentiating Parkinson's disease from other neurodegenerative parkinsonism: a systematic review and meta-analysis.

S. Orimo, H. Mizusawa, Masahiko Suzuki, 2012, Parkinsonism & related disorders.

Progressive supranuclear palsy presenting with pure akinesia.

I. Kanazawa, A. Mochizuki, H. Mizusawa, 1993, Advances in neurology.

Progressive Encephalomyelitis with Rigidity and Myoclonus Resolving after Thymectomy with Subsequent Anasarca: An Autopsy Case

E. Ito, Y. Eishi, M. Sekine, 2018, Internal medicine.

Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort.

H. Mizusawa, K. Ishikawa, T. Yokota, 2019, Parkinsonism & related disorders.

Idiopathic cerebellar ataxia (IDCA): Diagnostic criteria and clinical analyses of 63 Japanese patients

Kunihiro Yoshida, H. Mizusawa, Yuji Takahashi, 2018, Journal of the Neurological Sciences.

Biochemical characterization of the core structure of alpha-synuclein filaments.

T. Iwatsubo, M. Hasegawa, H. Mizusawa, 2002, The Journal of biological chemistry.

The risk of iatrogenic Creutzfeldt‐Jakob disease through medical and surgical procedures

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

A case of cortical tremor as a variant of cortical reflex myoclonus.

E. Oguni, H. Mizusawa, S. Shoji, 1995, European neurology.

Mounding phenomenon

H. Mizusawa, Y. Toyokura, H. Sugita, 1983, Neurology.

Lithium Therapy Improves Neurological Function and Hippocampal Dendritic Arborization in a Spinocerebellar Ataxia Type 1 Mouse Model

C. Shaw, H. Zoghbi, E. Emamian, 2007, PLoS Medicine.

Low-Titer Anti-GAD-Antibody-Positive Cerebellar Ataxia

H. Mitoma, H. Mizusawa, H. Niwa, 2013, The Cerebellum.

Association between butyrylcholinesterase K variant and the Alzheimer type neuropathological changes in apolipoprotein E ε4 carriers older than 75 years

M. Yamada, E. Otomo, Y. Itoh, 1999, Journal of neurology, neurosurgery, and psychiatry.

Spinocerebellar ataxia type 6 with motor neuron loss: A follow-up autopsy report

R. Hayashi, S. Ohara, H. Mizusawa, 2002, Journal of Neurology.

Gluten Ataxia in Japan

H. Mitoma, H. Mizusawa, M. Ihara, 2014, Cerebellum.

Is Anti-Gliadin Antibody Pathogenic in Gluten Ataxia? Analysis using Rat Cerebellar Slices and Patch-Clamp Recording

H. Mitoma, H. Mizusawa, K. Nanri, 2013 .

Serum level of soluble CX3CL1/fractalkine is elevated in patients with polymyositis and dermatomyositis, which is correlated with disease activity

N. Miyasaka, H. Mizusawa, T. Imai, 2012, Arthritis Research & Therapy.

Chimeric Antisense Oligonucleotide Conjugated to α-Tocopherol

H. Mizusawa, S. Ito, T. Yokota, 2015, Molecular therapy. Nucleic acids.

Chronic inflammatory demyelinating polyneuropathy: decreased claudin-5 and relocated ZO-1

T. Kanda, H. Mizusawa, Y. Numata, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Frontotemporal lobar degeneration with motor neuron disease showing severe and circumscribed atrophy of anterior temporal lobes

H. Akiyama, H. Mizusawa, T. Arai, 2010, Journal of the Neurological Sciences.

Clinicopathological characteristics of FTLD-TDP showing corticospinal tract degeneration but lacking lower motor neuron loss

H. Akiyama, H. Mizusawa, M. Onaya, 2010, Journal of the Neurological Sciences.

Randomized phase 2 study of perampanel for sporadic amyotrophic lateral sclerosis

G. Sobue, T. Kanda, K. Abe, 2021, Journal of Neurology.

LETTERS TO THE EDITOR RITUXIMAB THERAPY FOR MORVAN SYNDROME ASSOCIATED WITH MYASTHENIA GRAVIS

H. Mizusawa, K. Ishikawa, T. Yokota, 2012 .

Two distinct prions in fatal familial insomnia and its sporadic form

H. Mizusawa, S. Mohri, S. Murayama, 2019, Brain communications.

Myocardial nerve fibers are preserved in MPTP-treated mice, despite cardiac sympathetic dysfunction

T. Uchihara, T. Amino, S. Orimo, 2008, Neuroscience Research.

Down-regulation of an ankyrin repeat-containing protein, V-1, during skeletal muscle differentiation and its re-expression in the regenerative process of muscular dystrophy

I. Nonaka, Takayoshi Kobayashi, Si-young Song, 2003, Neuromuscular Disorders.

Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects

H. Mizusawa, K. Ishikawa, T. Yokota, 2017, Journal of the Neurological Sciences.

Abnormal RNA structures (RNA foci) containing a penta‐nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Y. Eishi, H. Mizusawa, E. Sugawara, 2013, Neuropathology : official journal of the Japanese Society of Neuropathology.

Pathological features of FTLD-FUS in a Japanese population: Analyses of nine cases

H. Akiyama, M. Hasegawa, S. Terada, 2013, Journal of the Neurological Sciences.

Triad proteins and intracellular Ca2+ transients during development of human skeletal muscle cells in aneural and innervated cultures

Takayoshi Kobayashi, H. Mizusawa, N. Kameda, 2004, Journal of Muscle Research & Cell Motility.

Posterior Cerebral Artery Laterality on Magnetic Resonance Angiography Predicts Long-Term Functional Outcome in Middle Cerebral Artery Occlusion

M. Tomita, H. Mizusawa, H. Fujigasaki, 2013, Stroke.

Association of alpha1-antichymotrypsin polymorphism with cerebral amyloid angiopathy.

E. Otomo, Y. Itoh, H. Mizusawa, 1998, Annals of neurology.

Immunocytochemical Studies of Substance P and Met-Enkephalin in the Globus Pallidus of Progressive Supranuclear Palsy

H. Mizusawa, S. Goto, A. Hirano, 1990 .

Cerebrospinal fluid endothelin-1 in Alzheimer's disease and senile dementia of Alzheimer type

I. Kanazawa, H. Mizusawa, H. Matsumoto, 1992, Neuropeptides.

Glycosphingolipid antibodies and blood–nerve barrier in autoimmune demyelinative neuropathy

H. Mizusawa, M. Yamawaki, T. Kanda, 2000, Neurology.

An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5 (cid:1) Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains Autosomal dominant cerebellar ataxia

T. Mizutani, J. Kumagai, T. Amino, 2005 .

Upper limits from the LIGO and TAMA detectors on the rate of gravitational-wave bursts

M. M. Casey, Robert Eliot Spero, Zheng Hong Zhu, 2005 .

Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage

R. Kaji, H. Mizusawa, M. Nishizawa, 2012, Journal of Human Genetics.

Very early onset Alzheimer's disease with spastic paraparesis associated with a novel presenilin 1 mutation (Phe237Ile)

M. Yamada, E. Otomo, Y. Itoh, 2001, Journal of neurology, neurosurgery, and psychiatry.

Blood–brain barrier destruction determines Fisher/Bickerstaff clinical phenotypes: an in vitro study

T. Kanda, S. Kusunoki, H. Mizusawa, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Hereditary neuropathy with liability to pressure palsy combined with suspected schwannomas of the peroneal and radial nerves

H. Mizusawa, T. Yokota, N. Sanjo, 2012, Journal of Neurology.

Long-term Effects of Intravenous Cyclophosphamide in Combination with Mesna Provided Intravenously and via Bladder Perfusion in a Patient with Severe Multifocal Motor Neuropathy

T. Kanda, H. Mizusawa, T. Yokota, 2017, Internal medicine.

Pure cerebellar ataxia phenotype in Machado-Joseph disease

S. Tsuji, H. Mizusawa, S. Shoji, 1996, Neurology.

Alternative BSE risk assessment methodology for beef and beef offal imported into Japan.

T. Tsutsui, T. Onodera, N. Ishiguro, 2012, The Journal of veterinary medical science.

Update: Dura Mater Graft–Associated Creutzfeldt-Jakob Disease — Japan, 1975–2017

L. Schonberger, H. Mizusawa, Yosikazu Nakamura, 2018, MMWR. Morbidity and mortality weekly report.

Descriptive Epidemiology of Prion Disease in Japan: 1999–2012

H. Mizusawa, M. Yamada, T. Kitamoto, 2015 .

Motor nerve conduction study in cauda equina with high‐voltage electrical stimulation in multifocal motor neuropathy and amyotrophic lateral sclerosis

H. Mizusawa, Y. Numasawa, T. Yokota, 2011, Muscle & nerve.

Occurrence of basophilic inclusions and FUS-immunoreactive neuronal and glial inclusions in a case of familial amyotrophic lateral sclerosis

H. Akiyama, M. Hasegawa, H. Mizusawa, 2010, Journal of the Neurological Sciences.

A possible novel isoform of peripheral myelin P0 protein: a target antigen recognized by an autoantibody in a patient with malignant lymphoma and peripheral neuropathy

R. Takahashi, H. Mizusawa, M. Yamada, 2001, Journal of the Neurological Sciences.

Enteral siRNA delivery technique for therapeutic gene silencing in the liver via the lymphatic route

N. Nishiyama, K. Kataoka, H. Mizusawa, 2015, Scientific Reports.

Effects of pericytes and various cytokines on integrity of endothelial monolayer originated from blood-nerve barrier: an in vitro study.

T. Kanda, H. Mizusawa, T. Iwasaki, 1999, Journal of medical and dental sciences.

Glial expression of presenilin epitopes in human brain with cerebral infarction and in astrocytoma

P. Fraser, T. Uchihara, A. Nakamura, 1999, Acta Neuropathologica.

Bax-inhibiting peptide protects cells from polyglutamine toxicity caused by Ku70 acetylation

D. Sinclair, Ignacio Aguaded, H. Cohen, 2007, Cell Death and Differentiation.

Involvement of hippocampus in Creutzfeldt-Jakob disease

H. Mizusawa, A. Hirano, J. Llena, 1987, Journal of the Neurological Sciences.

Self-secretion of fibroblast growth factor-9 supports basal forebrain cholinergic neurons in an autocrine/paracrine manner

T. Kanda, H. Mizusawa, T. Kurokawa, 2000, Brain Research.

Pseudopolyneuritic form of ALS revisited: Clinical and pathological heterogeneity

H. Akiyama, H. Mizusawa, O. Yokota, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Proliferating Immature Schwann Cells Contribute to Nerve Regeneration After Ischemic Peripheral Nerve Injury

H. Mizusawa, T. Yokota, H. Tomimitsu, 2012, Journal of neuropathology and experimental neurology.

Joint LIGO and TAMA300 search for gravitational waves from inspiralling neutron star binaries

M. M. Casey, Robert Eliot Spero, Zheng Hong Zhu, 2006 .

Amyloid β protein 1–42/43 (Aβ 1–42/43) in cerebellar diffuse plaques: enzyme-linked immunosorbent assay and immunocytochemical study

A. Odaka, H. Mizusawa, H. Mori, 1995, Brain Research.

Hyaline and Skein‐like Inclusions in Amyotrophic Lateral Sclerosis

H. Mizusawa, 1993 .

Screening of the mis-sense mutation producing the 717Val → Ile substitution in the amyloid precursor protein in Japanese familial and sporadic Alzheimer's disease

I. Kanazawa, H. Mizusawa, Y. Komatsuzaki, 1993, Journal of the Neurological Sciences.

Immune-mediated neuropathy with Epstein-Barr virus-positive T-cell lymphoproliferative disease.

H. Mizusawa, T. Hattori, O. Miura, 2015, Internal medicine.

No Association of Paraoxonase Genotype or Atherosclerosis With Cerebral Amyloid Angiopathy

E. Otomo, Y. Itoh, H. Mizusawa, 2002, Stroke.

Clinical features of the behavioural variant of frontotemporal dementia that are useful for predicting underlying pathological subtypes of frontotemporal lobar degeneration

H. Akiyama, H. Mizusawa, A. Shiraishi, 2018, Psychogeriatrics : the official journal of the Japanese Psychogeriatric Society.

An autopsy case of chronic active Epstein–Barr virus infection (CAEBV): Distribution of central nervous system (CNS) lesions

H. Akiyama, H. Mizusawa, O. Yokota, 2008, Journal of the Neurological Sciences.

Ophthalmic Surgery in Prion Diseases

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2007, Emerging infectious diseases.

Reversible acute axonal polyneuropathy associated with Wernicke-Korsakoff syndrome: impaired physiological nerve conduction due to thiamine deficiency?

T. Kanda, H. Hirota, H. Tanaka, 2003, Journal of neurology, neurosurgery, and psychiatry.

Spinal Epidural Abscess Caused by Bacteroides Fragilis Group after Dilation and Curettage for Incomplete Abortion

H. Mizusawa, A. Okawa, T. Yokota, 2012, Journal of global infectious diseases.

More than a 100-fold increase in immunoblot signals of laser-microdissected inclusion bodies with an excessive aggregation property by oligomeric actin interacting protein 2/D-lactate dehydrogenase protein 2.

K. Kaneko, H. Mizusawa, Y. Kozuka, 2005, Analytical biochemistry.

Progression of bilateral internal carotid artery dissection during antiplatelet therapy.

H. Mizusawa, T. Mizutani, Mafuyu Takahashi, 2013, Internal medicine.

Efficient regulation of viral replication by siRNA in a non-human primate surrogate model for hepatitis C.

Y. Iwasaki, K. Ishii, N. Ageyama, 2007, Biochemical and biophysical research communications.

Environmental challenges for the nervous system and the brain in Japan.

H. Mizusawa, J. Reis, 2019, Revue neurologique.

5. Prion Diseases: The Present Status and Prospect of Overcoming

H. Mizusawa, 2015 .

Tumor necrosis factor-related apoptosis-inducing ligand induces neuronal death in a murine model of HIV central nervous system infection

Mamoru Ito, N. Yamamoto, H. Mizusawa, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Current Evidence for the Association between Air Pollution and Parkinson's Disease

H. Mizusawa, Y. Saitoh, 2022, Annals of Indian Academy of Neurology.

FUS regulates RAN translation through modulating the G-quadruplex structure of GGGGCC repeat RNA in C9orf72-linked ALS/FTD

H. Taguchi, L. Petrucelli, K. Nakatani, 2022, bioRxiv.

Primary position upbeat nystagmus increased on downward gaze

H. Mizusawa, N. Ohkoshi, Y. Komatsu, 1998, Neurology.

Anhidrosis associated with hypothalamic lesions related to anti-aquaporin 4 autoantibody

H. Mizusawa, T. Yokota, T. Kanbayashi, 2011, Journal of Neurology.

Calbindin-D 28k immunoreactivity in the cerebellum of spinocerebellar degeneration

H. Mizusawa, S. Shoji, Y. Komatsuzaki, 1995, Journal of the Neurological Sciences.

18F-THK5351 positron emission tomography imaging for Gerstmann-Sträussler-Scheinker disease

E. Imabayashi, H. Matsuda, H. Mizusawa, 2022, Journal of the Neurological Sciences.

A comparison of long-term neurological symptoms after two different focal ischemic models in Mongolian gerbils.

T. Kuroiwa, H. Mizusawa, R. Okeda, 2003, Acta neurochirurgica. Supplement.

ORIGINAL RESEARCH Different Patterns of Fornix Damage in Idiopathic Normal Pressure Hydrocephalus and Alzheimer Disease

S. Aoki, T. Yuasa, H. Mizusawa, 2012 .

Elevated platelet microparticle levels after acute ischemic stroke with concurrent idiopathic thrombocytopenic purpura.

H. Mizusawa, S. Nomura, T. Yokota, 2014, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Quantifying prion disease penetrance using large population control cohorts

Patrick F. Sullivan, Karen L. Mohlke, M. Arfan Ikram, 2016, Science Translational Medicine.

Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene.

H. Mizusawa, M. Yamada, K. Satoh, 2018, Biochemical and biophysical research communications.

Creutzfeldt–Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP

H. Mizusawa, T. Kitamoto, S. Toru, 2004, Neurology.

An inherited prion disease with a PrP P105L mutation

Y. Wada, E. Otomo, Y. Itoh, 1999, Neurology.

Morphological Purkinje cell changes in spinocerebellar ataxia type 6

H. Mizusawa, N. Mitsuma, Mari Yoshida, 2000, Acta Neuropathologica.

Short communication Characteristic changes in T -value, apparent diffusion coefficient, and

T. Nagaoka, N. Miyasaka, T. Kuroiwa, 2001 .

Familial mitochondrial myopathy associated with peripheral neuropathy: Partial deficiencies of complex I and complex IV

I. Kanazawa, Hiroshi Suzuki, T. Ozawa, 1988, Journal of the Neurological Sciences.

Utility of F-18 FDG PET/CT in Screening for Paraneoplastic Neurological Syndromes

Kazunori Kubota, H. Mizusawa, H. Shibuya, 2012, Clinical nuclear medicine.

Acute autonomic and sensory neuropathy after interferon α-2b therapy for chronic hepatitis C

H. Mizusawa, M. Yamada, M. Yamawaki, 2001, Journal of neurology, neurosurgery, and psychiatry.

Brainstem congestion due to carotid-cavernous fistula via a shunt from the external carotid artery

H. Mizusawa, K. Ishikawa, T. Yokota, 2011, Journal of Neurology.

N. Saito, H. Mizusawa, Yosikazu Nakamura, 2013, BMJ Open.

Motor weakness and cerebellar ataxia in Sjögren syndrome—identification of antineuronal antibody: a case report

T. Uchihara, H. Mizusawa, S. Watabiki, 2002, Journal of the Neurological Sciences.

Recurrent aseptic meningitis: a new CSF complication of Sjogren’s syndrome

T. Uchihara, H. Mizusawa, K. Ishida, 2007, Journal of neurology.

Sequential changes in the non-coding control region sequences of JC polyomaviruses from the cerebrospinal fluid of patients with progressive multifocal leukoencephalopathy

T. Kanda, J. Kira, M. Saijo, 2012, Archives of Virology.

HTLV‐1‐associated Myelopathy/Tropical Spastic Paraparesis‐like Rats by Intravenous Injection of HTLV‐1‐producing Rabbit or Human T‐Cell Line into Adult WKA Rats

M. Miwa, H. Mizusawa, Hiroko Tanaka, 1993, Japanese journal of cancer research : Gann.

Chronic levodopa therapy enhances dopa absorption: Contribution to wearing-off

I. Kanazawa, H. Mizusawa, M. Murata, 2005, Journal of Neural Transmission.

Parkinsonism and Related Disorders

S. Orimo, H. Mizusawa, Masahiko Suzuki, 2012 .

Slowly progressive Foix–Chavany–Marie syndrome associated with chronic herpes simplex encephalitis

T. Kanda, H. Mizusawa, N. Sodeyama, 2002, Journal of neurology, neurosurgery, and psychiatry.

Spinocerebellar Ataxia Type 6 Mutation Alters P-type Calcium Channel Function*

Kinya Ishikawa, Shuta Toru, Toshiki Uchihara, 2000, The Journal of Biological Chemistry.

Delayed leukoencephalopathy after carbon monoxide poisoning presenting as subacute dementia.

Y. Sakurai, H. Mizusawa, S. Ishihara, 2014, Internal medicine.

Chronic inflammatory demyelinating polyradiculoneuropathy in a patient with Crohn's disease.

Mamoru Watanabe, H. Mizusawa, M. Nagahori, 2013, Internal medicine.

A neuropathological study of paraparetic rats injected with HTLV-I-producing T cells

M. Miwa, H. Mizusawa, Hiroko Tanaka, 1994, Journal of the Neurological Sciences.

Anti-GM1 antibody facilitates leakage in an in vitro blood–nerve barrier model

T. Kanda, H. Mizusawa, M. Yamawaki, 2000, Neurology.

FALS with Gly72Ser mutation in SOD1 gene: Report of a family including the first autopsy case

H. Akiyama, N. Shibata, H. Mizusawa, 2011, Journal of Neurological Sciences.

Early Detection of Abnormal Prion Protein in Genetic Human Prion Diseases Now Possible Using Real-Time QUIC Assay

I. Zerr, Yong-Sun Kim, H. Mizusawa, 2013, PloS one.

Title Ultrasensitive human prion detection in cerebrospinal fluid by real-timequaking-induced conversion

H. Mizusawa, M. Yamada, K. Satoh, 2017 .

[Role of lyrics and melody in song recognition: why is song recognition faster?].

H. Mizusawa, Yoko Saito, K. Ishii, 2009, Shinrigaku kenkyu : The Japanese journal of psychology.

Soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for differential diagnosis of mild cognitive impairment

S. Yoshida, H. Mizusawa, S. Murayama, 2021, Aging Clinical and Experimental Research.

Spinal cord ring enhancement in patients with neuromyelitis optica

K. Fujihara, H. Mizusawa, T. Yokota, 2015, Acta neurologica Scandinavica.

Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1.

I. Kanazawa, S. Tsuji, M. Miwa, 1997, American journal of human genetics.

Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias

H. Mitoma, S. Kakei, J. Honnorat, 2015, The Cerebellum.

Presynaptic dysfunction caused by cerebrospinal fluid from a patient with the ataxic form of Hashimoto's encephalopathy

H. Mitoma, F. Saitow, H. Mizusawa, 2014 .

Low-Titer Anti-GAD-Antibody-Positive Cerebellar Ataxia

H. Mitoma, H. Mizusawa, H. Niwa, 2013, The Cerebellum.

Selective suppression of cerebellar GABAergic transmission by an autoantibody to glutamic acid decarboxylase

H. Mitoma, Takayoshi Kobayashi, Si-young Song, 1999, Annals of neurology.

Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias

Shinji Kakei, Makoto Yoneda, Hiroshi Mitoma, 2015, The Cerebellum.

A case of Listeria meningitis associated with increased adenosine deaminase in cerebrospinal fluid.

H. Mizusawa, Y. Nishida, H. Komachi, 2007, Diagnostic microbiology and infectious disease.

Clinical, biochemical and molecular investigation of adult-onset glutaric acidemia type II: Characteristics in comparison with pediatric cases

T. Taketani, H. Mizusawa, A. Tamaoka, 2016, Brain and Development.

A case of dermatomyositis with rhabdomyolysis, rescued by intravenous immunoglobulin

N. Miyasaka, H. Mizusawa, F. Mizoguchi, 2015, Modern rheumatology.

Visualization of A beta 42(43) and A beta 40 in senile plaques with end-specific A beta monoclonals: evidence that an initially deposited species is A beta 42(43).

T. Iwatsubo, Y. Ihara, N. Nukina, 1994, Neuron.

Medical Procedures and Risk for Sporadic Creutzfeldt-Jakob Disease, Japan, 1999–2008

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Emerging infectious diseases.

Skeletal muscle MRI in complex regional pain syndrome.

T. Kanda, H. Mizusawa, T. Yokota, 2009, Internal medicine.

l-threo-3,4-dihydroxyphenylserine enhances the orthostatic responses of plasma renin activity and angiotensin II in multiple system atrophy

H. Mizusawa, S. Shoji, T. Yoshizawa, 1999, Journal of Neurology.

High incidence of HAM/TSP-like symptoms in WKA rats after administration of human T-cell leukemia virus type 1-producing cells

H. Tanaka, Yuetsu Tanaka, H. Mizusawa, 1994, Journal of virology.

Leftward movement in severe neglect

K. Seki, H. Mizusawa, S. Ishiai, 2000 .

Midkine inhibits apoptosis via extracellular signal regulated kinase (ERK) activation in PC12 cells.

M. Michikawa, H. Mizusawa, T. Muramatsu, 1999, Journal of medical and dental sciences.

Tandem internal models execute motor learning in the cerebellum

Soichi Nagao, Takeru Honda, Masao Ito, 2018, Proceedings of the National Academy of Sciences.

Vagus nerve palsy caused by varicella zoster virus infection without rash

M. Kawashima, H. Mizusawa, K. Ishikawa, 2007, Journal of Neurology.

Neuronal expression of the fukutin gene.

Y. Nakamura, M. Fukayama, H. Mizusawa, 2000, Human molecular genetics.

Silencing efficiency differs among tissues and endogenous microRNA pathway is preserved in short hairpin RNA transgenic mice

H. Mizusawa, M. Anzai, Hiroki Sasaguri, 2009, FEBS letters.

Intensity of chronic cerebral hypoperfusion determines white/gray matter injury and cognitive/motor dysfunction in mice

T. Kuroiwa, Haiyan Xu, H. Mizusawa, 2009, Journal of neuroscience research.

Presenilin-1 holoprotein is an interacting partner of sarco endoplasmic reticulum calcium-ATPase and confers resistance to endoplasmic reticulum stress.

P. S. St George-Hyslop, P. Fraser, T. Uchihara, 2010, Journal of Alzheimer's disease : JAD.

Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia

J. Inazawa, T. Amino, H. Mizusawa, 2007, Journal of Human Genetics.

On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1‐linked ADCA

H. Mizusawa, K. Ishikawa, 2006, Neuropathology : official journal of the Japanese Society of Neuropathology.

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor domains.

T. Mizutani, J. Kumagai, T. Amino, 2005, American journal of human genetics.

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan

I. Kanazawa, J. Inazawa, I. Imoto, 2003, Journal of Human Genetics.

Critical Contribution of Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand (Trail) to Apoptosis of Human Cd4+T Cells in HIV-1–Infected Hu-Pbl-Nod-Scid Mice

Mamoru Ito, Yuetsu Tanaka, N. Yamamoto, 2001, The Journal of experimental medicine.

Aβ1–40 but not Aβ1–42 levels in cortex correlate with apolipoprotein E ϵ4 allele dosage in sporadic Alzheimer's disease

S. Tsuji, M. Gearing, S. Mirra, 1997, Brain Research.

Developmental regulation of rat Ubc13 and Uev1B genes in the nervous system.

Hiroshi Takahashi, H. Mizusawa, Mutsufusa Watanabe, 2007, Gene expression patterns : GEP.

Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31

J. Taylor, K. Wada, C. E. Pearson, 2017, Neuron.

Serum amyloid A level is increased in neuromyelitis optica and atypical multiple sclerosis with smaller T2 lesion volume in brain MRI

T. Amino, H. Mizusawa, T. Kamata, 2013, Journal of Neuroimmunology.

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n.

Yuko Saito, Mari Yoshida, Fumitoshi Ishino, 2009, American journal of human genetics.

Intraperitoneal AAV9-shRNA inhibits target expression in neonatal skeletal and cardiac muscles.

H. Mizusawa, T. Shimada, T. Yokota, 2011, Biochemical and biophysical research communications.

R-spondin, a novel gene with thrombospondin type 1 domain, was expressed in the dorsal neural tube and affected in Wnts mutants.

M. Michikawa, H. Mizusawa, K. Katsube, 2004, Biochimica et biophysica acta.

CADASIL with a novel NOTCH3 mutation (Cys478Tyr).

H. Mizusawa, K. Ishikawa, K. Ozaki, 2015, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Distinct effects of caudalizing factors on regional specification of embryonic stem cell-derived neural precursors.

K. Mizuseki, Y. Sasai, H. Mizusawa, 2005, Brain research. Developmental brain research.

siRNA-based inhibition specific for mutant SOD1 with single nucleotide alternation in familial ALS, compared with ribozyme and DNA enzyme.

T. Hino, D. Bredesen, K. Taira, 2004, Biochemical and biophysical research communications.

Inhibition of intracellular hepatitis C virus replication by synthetic and vector‐derived small interfering RNAs

Mamoru Watanabe, Kazunari Taira, Li Yi, 2003, EMBO reports.

Introduction of short interfering RNA to silence endogenous E-selectin in vascular endothelium leads to successful inhibition of leukocyte adhesion.

M. Isobe, K. Taira, M. Miyagishi, 2003, Biochemical and biophysical research communications.

In vivo delivery of small interfering RNA targeting brain capillary endothelial cells.

T. Kanda, T. Hino, T. Terasaki, 2006, Biochemical and biophysical research communications.

A carbohydrate-binding protein, Galectin-1, promotes proliferation of adult neural stem cells.

T. Shimazaki, H. Okano, H. Nakauchi, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Efficient In Vivo Delivery of siRNA to the Liver by Conjugation of α-Tocopherol.

H. Mizusawa, T. Yokota, T. Kanouchi, 2008, Molecular therapy : the journal of the American Society of Gene Therapy.

Rimmed vacuolar distal myopathy

H. Mizusawa, Y. Toyokura, T. Mannen, 1987, Journal of Neurology.

Rimmed vacuolar distal myopathy: a clinical, electrophysiological, histopathological and computed tomographic study of seven cases

H. Mizusawa, Y. Toyokura, T. Mannen, 1987, Journal of Neurology.

Decreased expression of myotonic dystrophy protein kinase and disorganization of sarcoplasmic reticulum in skeletal muscle of myotonic dystrophy

Takayoshi Kobayashi, H. Ueda, H. Mizusawa, 1999, Journal of the Neurological Sciences.

Elevation of 8‐hydroxy‐2′‐deoxyguanosine in the cerebrospinal fluid of three patients with superficial siderosis

H. Mizusawa, A. Okawa, T. Hattori, 2015 .

Development of Purkinje cell degeneration in a knockin mouse model reveals lysosomal involvement in the pathogenesis of SCA6

C. Peters, M. Koike, Y. Uchiyama, 2012, Proceedings of the National Academy of Sciences.

Prospective 10-year surveillance of human prion diseases in Japan.

Y. Kuroiwa, M. Takeda, Y. Shiga, 2010, Brain : a journal of neurology.

Hypertrophic cranial pachymeningitis with spinal epidural granulomatous lesion.

H. Mizusawa, A. Matsumura, S. Shoji, 1995, Internal medicine.

[A case of Garcin's syndrome caused by pachymeningitis secondary to otitis media, responsive to antibiotic therapy].

I. Kanazawa, H. Mizusawa, N. Ohkoshi, 1991, Rinsho shinkeigaku = Clinical neurology.

Malignant hyperthermia in a patient with Becker muscular dystrophy: Dystrophin analysis and caffeine contracture study

H. Mizusawa, Y. Sugishita, S. Shoji, 1995, Neuromuscular Disorders.

Myotonic Dystrophy Protein Kinase Is a Sarcoplasmic Reticulum Protein Specifically Localized in Type I Muscle Fibers without Colocalization of SERCAII ATPase

Takayoshi Kobayashi, H. Ueda, H. Mizusawa, 2007 .

Six years’ accomplishment of the Initiative on Rare and Undiagnosed Diseases: nationwide project in Japan to discover causes, mechanisms, and cures

Y. Fukushima, T. Morio, H. Kurahashi, 2022, Journal of Human Genetics.

The carboxy-terminal fragment of α1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells

R. Dolmetsch, Hitoshi Takahashi, Fuminori Tsuruta, 2009, Acta Neuropathologica.

Characteristics of progressive multifocal leukoencephalopathy clarified through internet-assisted laboratory surveillance in Japan

M. Saijo, I. Kurane, H. Mizusawa, 2012, BMC Neurology.

Intraperitoneal administration of AAV9-shRNA inhibits target gene expression in the dorsal root ganglia of neonatal mice

H. Mizusawa, T. Shimada, T. Hirai, 2013, Molecular pain.

Intrathecal shRNA-AAV9 inhibits target protein expression in the spinal cord and dorsal root ganglia of adult mice.

H. Mizusawa, A. Okawa, K. Shinomiya, 2012, Human gene therapy methods.

Heterogeneity of Nigral and Cortical Lewy Bodies Differentiated by Amplified Triple-Labeling for Alpha-Synuclein, Ubiquitin, and Thiazin Red

S. Hirai, T. Mizutani, T. Uchihara, 2002, Experimental Neurology.

Immunopathology and Infectious Diseases NKT Cell-Dependent Amelioration of a Mouse Model of Multiple Sclerosis by Altering Gut Flora

T. Yamamura, H. Mizusawa, S. Miyake, 2010 .

Distal myopathy with rimmed vacuoles (DMRV)

I. Kanazawa, H. Mizusawa, J. Shimizu, 2004, Neurology.

[Tibial muscular dystrophy].

H. Mizusawa, 2001, Ryoikibetsu shokogun shirizu.

Rate of Complications Among the Recipients of Intrathecal Baclofen Pump in Japan: A Multicenter Study

T. Taira, Meigen Liu, Y. Katayama, 2013, Neuromodulation : journal of the International Neuromodulation Society.

Thyrotropin-Releasing Hormone-Induced Myoclonus and Tremor in a Patient With Hashimoto’s Encephalopathy

H. Mizusawa, K. Ishii, A. Tamaoka, 1995 .

Case Report: Thyrotropin‐Releasing Hormone‐Induced Myoclonus and Tremor in a Patient With Hashimoto's Encephalopathy

H. Mizusawa, K. Ishii, A. Tamaoka, 1995, The American journal of the medical sciences.

Spinocerebellar ataxia type 6 knockin mice develop a progressive neuronal dysfunction with age-dependent accumulation of mutant CaV2.1 channels

Masahiko Watanabe, R. Tsien, H. Zoghbi, 2008, Proceedings of the National Academy of Sciences.

Content of mutant mitochondrial DNA and organ dysfunction in a patient with a MELAS subgroup of mitochondrial encephalomyopathies

S. Ohta, H. Mizusawa, Y. Kagawa, 1993, Journal of the Neurological Sciences.

Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion

Steven J Collins, Masahito Yamada, H. Mizusawa, 2011, Nature Medicine.

Association of a polymorphism of the transforming growth factor-β1 gene with cerebral amyloid angiopathy

E. Otomo, Y. Itoh, H. Mizusawa, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Ataxin-3 Is Translocated into the Nucleus for the Formation of Intranuclear Inclusions in Normal and Machado–Joseph Disease Brains

S. Hirai, T. Uchihara, A. Nakamura, 2000, Experimental Neurology.

Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6.

I. Kanazawa, H. Mizusawa, S. Shoji, 1999, Human molecular genetics.

Binding of Pramipexole to Extrastriatal Dopamine D2/D3 Receptors in the Human Brain: A Positron Emission Tomography Study Using 11C-FLB 457

K. Ishii, K. Oda, K. Ishiwata, 2011, PloS one.

Delayed-onset ataxia in mice lacking α-tocopherol transfer protein: Model for neuronal degeneration caused by chronic oxidative stress

K. Jishage, H. Tomita, T. Uchihara, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: Dentatorubral‐pallidoluysian atrophy, machado‐joseph disease, and spinocerebellar ataxia type 1

I. Kanazawa, H. Mizusawa, J. Goto, 1997, Annals of neurology.

AJM300 (carotegrast methyl), an oral antagonist of α4-integrin, as induction therapy for patients with moderately active ulcerative colitis: a multicentre, randomised, double-blind, placebo-controlled, phase 3 study.

T. Hibi, H. Mizusawa, T. Ohmori, 2022, The lancet. Gastroenterology & hepatology.

AJM300 (Carotegrast Methyl), an Oral Antagonist of α4-Integrin, as Induction Therapy for Patients with Moderately Active Ulcerative Colitis: A Multicentre, Randomised, Double-Blind, Placebo-Controlled Phase 3 Study

T. Hibi, Mamoru Watanabe, H. Mizusawa, 2021, SSRN Electronic Journal.

Spreading of amyotrophic lateral sclerosis lesions—multifocal hits and local propagation?

Takayoshi Kobayashi, M. Nakagawa, S. Orimo, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Friedreich‐like ataxia with retinitis pigmentosa caused by the His101Gln mutation of the α‐Tocopherol transfer protein gene

M. Kiyosawa, T. Kanda, M. Arita, 1997, Annals of neurology.

[Malignant lymphoma presented as left trigeminal neuralgia].

H. Wakimoto, Daisuke Kobayashi, H. Mizusawa, 2009, Rinsho shinkeigaku = Clinical neurology.

[Prion disease--the characteristics and diagnostic points in Japan].

H. Mizusawa, N. Sanjo, 2010, Rinsho shinkeigaku = Clinical neurology.

MM2-type sporadic Creutzfeldt-Jakob disease: new diagnostic criteria for MM2-cortical type

H. Mizusawa, S. Murayama, Yosikazu Nakamura, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

The influence of PRNP polymorphisms on human prion disease susceptibility: an update

T. Shirai, H. Mizusawa, Y. Matsuura, 2015, Acta Neuropathologica.

Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases

H. Mizusawa, Yosikazu Nakamura, T. Kitamoto, 2022, Journal of Neurology, Neurosurgery, and Psychiatry.

Relationships between Clinicopathological Features and Cerebrospinal Fluid Biomarkers in Japanese Patients with Genetic Prion Diseases

Y. Shiga, H. Mizusawa, S. Murayama, 2013, PloS one.

Characterization of Sporadic Creutzfeldt-Jakob Disease and History of Neurosurgery to Identify Potential Iatrogenic Cases

H. Mizusawa, S. Murayama, Yosikazu Nakamura, 2020, Emerging infectious diseases.

Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease

T. Sato, Y. Shiga, H. Mizusawa, 2005, Neurology.

Preventive or promotive effects of PRNP polymorphic heterozygosity on the onset of prion disease

H. Mizusawa, T. Kitamoto, Hideaki Kai, 2023, Heliyon.

Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution

Y. Itoyama, K. Fujihara, T. Sato, 2007, Journal of Neurology.

Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation

H. Mizusawa, A. Shiraishi, M. Yamada, 2002, Journal of Neurology.

Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan

N. Saito, H. Mizusawa, Yosikazu Nakamura, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Dura mater graft‐associated Creutzfeldt‐Jakob disease in Japan: Clinicopathological and molecular characterization of the two distinct subtypes

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Clinical features and diagnosis of dura mater graft–associated Creutzfeldt–Jakob disease

T. Sato, H. Mizusawa, M. Noguchi-Shinohara, 2007, Neurology.

Coexistence of CJD and Alzheimer's disease: An autopsy case showing typical clinical features of CJD

H. Mizusawa, K. Ikeda, S. Watabiki, 2004, Neuropathology : official journal of the Japanese Society of Neuropathology.

Duration of Prion Disease is Longer in Japan Than in Other Countries

H. Mizusawa, Yosikazu Nakamura, M. Yamada, 2011, Journal of epidemiology.

Age at onset in genetic prion disease and the design of preventive clinical trials.

E. Minikel, S. Mead, J. Laplanche, 2019, Neurology.

Age of onset in genetic prion disease and the design of preventive clinical trials

E. Minikel, S. Mead, J. Laplanche, 2018, bioRxiv.

A Case of Creutzfeldt-Jakob Disease Presenting with Auditory Agnosia as an Initial Manifestation

S. Orimo, H. Mizusawa, R. Okeda, 2000, European Neurology.

Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene

H. Mizusawa, M. Yamada, T. Kitamoto, 2018, Prion.

Specific clinical signs and symptoms are predictive of clinical course in sporadic Creutzfeldt−Jakob disease

H. Mizusawa, S. Teramukai, M. Fukushima, 2016, European journal of neurology.

Diffusion-weighted magnetic resonance imaging in dura mater graft-associated Creutzfeldt-Jakob disease

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2020, Journal of the Neurological Sciences.

Creutzfeldt-Jakob disease after Jannetta’s operation with cadaveric dura mater graft: initial manifestations related to the grafted site

H. Mizusawa, M. Yamada, R. Okeda, 2002, Journal of Neurology.

Galectin-1 regulates neurogenesis in the subventricular zone and promotes functional recovery after stroke

H. Okano, T. Kuroiwa, H. Mizusawa, 2007, Experimental Neurology.

Degeneration of the thalamus and inferior olives associated with spongiform encephalopathy of the cerebral cortex.

I. Kanazawa, H. Mizusawa, N. Ohkoshi, 1988, Clinical neuropathology.

Geographic Difference of Mortality of Creutzfeldt-Jakob Disease in Japan

H. Mizusawa, Yosikazu Nakamura, M. Yamada, 2006, Journal of epidemiology.

[Prion disease surveillance in Japan: analysis of 1,241 patients].

H. Mizusawa, Yosikazu Nakamura, M. Noguchi-Shinohara, 2009, Rinsho shinkeigaku = Clinical neurology.

ApoE–ε4 and early–onset Alzheimer's

Ichiro Kanazawa, Osamu Onodera, Hitoshi Takahashi, 1994, Nature Genetics.

A Novel Form of Reversible Subacute Spongiform Leukoencephalopathy

S. Orimo, H. Mizusawa, E. Ozawa, 2001, European Neurology.

Developmental regulation of Ubc9 in the rat nervous system.

Kaoru Takahashi, Hiroshi Takahashi, H. Mizusawa, 2008, Acta biochimica Polonica.

The evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease

N. Hattori, H. Mizusawa, H. Yoshino, 2014, Neurobiology of Aging.

Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy

A. Kakita, Hitoshi Takahashi, H. Mizusawa, 2016, Acta Neuropathologica.

Comprehensive systematic review summary: Treatment of cerebellar motor dysfunction and ataxia

Ludger Schöls, Jeremy D Schmahmann, Tetsuo Ashizawa, 2018, Neurology.

Prism Adaptation Test (PAT): A Practical and Quantitative Method to Evaluate Cerebellar Function

H. Mizusawa, 2021, Contemporary Clinical Neuroscience.

A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan

S. Tsuji, G. Sobue, K. Nakashima, 2014, Orphanet Journal of Rare Diseases.

Thalamic involvement determined using VSRAD advance on MRI and easy Z-score analysis of 99mTc-ECD-SPECT in Gerstmann-Sträussler-Scheinker syndrome with P102L mutation

H. Matsuda, H. Mizusawa, Yuji Takahashi, 2017, Journal of the Neurological Sciences.

[Prion disease].

H. Mizusawa, 2010, Rinsho shinkeigaku = Clinical neurology.

[Prion disease].

H. Mizusawa, 2003, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Histological determination of nitric oxide synthase (NOS) and NADPH-diaphorase in ragged-red fibers from patients with mitochondrial encephalomyopathies

H. Mizusawa, S. Shoji, N. Ohkoshi, 1997, Journal of the Neurological Sciences.

Amino acid conditions near the GPI anchor attachment site of prion protein for the conversion and the GPI anchoring.

H. Mizusawa, T. Kitamoto, A. Kobayashi, 2010, Biochemical and biophysical research communications.

Lewy body-like inclusions in Onuf's nucleus from two cases of sporadic amyotrophic lateral sclerosis

H. Mizusawa, T. Kihira, S. Yoshida, 1993, Journal of the Neurological Sciences.

Efficacy of intravenous methylprednisolone pulse therapy in patients with multiple sclerosis and neuromyelitis optica

T. Kanda, K. Fujihara, J. Kira, 2016, Multiple sclerosis.

[Rapid progressive HTLV-1-associated myelopathy with bronchoalveolar lesions and a long spinal cord lesion extending to almost the entire spinal cord].

H. Mizusawa, Masaki Yamamoto, T. Yokota, 2011, Rinsho shinkeigaku = Clinical neurology.

Cerebrovascular lesions in acquired immune deficiency syndrome (AIDS)

H. Mizusawa, A. Hirano, M. Shintaku, 2004, Acta Neuropathologica.

Skein-like inclusions in the anterior horn cells in motor neuron disease

S. Yen, H. Mizusawa, A. Hirano, 1991, Journal of the Neurological Sciences.

UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase in nuclei and rimmed vacuoles of muscle fibers in DMRV (distal myopathy with rimmed vacuoles).

H. Mizusawa, S. Ishihara, F. Saito, 2008, Journal of medical and dental sciences.

[An autopsy case of HTLV-I associated myelopathy (HAM) with adult T-cell leukemia (ATL)].

I. Kanazawa, H. Mizusawa, T. Yazawa, 1990, Rinsho shinkeigaku = Clinical neurology.

Sural nerve biopsy in vasculitic neuropathies: morphometric analysis of the caliber of involved vessels.

E. Oguni, H. Mizusawa, S. Shoji, 1996, Journal of medicine.

Atherosclerosis is not implicated in association of APOE epsilon4 with AD.

M. Yamada, E. Otomo, Y. Itoh, 1999, Neurology.

Tyrosol Reduces Amyloid-β Oligomer Neurotoxicity and Alleviates Synaptic, Oxidative, and Cognitive Disturbances in Alzheimer's Disease Model Mice.

K. Wada, F. Kametani, M. Sekiguchi, 2019, Journal of Alzheimer's disease : JAD.

Association of presenilin-1 polymorphism with cerebral amyloid angiopathy in the elderly.

E. Otomo, Y. Itoh, H. Mizusawa, 1997, Stroke.

Altered Microstructure in Corticospinal Tract in Idiopathic Normal Pressure Hydrocephalus: Comparison with Alzheimer Disease and Parkinson Disease with Dementia

T Yuasa, S. Aoki, T. Yuasa, 2011, American Journal of Neuroradiology.

Impaired striatal dopamine release in homozygous Vps35 D620N knock-in mice.

Yuko Fujita, K. Hashimoto, H. Mizusawa, 2016, Human molecular genetics.

Pure pandysautonomia associated with interferon-alpha therapy

T. Kanda, H. Mizusawa, H. Yokote, 2007, Journal of Neurology.

Application of Laser Capture Microdissection to Periodontal Tissue

K. Ohya, H. Kondo, H. Mizusawa, 2007 .

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion

A. Vighetto, H. Wichmann, C. Duyckaerts, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Loss of MyD88 alters neuroinflammatory response and attenuates early Purkinje cell loss in a spinocerebellar ataxia type 6 mouse model

H. Mizusawa, Hiroshi Tanaka, K. Watase, 2015, Human molecular genetics.

Quantitative Evaluation of Human Cerebellum-Dependent Motor Learning through Prism Adaptation of Hand-Reaching Movement

Soichi Nagao, Takeru Honda, Takanori Yokota, 2015, PloS one.

Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease

I. Kanazawa, S. Tsuji, Hitoshi Takahashi, 1995, Nature Genetics.

DNA/RNA heteroduplex oligonucleotide for highly efficient gene silencing

K. Kataoka, H. Mizusawa, K. Miyata, 2015, Nature Communications.

Basement membrane-like matrix sponge for the three-dimensional proliferation culture of differentiated retinal horizontal interneurons.

Kazunori Nakajima, Itsuki Ajioka, S. Ichinose, 2011, Biomaterials.

Studies on neurotransmitter markers and neuronal cell density in the cerebellar system in olivopontocerebellar atrophy and cortical cerebellar atrophy

I. Kanazawa, N. Nukina, H. Mizusawa, 1985, Journal of the Neurological Sciences.

Transgenic Small Interfering RNA Halts Amyotrophic Lateral Sclerosis in a Mouse Model*

K. Taira, M. Miyagishi, H. Mizusawa, 2005, Journal of Biological Chemistry.

Discrepancy between tau immunoreactivity and argyrophilia by the Bodian method in neocortical neurons of corticobasal degeneration

T. Uchihara, H. Mizusawa, K. Ikeda, 1998, Acta Neuropathologica.

Potential value of soluble APPα and APPβ in CSF as biomarkers of dementia disorders: Unresolved issues and perspectives

H. Mizusawa, W. Araki, Y. Araki, 2018, Neurology and Clinical Neuroscience.

Re-evaluation of soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for early diagnosis of dementia disorders

K. Ishii, H. Matsuda, K. Arima, 2017, Biomarker Research.

Enhanced Phospholipase A2 Group 3 Expression by Oxidative Stress Decreases the Insulin-Degrading Enzyme

H. Mizusawa, S. Murayama, K. Ishikawa, 2015, PloS one.

Visual Reproduction on the Wechsler Memory Scale-Revised as a Predictor of Alzheimer’s Disease in Japanese Patients with Mild Cognitive Impairments

M. Tomita, H. Mizusawa, N. Sanjo, 2013, Dementia and Geriatric Cognitive Disorders.

Recurrent breast cancer with metastatic brachial plexopathy.

H. Mizusawa, T. Irioka, 2010, Internal medicine.

Three‐Layered Structure Shared Between Lewy Bodies and Lewy Neurites—Three‐Dimensional Reconstruction of Triple‐Labeled Sections

T. Uchihara, A. Nakamura, S. Orimo, 2008, Brain pathology.

A Score for Predicting Paroxysmal Atrial Fibrillation in Acute Stroke Patients: iPAB Score.

Kosuke Watanabe, M. Tomita, H. Mizusawa, 2015, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

H. Mizusawa, Y. Koyanagi, Yoshiharu Miura, 2003, Journal of medical and dental sciences.

Pattern of epitopic reactivity of the anti-Hu antibody on HuD with and without paraneoplastic syndrome

H. Mizusawa, K. Jaeckle, A. Azuma, 1999, Journal of neurology, neurosurgery, and psychiatry.

Intrathecal AAV serotype 9-mediated delivery of shRNA against TRPV1 attenuates thermal hyperalgesia in a mouse model of peripheral nerve injury.

M. Tominaga, H. Mizusawa, A. Okawa, 2014, Molecular therapy : the journal of the American Society of Gene Therapy.

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6

T. Tsutsumi, H. Mizusawa, S. Shoji, 2004, Journal of Human Genetics.

Pale Neurites, Premature α‐Synuclein Aggregates with Centripetal Extension from Axon Collaterals

T. Uchihara, A. Nakamura, S. Orimo, 2012, Brain pathology.

Glycaemic control boosts glucosylated nanocarrier crossing the BBB into the brain

Y. Anraku, K. Toh, Y. Matsumoto, 2017, Nature Communications.

Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians

M. Vidailhet, A. Vighetto, T. Illig, 2011, Neurology.

The chromosome 16q‐linked autosomal dominant cerebellar ataxia (16q‐ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell

H. Mizusawa, K. Ishikawa, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III

T. Arinami, H. Mizusawa, I. Kondo, 2005, Neurology.

Impaired Adaptive Motor Learning Is Correlated With Cerebellar Hemispheric Gray Matter Atrophy in Spinocerebellar Ataxia Patients: A Voxel-Based Morphometry Study

T. Hanakawa, H. Mizusawa, Yuji Takahashi, 2019, Front. Neurol..

When should we test patients with familial ataxias for SCA31? A misdiagnosed condition outside Japan?

O. Barsottini, S. Raskin, H. Mizusawa, 2015, Journal of the Neurological Sciences.

A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxia

T. Yamawaki, H. Mizusawa, S. Shoji, 2000, Neurology.

[Overcoming neurological diseases-breakthrough for new era].

H. Mizusawa, 2013, Rinsho shinkeigaku = Clinical neurology.

The 50th Anniversary of Japanese Society of Neuropathology Memorial Symposium: Milestones in Neuropathology from Japanneup_1142

H. Mizusawa, K. Ishikawa, 2010 .

Pathology of the dentate nucleus in progressive supranuclear palsy: a histological, immunohistochemical and ultrastructural study

A. Hirano, S. Yen, H. Mizusawa, 2004, Acta Neuropathologica.

Marked hypertrophy of the cauda equina in a patient with chronic inflammatory demyelinating polyradiculoneuropathy presenting as lumbar stenosis

T. Kanda, H. Mizusawa, T. Tsunemi, 2005, Journal of neurology.

Unmyelinated nerve fibers in sural nerve in pure autonomic failure

T. Kanda, H. Mizusawa, T. Yokota, 1998, Annals of neurology.

Senile Dementia of the Neurofibrillary Tangle Type: A Comparison with Alzheimer’s Disease

E. Otomo, Y. Itoh, H. Mizusawa, 2001, Dementia and Geriatric Cognitive Disorders.

Nuclear bridges within multinucleated giant cells in subacute encephalitis of acquired immune deficiency syndrome (AIDS)

H. Mizusawa, A. Hirano, A. Hirano, 2004, Acta Neuropathologica.

High voltage electrical stimulation of the proximal hypoglossal nerve in normal subjects

H. Mizusawa, T. Yokota, T. Kanouchi, 2002, Clinical Neurophysiology.

[Bilateral medial medullary infarction presented with monoplegia of the lower limb, followed by paraplegia and finally by tetraplegia].

T. Kanda, T. Hino, H. Mizusawa, 2003, Rinsho shinkeigaku = Clinical neurology.

Analysis of the Adrenal Gland Is Useful for Evaluating Pathology of the Peripheral Autonomic Nervous System in Lewy Body Disease

T. Iwatsubo, M. Fukayama, H. Mizusawa, 2007, Journal of neuropathology and experimental neurology.

Regional analysis of age‐related decline in dopamine transporters and dopamine D2‐like receptors in human striatum

K. Ishii, K. Oda, K. Ishiwata, 2009, Synapse.

Close association of water channel AQP1 with amyloid-β deposition in Alzheimer disease brains

J. Satoh, K. Arima, H. Mizusawa, 2008, Acta Neuropathologica.

Epidemiologic Features of Human Prion Diseases in Japan: A Prospective 14-year Surveillance.

K. Kotani, H. Mizusawa, M. Yamada, 2014 .

α2-Macroglobulin polymorphism is not associated with AD or AD-type neuropathology in the Japanese

M. Yamada, E. Otomo, Y. Itoh, 2000, Neurology.

Disease-specific monoclonal antibodies targeting glutamate decarboxylase impair GABAergic neurotransmission and affect motor learning and behavioral functions

H. Mitoma, Y. Yanagawa, J. Delgado-García, 2015, Front. Behav. Neurosci..

The professional practice and training of neurology in the Asian and Oceanian Region: A cross-sectional survey by the Asian and Oceanian Association of Neurology (AOAN)

N. Bornstein, M. Wasay, M. Mehndiratta, 2017, Journal of the Neurological Sciences.

Nationwide Laboratory Surveillance of Progressive Multifocal Leukoencephalopathy in Japan: Fiscal Years 2011–2020

H. Ebihara, K. Mori, N. Funata, 2023, Viruses.

Metastatic CNS lymphoma presenting with periventricular dissemination — MRI and neuropathological findings in an autopsy case

H. Akiyama, H. Mizusawa, J. Goto, 2009, Journal of the Neurological Sciences.

Dissection of the polygenic architecture of neuronal Aβ production using a large sample of individual iPSC lines derived from Alzheimer’s disease patients

Keith A. Johnson, Raymond Scott Turner, Charles D. Smith, 2022, Nature Aging.

Aging of the human limbic system: Observations of centenarian brains and analyses of genetic risk factors for senile changes

E. Otomo, Y. Itoh, H. Mizusawa, 1998 .

[Optic nerve swelling and gadolinium contrast enhancement on magnetic resonance imaging in the subacute stage of Leber's hereditary optic neuropathy: a case report].

H. Mizusawa, K. Ishikawa, T. Yokota, 2012, Rinsho shinkeigaku = Clinical neurology.

Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases

M. Mimura, K. Arima, H. Akiyama, 2005, Acta Neuropathologica.

Human neural stem/progenitor cells, expanded in long‐term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils

T. Shimazaki, H. Okano, T. Kuroiwa, 2004, Journal of neuroscience research.

18F-FDG PET successfully detects spinal cord sarcoidosis

H. Mizusawa, T. Tsunemi, T. Irioka, 2009, Journal of Neurology.

Efficient generation of mature cerebellar Purkinje cells from mouse embryonic stem cells

T. Shimazaki, H. Okano, M. Yuzaki, 2010, Journal of neuroscience research.

Intractable hiccup caused by medulla oblongata lesions: A study of an autopsy patient with possible neuromyelitis optica

H. Akiyama, T. Uchihara, A. Nakamura, 2009, Journal of the Neurological Sciences.

Differentiating between progressive supranuclear palsy and corticobasal degeneration by brain perfusion SPET

H. Mizusawa, H. Shibuya, Y. Murata, 2001, Nuclear medicine communications.

Efficacy and safety of leuprorelin in patients with spinal and bulbar muscular atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial

S. Tsuji, G. Sobue, M. Morita, 2010, The Lancet Neurology.

Postmortem study of ataxia with retinitis pigmentosa by mutation of the α-tocopherol transfer protein gene

M. Kiyosawa, J. Kumagai, T. Uchihara, 2000, Journal of neurology, neurosurgery, and psychiatry.

Tacrolimus Monotherapy: A Promising Option for Ocular Myasthenia Gravis

H. Mizusawa, T. Yokota, N. Sanjo, 2013, European Neurology.

Presenilin-1 holoprotein is an interacting partner of sarco endoplasmic reticulum calcium-ATPase and confers resistance to endoplasmic reticulum stress

P. Fraser, P. George-Hyslop, T. Uchihara, 2010, Alzheimer's & Dementia.

[Distal myopathy with rimmed vacuoles].

H. Mizusawa, 2001, Ryoikibetsu shokogun shirizu.

Autonomic dysfunction and orthostatic hypotention caused by vitamin B12 deficiency

H. Mizusawa, T. Yokota, S. Toru, 1999, Journal of Neurology Neurosurgery & Psychiatry.

Efficient in vivo delivery of siRNA to the liver by conjugation of alpha-tocopherol.

H. Mizusawa, T. Yokota, T. Kanouchi, 2008, Molecular therapy : the journal of the American Society of Gene Therapy.

Down regulation of DJ-1 enhances cell death by oxidative stress, ER stress, and proteasome inhibition.

H. Ariga, R. Takahashi, H. Mizusawa, 2003, Biochemical and biophysical research communications.

Sera from Guillain-Barré patients enhance leakage in blood–nerve barrier model

T. Kanda, H. Mizusawa, M. Yamawaki, 2003, Neurology.

A Deletion Polymorphism of α2-Macroglobulin Gene and Cerebral Amyloid Angiopathy

E. Otomo, Y. Itoh, H. Mizusawa, 1999 .

Autosomal dominant pure cerebellar ataxia. A clinical and genetic analysis of eight Japanese families.

I. Kanazawa, S. Tsuji, H. Mizusawa, 1996, Brain : a journal of neurology.

Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6)

I. Kanazawa, H. Mizusawa, S. Shoji, 1999, Journal of neurology, neurosurgery, and psychiatry.

Antihistamine‐associated myoclonus: A case report

H. Mizusawa, T. Yokota, T. Irioka, 2008, Movement disorders : official journal of the Movement Disorder Society.

Focal accumulation of phosphorylated neurofilaments within anterior horn cell in familial amyotrophic lateral sclerosis

S. Yen, H. Mizusawa, A. Hirano, 2004, Acta Neuropathologica.

A sporadic case of late-onset familial amyloid polyneuropathy with Bence-Jones proteinuria

H. Mizusawa, T. Furuya, M. Yamada, 1999, Journal of Neurology.

Characteristic changes in T2-value, apparent diffusion coefficient, and ultrastructure of substantia nigra evolving exofocal postischemic neuronal death in rats

T. Nagaoka, N. Miyasaka, T. Kuroiwa, 2001, Brain Research.

Glucose hypometabolism in medial frontal cortex of patients with apraxia of lid opening

M. Kiyosawa, M. Senda, K. Ishii, 2003, Graefe's Archive for Clinical and Experimental Ophthalmology.

Three-repeat Tau 69 is a major tau isoform in laser-microdissected Pick bodies

K. Arima, K. Kaneko, Hitoshi Takahashi, 2006, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Longitudinal analysis of risk factors for dementia based on Mild Cognitive Impairment Screen results and questionnaire responses from healthy Japanese individuals registered in an online database

H. Matsuda, H. Shimada, H. Mizusawa, 2019, Alzheimer's & dementia.

A case of cluster headache associated with mitochondrial DNA deletions

H. Mizusawa, A. Tamaoka, M. Odawara, 1997, Muscle & nerve.

Dropped head in polymyositis

Takayoshi Kobayashi, H. Mizusawa, T. Yokota, 2012, Rheumatology International.

Spinocerebellar ataxia type 6 (SCA 6)

H. Mizusawa, Hidehiro Mizusawa, 1998, Neuroscience Research.

Proximal motor conduction evaluated by transcranial magnetic stimulation in acquired inflammatory demyelinating neuropathies

H. Mizusawa, T. Yokota, A. Inaba, 2001, Clinical Neurophysiology.

The effect of 3,4-diaminopyridine on the patients with hereditary pure cerebellar ataxia

H. Mizusawa, T. Tsunemi, K. Ishikawa, 2010, Journal of the Neurological Sciences.

Fatal encephalitis in a case of hypereosinophilic syndrome: MRI and autopsy findings.

H. Akiyama, H. Mizusawa, O. Yokota, 2011, Internal medicine.

Temporal Relationship between Impairment of Cerebellar Motor Learning and Deterioration of Ataxia in Patients with Cerebellar Degeneration.

S. Nagao, H. Mizusawa, K. Ishikawa, 2023, Cerebellum.

Reversibility of cerebellar GABAergic synapse impairment induced by anti-glutamic acid decarboxylase autoantibodies

H. Mitoma, H. Mizusawa, K. Ishida, 2008, Journal of the Neurological Sciences.

Dual impairment of GABAA- and GABAB-receptor-mediated synaptic responses by autoantibodies to glutamic acid decarboxylase

H. Mitoma, H. Mizusawa, M. Shizuka-Ikeda, 2003, Journal of the Neurological Sciences.

Re-evaluation of soluble APP-α and APP-β in cerebrospinal fluid as potential biomarkers for early diagnosis of dementia disorders

K. Ishii, H. Matsuda, K. Arima, 2017, Biomarker Research.

Increased CSF tau protein in corticobasal degeneration

T. Uchihara, H. Mizusawa, H. Mori, 1997, Journal of Neurology.

Chiasmal optic neuritis following mumps parotitis

H. Mizusawa, K. Nakao, T. Yokota, 2008, Journal of Neurology.

Iatrogenic Creutzfeldt-Jakob disease.

H. Mizusawa, T. Kitamoto, A. Kobayashi, 2018, Handbook of clinical neurology.

[Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) associated with hypothalamo-pituitary hypofunction--a case report].

I. Kanazawa, H. Mizusawa, N. Ohkoshi, 1991, Rinsho shinkeigaku = Clinical neurology.

Multiple sclerosis and neuromyelitis optica spectrum disorders: some similarities in two distinct diseases

H. Mizusawa, H. Yokote, 2016, Neural regeneration research.

New RNAi strategy for selective suppression of a mutant allele in polyglutamine disease.

H. Mizusawa, K. Ishikawa, T. Yokota, 2005, Oligonucleotides.

Transplantation of neuronal cells induced from human mesenchymal stem cells improves neurological functions after stroke without cell fusion

I. Sekiya, T. Muneta, Haiyan Xu, 2010, Journal of neuroscience research.

Presenilin 1 intronic polymorphism is not associated with Alzheimer type neuropathological changes or sporadic Alzheimer’s disease

E. Otomo, Y. Itoh, H. Mizusawa, 1998, Journal of neurology, neurosurgery, and psychiatry.

Lack of Genetic Associations of Alpha-1-Antichymotrypsin Polymorphism with Alzheimer-Type Neuropathological Changes or Sporadic Alzheimer’s Disease

E. Otomo, Y. Itoh, H. Mizusawa, 1999, Dementia and Geriatric Cognitive Disorders.

Novel Cav2.1 Splice Variants Isolated from Purkinje Cells Do Not Generate P-type Ca2+ Current*

H. Mizusawa, H. Saegusa, T. Tanabe, 2002, The Journal of Biological Chemistry.

Transition of areas of eosinophilic neurons and reactive astrocytes to delayed cortical infarcts after transient unilateral forebrain ischemia in Mongolian gerbils

T. Kuroiwa, H. Mizusawa, N. Katsumata, 2005, Acta Neuropathologica.

Distal hyperintense vessels on FLAIR images predict large-artery stenosis in patients with transient ischemic attack

H. Mizusawa, A. Shiraishi, T. Yokota, 2013, Neuroradiology.

ORANGE's challenge: developing wide-ranging dementia research in Japan

T. Sakurai, Keisuke Suzuki, H. Mizusawa, 2016, The Lancet Neurology.

[Reflex sympathetic dystrophy secondary to lumbar disk herniation].

H. Mizusawa, A. Tamaoka, S. Shoji, 1994, Rinsho shinkeigaku = Clinical neurology.

Validation of cardiac 123I-MIBG scintigraphy in patients with Parkinson’s disease who were diagnosed with dopamine PET

K. Ishii, K. Oda, K. Ishiwata, 2009, European Journal of Nuclear Medicine and Molecular Imaging.

Association of neprilysin polymorphism with cerebral amyloid angiopathy

M. Yamada, E. Otomo, Y. Itoh, 2003, Journal of neurology, neurosurgery, and psychiatry.

A Japanese family with spinocerebellar ataxia type 6 which includes three individuals homozygous for an expanded CAG repeat in the SCA6/CACNL1A4 gene

H. Mizusawa, M. Nishizawa, Y. Takiyama, 1998, Journal of the Neurological Sciences.

A diagnostic decision tree for adult cerebellar ataxia based on pontine magnetic resonance imaging

M. Tomita, H. Mizusawa, T. Hattori, 2018, Journal of the Neurological Sciences.

High-dose ubiquinol supplementation in multiple-system atrophy: a multicentre, randomised, double-blinded, placebo-controlled phase 2 trial

N. Sawamoto, T. Matsukawa, R. Hanajima, 2023, EClinicalMedicine.

Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants

O. Migita, N. Matsumoto, M. Iwasaki, 2023, Brain and Development.

[Anti-VGKC antibody-associated limbic encephalitis/Morvan syndrome].

H. Mizusawa, T. Misawa, 2010, Brain and nerve = Shinkei kenkyu no shinpo.

Efficient in vivo delivery of antisense oligonucleotide to choroid plexus.

H. Mizusawa, T. Yokota, H. Kuwahara, 2013, Journal of medical and dental sciences.

Extrapyramidal motor symptoms versus striatal infarction volume after focal ischemia in mongolian gerbils

S Endo, T. Kuroiwa, H. Mizusawa, 2004, Neuroscience.

Neurological Dysfunctions Versus Regional Infarction Volume After Focal Ischemia in Mongolian Gerbils

T. Kuroiwa, H. Mizusawa, R. Okeda, 2003, Stroke.

Cerebrospinal fluid metabolite and nigrostriatal dopaminergic function in Parkinson’s disease

K. Oda, K. Ishiwata, H. Mizusawa, 2009, Acta neurologica Scandinavica.

Atypical FTLD‐FUS associated with ALS‐TDP: A case report

H. Akiyama, H. Mizusawa, O. Yokota, 2013, Neuropathology : official journal of the Japanese Society of Neuropathology.

Efficacy of methylprednisolone pulse therapy for acute relapse in Japanese patients with multiple sclerosis and neuromyelitis optica: A multicenter retrospective analysis – 1. Whole group analysis

T. Kanda, K. Fujihara, J. Kira, 2013 .

Ubiquitinated alpha B-crystallin in glial cytoplasmic inclusions from the brain of a patient with multiple system atrophy.

H. Mizusawa, H. Mori, A. Tamaoka, 1995, Journal of the neurological sciences.

Dose‐dependent association of apolipoprotein e allele ε4 with late‐onset, sporadic Alzheimer's disease

E. Oguni, T. Arinami, H. Mizusawa, 1994 .

Butyrylcholinesterase K variant and cerebral amyloid angiopathy.

E. Otomo, Y. Itoh, H. Mizusawa, 1998, Stroke.

Analysis of risk factors for mild cognitive impairment based on word list memory test results and questionnaire responses in healthy Japanese individuals registered in an online database

H. Matsuda, H. Shimada, H. Mizusawa, 2018, PLoS ONE.

Opsoclonus caused by diphenhydramine self-poisoning.

H. Mizusawa, N. Uchida, M. Iwase, 2009, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

The familial occurrence may give a clue to the pathogenesis of inclusion body myositis.

H. Mizusawa, 2003, Internal medicine.

Ultrastructural and MRI study of the substantia nigra evolving exofocal post‐ischemic neuronal death in the rat

T. Nagaoka, N. Miyasaka, T. Kuroiwa, 2002, Neuropathology : official journal of the Japanese Society of Neuropathology.

Somatosensory‐evoked cortical potential during attacks of paroxysmal dysesthesia in multiple sclerosis

H. Mizusawa, T. Yokota, T. Kanouchi, 2005, European journal of neurology.

Transplantation of human neural stem/progenitor cells overexpressing galectin-1 improves functional recovery from focal brain ischemia in the mongolian gerbil

H. Okano, K. Sawamoto, Y. Toyama, 2011, Molecular Brain.

High-density lipoprotein facilitates in vivo delivery of α-tocopherol-conjugated short-interfering RNA to the brain.

H. Mizusawa, K. Miyata, T. Yokota, 2011, Human gene therapy.

Intramedullary spinal cord metastasis with a longitudinally extensive spinal cord lesion.

H. Mizusawa, T. Irioka, K. Soga, 2011, Internal medicine.

Ischemic stroke in a young adult with Turner syndrome

H. Mizusawa, T. Irioka, 2011, Neurological Sciences.

Gluten Ataxia in Japan

H. Mitoma, H. Mizusawa, M. Ihara, 2014, The Cerebellum.

Hemorrhagic bulla in Churg-Strauss syndrome.

H. Mizusawa, T. Irioka, 2011, Internal medicine.

A deletion polymorphism of alpha(2)-macroglobulin gene and cerebral amyloid angiopathy.

E. Otomo, Y. Itoh, H. Mizusawa, 1999, Stroke.

Time profile of eosinophilic neurons in the cortical layers and cortical atrophy.

T. Kuroiwa, H. Mizusawa, N. Katsumata, 2006, Acta neurochirurgica. Supplement.

Brain perfusion SPECT in patients with corticobasal degeneration: Analysis using statistical parametric mapping

Y. Okubo, E. Matsushima, H. Mizusawa, 2003, Movement disorders : official journal of the Movement Disorder Society.

Assessment and Rating of Motor Cerebellar Ataxias With the Kinect v2 Depth Sensor: Extending Our Appraisal

H. Mitoma, T. Hanakawa, S. Kakei, 2020, Frontiers in Neurology.

Primary ocular and central nervous system malignant lymphoma first manifested as uveitis: possible role of single photon emission computed tomography with N-isopropyl-123I-p-iodoamphetamine in the diagnostic procedure.

H. Kojima, H. Mizusawa, S. Shoji, 1994, Internal medicine.

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.

[Spinocerebellar ataxia type 6].

H. Mizusawa, K. Ishikawa, 2001, Clinical calcium.

[A case of Hashimoto's encephalopathy with a relapsing course related to menstrual cycle].

H. Mizusawa, K. Ishii, A. Tamaoka, 1993, Rinsho shinkeigaku = Clinical neurology.

Electrophysiological evaluation of conduction in the most proximal motor root segment

H. Mizusawa, T. Yokota, A. Inaba, 2002, Muscle & nerve.

FUS regulates RAN translation through modulating the G-quadruplex structure of GGGGCC repeat RNA in C9orf72-linked ALS/FTD

H. Taguchi, L. Petrucelli, K. Nakatani, 2023, bioRxiv.

A novel neurotrophic pyrimidine compound MS‐818 enhances neurotrophic effects of basic fibroblast growth factor

Takayoshi Kobayashi, A. Awaya, M. Michikawa, 1998, Journal of neuroscience research.

123I-metaiodobenzylguanidine myocardial scintigraphy in Parkinson’s disease

S. Orimo, H. Mizusawa, T. Sugimoto, 1999, Journal of neurology, neurosurgery, and psychiatry.

Long-term cognitive and neuropsychological symptoms after global cerebral ischemia in Mongolian gerbils.

T. Kuroiwa, H. Mizusawa, N. Katsumata, 2006, Acta neurochirurgica. Supplement.

MATTERS ARISING

H. Mizusawa, S. Shoji, N. Ohkoshi, 1995 .

FGF-9 is an autocrine/paracrine neurotrophic substance for spinal motoneurons

T. Kanda, H. Mizusawa, T. Kurokawa, 1999, International Journal of Developmental Neuroscience.

Peripheral neuropathy of mitochondrial myopathies.

I. Kanazawa, H. Mizusawa, N. Ohkoshi, 1991, Revue neurologique.

[Pneumatosis intestinalis in a patient of myasthenia gravis treated with high-dose corticosteroid].

T. Kanda, H. Mizusawa, K. Kameyama, 2003, Rinsho shinkeigaku = Clinical neurology.

Survey of Subacute Sclerosing Panencephalitis in Japan

M. Mizuguchi, Yasuhiro Suzuki, M. Hosoya, 2012, Journal of child neurology.

A case of cluster headache associated with mitochondrial DNA deletions

H. Mizusawa, A. Tamaoka, M. Odawara, 1997, Muscle & nerve.

Skeletal anomaly and opisthotonus in early-onset epileptic encephalopathy with KCNQ2 abnormality

N. Matsumoto, H. Mizusawa, S. Miyatake, 2023, Brain and Development.

16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

H. Shimazaki, T. Amino, H. Mizusawa, 2006, Journal of the Neurological Sciences.

Relationship and factor structure in multisystem neurodegeneration in Parkinson's disease

M. Hallett, S. Orimo, H. Mizusawa, 2014, Acta neurologica Scandinavica.

Genome-wide identification of tandem repeats associated with splicing variation across 49 tissues in humans

K. Misawa, N. Matsumoto, H. Mizusawa, 2023, Genome research.

Glycaemic control boosts glucosylated nanocarrier crossing the BBB into the brain

Y. Anraku, K. Toh, Y. Matsumoto, 2017, Nature Communications.

Bilateral facial nerve palsy caused by a metastatic malignant lymphoma.

H. Mizusawa, K. Ozaki, T. Irioka, 2011, Internal medicine.

Parkinson's Disease: The Dirty Truth About the Air – Authors' Reply

H. Mizusawa, Y. Saitoh, 2022, Annals of Indian Academy of Neurology.

Teaching NeuroImages: Reversible cognitive impairment with bithalamic lesions caused by a dural arteriovenous fistula

Y. Yoshino, H. Mizusawa, S. Nemoto, 2013, Neurology.

Hemichorea improved by extracranial–intracranial bypass surgery for middle cerebral artery occlusion

H. Mizusawa, J. Ayabe, T. Irioka, 2010, Journal of Neurology.

Significant increase in the expression of matrix metalloproteinase 7 in primary CNS lymphoma

Kikuo Ohno, Maki Hasegawa, Jiro Kumagai, 2008, Neuropathology : official journal of the Japanese Society of Neuropathology.

Abeta1-40 but not Abeta1-42 levels in cortex correlate with apolipoprotein E epsilon4 allele dosage in sporadic Alzheimer's disease.

P. S. St George-Hyslop, S. Tsuji, M. Gearing, 1997, Brain research.

Genetic Creutzfeldt‒Jakob disease with 5-octapeptide repeats presented as frontotemporal dementia

H. Mizusawa, F. Moriwaka, K. Satoh, 2023, Human Genome Variation.

MELAS with prominent white matter gliosis and atrophy of the cerebellar granular layer: a clinical, genetic, and pathological study

H. Mizusawa, K. Ikeda, K. Tsuchiya, 1999, Acta Neuropathologica.

Increase of disease duration of amyotrophic lateral sclerosis in a mouse model by transgenic small interfering RNA.

H. Mizusawa, Yuki Yamamoto, M. Anzai, 2007, Archives of neurology.

Rate of Complications Among the Recipients of Intrathecal Baclofen Pump in Japan: A Multicenter Study

T. Taira, Meigen Liu, Y. Katayama, 2013, Neuromodulation : journal of the International Neuromodulation Society.

シンポジウム16―5 神経疾患とRNA SCA31（脊髄小脳失調症31型）

T. Amino, H. Mizusawa, K. Ishikawa, 2010 .

Alternative splicing in the C-terminal tail of Cav2.1 is essential for preventing a neurological disease in mice

Masahiko Watanabe, M. Kano, T. Miyazaki, 2017, Journal of the Neurological Sciences.

Dissection of the polygenic architecture of neuronal Aβ production using a large sample of individual iPSC lines derived from Alzheimer’s disease patients

Sterling C. Johnson, Keith A. Johnson, Raymond Scott Turner, 2022, Nature Aging.

Two region‐dependent pathways of eosinophilic neuronal death after transient cerebral ischemia

T. Kuroiwa, Haiyan Xu, H. Mizusawa, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Spreading of amyotrophic lateral sclerosis lesions—multifocal hits and local propagation?

H. Mizusawa, K. Shibuya, S. Misawa, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

No association of paraoxonase gene polymorphism with atherosclerosis or Alzheimer’s disease

M. Yamada, E. Otomo, Y. Itoh, 1999, Neurology.

Cerebral cortical pathology of sporadic olivopontocerebellar atrophy

Ichiro Kanazawa, I. Kanazawa, H. Mizusawa, 1993, Journal of the Neurological Sciences.

The professional practice and training of neurology in the Asian and Oceanian Region: A cross-sectional survey by the Asian and Oceanian Association of Neurology (AOAN)

N. Bornstein, M. Wasay, M. Mehndiratta, 2017, Journal of the Neurological Sciences.

Intractable hiccup caused by medulla oblongata lesions: A study of an autopsy patient with possible neuromyelitis optica

H. Akiyama, T. Uchihara, A. Nakamura, 2009, Journal of the Neurological Sciences.

[Case of an 81-year-old woman with theophylline-associated seizures followed by partial seizures due to vitamin B6 deficiency].

H. Mizusawa, H. Kuwahara, A. Inaba, 2008, Rinsho shinkeigaku = Clinical neurology.

Peroxiredoxin I (macrophage 23 kDa stress protein) is highly and widely expressed in the rat nervous system

H. Mizusawa, T. Ishii, S. Bannai, 2000, Neuroscience Letters.

Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects

H. Mizusawa, K. Ishikawa, T. Yokota, 2017, Journal of the Neurological Sciences.

Nuclear bridges in multinucleated giant cells associated with primary lymphoma of the brain in acquired immune deficiency syndrome (AIDS)

H. Mizusawa, T. Kato, A. Hirano, 2004, Acta Neuropathologica.

Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene.

H. Mizusawa, N. Sanjo, F. Furukawa, 2014, JAMA neurology.

A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano.

Y. Fukushima, N. Matsumoto, Kunihiro Yoshida, 2006, Journal of human genetics.

Efficient in vivo delivery of antisense oligonucleotide to choroid plexus.

H. Mizusawa, T. Yokota, H. Kuwahara, 2013, Journal of medical and dental sciences.

Presynaptic inhibition of cerebellar GABAergic transmission by glutamate decarboxylase autoantibodies in progressive cerebellar ataxia

H. Mitoma, Si-young Song, M. Shoji, 2001, Journal of neurology, neurosurgery, and psychiatry.

Presynaptic impairment of cerebellar inhibitory synapses by an autoantibody to glutamate decarboxylase

H. Mitoma, Takayoshi Kobayashi, Si-young Song, 2000, Journal of the Neurological Sciences.

NUCLEAR BRIDGES IN MULTINUCLEATED GIANT CELLS ASSOCIATED WITH PRIMARY LYMPHOMA OF THE BRAIN IN AN AIDS PATIENT.: 50

H. Mizusawa, A. Hirano, J. Llena, 1987 .

Competition between 11C-raclopride and endogenous dopamine in Parkinson's disease

K. Ishii, K. Oda, K. Ishiwata, 2010, Nuclear medicine communications.

ONLINE REGISTRY FOR THE PREVENTION OF DEMENTIA IN JAPAN

H. Matsuda, E. Imabayashi, H. Shimada, 2016, Alzheimer's & Dementia.