M. Nishizawa

T. Nakada, A. Kakita, Hitoshi Takahashi, 2011, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

Tract‐by‐Tract Morphometric and Diffusivity Analyses In Vivo of Spinocerebellar Degeneration

T. Nakada, H. Matsuzawa, K. Akazawa, 2009, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

Clinical and genetic characterizations of 16q‐linked autosomal dominant spinocerebellar ataxia (AD‐SCA) and frequency analysis of AD‐SCA in the Japanese population

M. Nishizawa, T. Ikeuchi, O. Onodera, 2007, Movement disorders : official journal of the Movement Disorder Society.

Effect of rovatirelin in patients with cerebellar ataxia: two randomised double-blind placebo-controlled phase 3 trials

M. Nishizawa, O. Onodera, A. Hirakawa, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Effects of Angiopoietin-1 on Hemorrhagic Transformation and Cerebral Edema after Tissue Plasminogen Activator Treatment for Ischemic Stroke in Rats

T. Nakada, T. Shimohata, M. Nishizawa, 2014, PloS one.

Enhanced Accumulation of Phosphorylated α-Synuclein and Elevated β-Amyloid 42/40 Ratio Caused by Expression of the Presenilin-1 ΔT440 Mutant Associated with Familial Lewy Body Disease and Variant Alzheimer's Disease

A. Kakita, T. Iwatsubo, A. Miyashita, 2007, The Journal of Neuroscience.

Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia

R. Kuwano, M. Nishizawa, T. Ikeuchi, 2007, Journal of Medical Genetics.

Mitochondrial angiopathy in cerebral blood vessels of mitochondrial eneephalomyopathy

T. Miyatake, S. Ohara, M. Nishizawa, 2004, Acta Neuropathologica.

Therapeutic strategies to attenuate hemorrhagic transformation after tissue plasminogen activator treatment for acute ischemic stroke

T. Shimohata, M. Nishizawa, M. Kanazawa, 2013 .

Frontotemporal dementia with co-occurrence of astrocytic plaques and tufted astrocytes, and severe degeneration of the cerebral white matter: a variant of corticobasal degeneration?

A. Kakita, Hitoshi Takahashi, Y. Piao, 2005, Acta Neuropathologica.

Cardiac sympathetic denervation in Parkinson’s disease linked to SNCA duplication

A. Kakita, Hitoshi Takahashi, T. Uchihara, 2008, Acta Neuropathologica.

Ischemic tolerance: mechanism of neuroprotective effect and clinical applications

T. Shimohata, M. Nishizawa, Tetsuya Takahashi, 2015 .

Atypical Parkinsonism in distal myopathy with rimmed vacuoles

M. Nishizawa, T. Ozawa, Keiko Tanaka, 2008, Movement disorders : official journal of the Movement Disorder Society.

Multiple therapeutic effects of a growth factor, progranulin on ischemic brain injury

T. Shimohata, M. Nishizawa, M. Koyama, 2016 .

Treatment against hemorrhagic transformation after delayed tPA treatment that targets vascular remodeling factors

T. Shimohata, M. Nishizawa, M. Kanazawa, 2015 .

Translational research that enables inhibition of hemorrhagic transformation after tissue plasminogen activator treatment for ischemic stroke

T. Shimohata, M. Nishizawa, M. Kanazawa, 2015 .

A patient with right internal carotid artery territory infarctionduring intravenous recombinant tissue plasminogen activator treatment for left middle cerebral artery territory ischemic stroke

T. Shimohata, M. Nishizawa, Y. Akaiwa, 2012 .

[Clinical and pathological spectrum of TDP-43 associated ALS].

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2010, Rinsho shinkeigaku = Clinical neurology.

Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions

A. Kakita, Hitoshi Takahashi, M. Yamada, 2008, Acta Neuropathologica.

Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology

A. Kakita, Hitoshi Takahashi, M. Yamada, 2008, Acta Neuropathologica.

Submucosal mast cells in the gastrointestinal tract are a target of staphylococcal enterotoxin type A.

K. Omoe, A. Nakane, M. Nishizawa, 2012, FEMS immunology and medical microbiology.

A mutation in the immunoproteasome subunit PSMB8 causes autoinflammation and lipodystrophy in humans.

D. Standley, Keiji Tanaka, Hitoshi Takahashi, 2011, The Journal of clinical investigation.

A case of slowly progressive anti-Yo-associated paraneoplastic cerebellar degeneration successfully treated with antitumor and immunotherapy.

M. Nishizawa, I. Kawachi, Y. Higuchi, 2016, Rinsho shinkeigaku = Clinical neurology.

SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians

J. Haines, M. Pericak-Vance, G. Schellenberg, 2013, PloS one.

[Gray matter lesions and cognitive impairment in multiple sclerosis].

M. Nishizawa, I. Kawachi, E. Saji, 2014, Rinsho shinkeigaku = Clinical neurology.

Chorea as the First Sign in a Patient with Elderly-Onset Systemic Lupus Erythematosus

M. Nishizawa, I. Kawachi, T. Ozawa, 2012, Case reports in neurological medicine.

Depletion of medullary serotonergic neurons in patients with multiple system atrophy who succumbed to sudden death

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2009, Brain : a journal of neurology.

High frequency of calcification in basal ganglia on brain computed tomography images in Japanese older adults

M. Kanematsu, H. Hoshi, T. Asano, 2013, Geriatrics & gerontology international.

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

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

Early diagnosis of hepatic intravascular lymphoma: a case report and literature review.

Yoshifumi Takahashi, M. Takeuchi, H. Sone, 2014, Internal medicine.

Dissociation between intact vibratory sensation and impaired joint position sensation may predict ataxia of spinal origin

M. Nishizawa, N. Endo, O. Onodera, 2016 .

Features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.

M. Nishizawa, O. Onodera, H. Nozaki, 2014, Stroke.

A Fulminant Case of Granulomatosis with Polyangiitis with Meningeal and Parenchymal Involvement

Hitoshi Takahashi, I. Narita, M. Yamada, 2015, Case Reports in Neurology.

A case report of five rheumatoid patients with posterior atlanto-axial subluxation

M. Nishizawa, 一井上, 良樹横山, 1987 .

Familial amyotrophic lateral sclerosis: a SOD1-unrelated Japanese family of bulbar type with Bunina bodies and ubiquitin-positive skein-like inclusions in lower motor neurons

Hitoshi Takahashi, M. Nishizawa, O. Onodera, 2007, Acta Neuropathologica.

Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese

M. Nishizawa, Y. Takiyama, K. Tashiro, 2001, Journal of medical genetics.

Primary lateral sclerosis: Upper‐motor‐predominant amyotrophic lateral sclerosis with frontotemporal lobar degeneration – immunohistochemical and biochemical analyses of TDP‐43

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.

Sporadic four-repeat tauopathy with frontotemporal degeneration, parkinsonism and motor neuron disease

A. Kakita, A. Lees, T. Révész, 2005, Acta Neuropathologica.

Variants associated with Gaucher disease in multiple system atrophy

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

Multiplex families with multiple system atrophy.

I. Kanazawa, S. Tsuji, A. Kakita, 2007, Archives of neurology.

[Reliability of the Japanese version of the Scale for the Assessment and Rating of Ataxia (SARA)].

G. Sobue, K. Nakashima, T. Shimohata, 2009, Brain and nerve = Shinkei kenkyu no shinpo.

Immune‐mediated hypertrophic pachymeningitis: Clinical significance of anti‐neutrophil cytoplasmic antibody and granulomatosis with polyangiitis (Wegener's granulomatosis)

M. Nishizawa, I. Kawachi, A. Yokoseki, 2014 .

[Clinical features of poor-prognosis patients with adult bacterial meningitis].

T. Shimohata, M. Nishizawa, Keiko Tanaka, 2010, Rinsho shinkeigaku = Clinical neurology.

Early development of autonomic dysfunction may predict poor prognosis in patients with multiple system atrophy.

A. Kakita, Hitoshi Takahashi, Y. Piao, 2007, Archives of neurology.

Predictors of cognitive impairment in multiple system atrophy

T. Shimohata, M. Nishizawa, O. Onodera, 2017, Journal of the Neurological Sciences.

Mechanisms and prevention of sudden death in multiple system atrophy.

T. Shimohata, H. Taniguchi, M. Inoue, 2016, Parkinsonism & related disorders.

Laryngeal stridor in multiple system atrophy: Clinicopathological features and causal hypotheses

N. Aizawa, M. Nishizawa, T. Ozawa, 2016, Journal of the Neurological Sciences.

Maintaining glottic opening in multiple system atrophy: Efficacy of serotonergic therapy

T. Shimohata, N. Aizawa, M. Nishizawa, 2012, Movement disorders : official journal of the Movement Disorder Society.

Nutritional Status and Changes in Body Weight in Patients with Multiple System Atrophy

T. Shimohata, M. Nishizawa, M. Shiobara, 2016, European Neurology.

Esophageal Involvement in Multiple System Atrophy

T. Shimohata, K. Hori, H. Taniguchi, 2015, Dysphagia.

Discontinuation of continuous positive airway pressure treatment in multiple system atrophy.

T. Shimohata, N. Aizawa, M. Nishizawa, 2014, Sleep medicine.

The circulating level of leptin and blood pressure in patients with multiple system atrophy

H. Sone, M. Nishizawa, A. Ishikawa, 2014, Journal of the Neurological Sciences.

Early clinical features of patients with progressive supranuclear palsy with predominant cerebellar ataxia.

Hitoshi Takahashi, T. Shimohata, M. Nishizawa, 2013, Parkinsonism & related disorders.

Tremulous arytenoid movements predict severity of glottic stenosis in multiple system atrophy

T. Shimohata, M. Nishizawa, M. Tomita, 2010, Movement Disorders.

Reduced bowel sounds in Parkinson’s disease and multiple system atrophy patients

M. Nishizawa, O. Onodera, T. Ozawa, 2011, Clinical Autonomic Research.

[Clinical features of multiple system atrophy].

T. Shimohata, M. Nishizawa, 2009, Rinsho shinkeigaku = Clinical neurology.

Multiple System Atrophy with Progressive Nocturnal Hypoxemia: Case Report with Polysomnography and Continuous Positive Airway Pressure Treatment

T. Shimohata, M. Nishizawa, H. Nakayama, 2006, European Neurology.

Depression and psychiatric symptoms preceding onset of dementia in a family with early-onset Alzheimer disease with a novel PSEN1 mutation

A. Miyashita, R. Kuwano, M. Nishizawa, 2009, Journal of Neurology.

Mutational Analysis in Early-Onset Familial Dementia in the Japanese Population

A. Miyashita, R. Kuwano, T. Imamura, 2008, Dementia and Geriatric Cognitive Disorders.

Enhanced accumulation of phosphorylated alpha-synuclein and elevated beta-amyloid 42/40 ratio caused by expression of the presenilin-1 deltaT440 mutant associated with familial Lewy body disease and variant Alzheimer's disease.

A. Kakita, T. Iwatsubo, A. Miyashita, 2007, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[Diagnoses of corticobasal syndrome and corticobasal degeneration].

T. Shimohata, M. Nishizawa, I. Aiba, 2016, Rinsho shinkeigaku = Clinical neurology.

Interleukin 3 as a trophic factor for central cholinergic neurons in vitro and in vivo

T. Tabira, M. Nishizawa, T. Kunishita, 1990, Neuron.

Polyglutamine represses cAMP-responsive-element-mediated transcription without aggregate formation

S. Tsuji, M. Nishizawa, O. Onodera, 2005, Neuroreport.

Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene

A. Kakita, Hitoshi Takahashi, T. Shimohata, 2013, Acta Neuropathologica.

Behavioral recovery in 6-hydroxydopamine-lesioned rats by cotransduction of striatum with tyrosine hydroxylase and aromatic L-amino acid decarboxylase genes using two separate adeno-associated virus vectors.

K. Ozawa, M. Urabe, H. Ichinose, 1998, Human gene therapy.

Pathology and sensitivity of current clinical criteria in corticobasal syndrome

Hitoshi Takahashi, T. Shimohata, I. Tomita, 2014, Movement disorders : official journal of the Movement Disorder Society.

[Clinical aspects of corticobasal syndrome].

T. Shimohata, M. Nishizawa, 2013, Brain and nerve = Shinkei kenkyu no shinpo.

TDP‐43 mutation in familial amyotrophic lateral sclerosis

A. Kakita, Hitoshi Takahashi, K. Okamoto, 2008, Annals of neurology.

Identification of GFAP gene mutation in hereditary adult‐onset Alexander's disease

H. Shimazaki, Y. Matsubara, Y. Aoki, 2002, Annals of neurology.

Prevention of dopaminergic neuron death by adeno-associated virus vector-mediated GDNF gene transfer in rat mesencephalic cells in vitro

K. Ozawa, K. Kiuchi, M. Urabe, 1998, Neuroscience Letters.

A serial MRI study in a patient with progressive supranuclear palsy with cerebellar ataxia.

Hitoshi Takahashi, T. Shimohata, M. Nishizawa, 2012, Parkinsonism & related disorders.

Botulinum toxin A injections improve apraxia of eyelid opening without overt blepharospasm associated with neurodegenerative diseases

T. Shimohata, M. Nishizawa, O. Onodera, 2008, Movement disorders : official journal of the Movement Disorder Society.

Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity

A. Kakita, A. Miyashita, Hitoshi Takahashi, 2010, Acta Neuropathologica.

Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-β1 via cleavage of proTGF-β1.

K. Arima, Hitoshi Takahashi, M. Nishizawa, 2011, Human molecular genetics.

Lymphokine production by encephalitogenic and non-encephalitogenic T-cell clones reactive to the same antigenic determinant

T. Tabira, K. Nagashima, M. Nishizawa, 1990, Journal of Neuroimmunology.

Audiologic Findings in Patients with a Point Mutation at Nucleotide 3,243 of Mitochondrial Dna

M. Nishizawa, T. Ishida, Y. Tamagawa, 1997, The Annals of otology, rhinology, and laryngology.

Quantitative determination of 6-keto prostaglandin F1 alpha in biological fluids by capillary gas chromatography-chemical ionization mass spectrometry.

I. Morita, S. Murota, M. Nishizawa, 1980, Journal of chromatography.

A case of McLeod syndrome with unusually severe myopathy

I. Nonaka, M. Reid, M. Nishizawa, 1999, Journal of the Neurological Sciences.

ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.

Robert H. Brown, A. Fujiyama, A. Toyoda, 2013, American journal of human genetics.

[A case of amyotrophic lateral sclerosis/frontotemporal lobar degeneration with apraxia of eyelid opening].

M. Nishizawa, T. Ikeuchi, K. Kasuga, 2010, Rinsho shinkeigaku = Clinical neurology.

[Patient with limbic encephalitis associated with anti-voltage-gated potassium channel antibodies who presented with insomnia and hand tremor].

T. Shimohata, M. Nishizawa, I. Kawachi, 2008, Rinsho shinkeigaku = Clinical neurology.

Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology

A. Kakita, Hitoshi Takahashi, T. Someya, 2016, Brain pathology.

Increased Levels of Soluble LR11 in Cerebrospinal Fluid of Patients with Alzheimer Disease

A. Kakita, Hitoshi Takahashi, Hiroyuki Ebinuma, 2010, Dementia and Geriatric Cognitive Disorders.

Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease

N. Matsumoto, A. Miyashita, R. Kuwano, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

Transportin 1 accumulates in FUS inclusions in adult‐onset ALS without FUS mutation

A. Kakita, H. Takahashi, M. Nishizawa, 2013, Neuropathology and applied neurobiology.

Multiple therapeutic effects of progranulin on experimental acute ischaemic stroke.

T. Nakada, M. Nishihara, T. Shimohata, 2015, Brain : a journal of neurology.

TRPM7 is not associated with amyotrophic lateral sclerosis‐parkinsonism dementia complex in the Kii peninsula of Japan

S. Tsuji, A. Miyashita, R. Kuwano, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Anti‐aquaporin‐4 antibody‐positive optic neuritis

M. Takagi, H. Abe, M. Nishizawa, 2009, Acta ophthalmologica.

Abnormal ghrelin secretion contributes to gastrointestinal symptoms in multiple system atrophy patients

T. Kondo, M. Nishizawa, A. Ishikawa, 2013, Autonomic Neuroscience.

Regulatory T cells in paraneoplastic neurological syndromes

M. Nishizawa, Keiko Tanaka, K. Tanaka, 2008, Journal of Neuroimmunology.

Frequency of nocturnal sudden death in patients with multiple system atrophy

T. Shimohata, M. Nishizawa, M. Tomita, 2008, Journal of Neurology.

Visualization of the Intimal Flap in Intracranial Arterial Dissection Using High‐Resolution 3T MRI

T. Nakada, Masaki Watanabe, M. Nishizawa, 2017, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

Machado-Joseph disease: Cerebellar ataxia and autonomic dysfunction in a patient with the shortest known expanded allele (56 CAG repeat units) of the MJD1 gene

M. Nishizawa, Y. Takiyama, K. Sakoe, 1997, Neurology.

Cerebellar Ataxia Rehabilitation Trial in Degenerative Cerebellar Diseases

Noriaki Hattori, Ichiro Miyai, Masahito Mihara, 2012, Neurorehabilitation and neural repair.

Neuroblastoma ampliﬁed sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger e Hue¨t anomaly

A. Miyashita, Hitoshi Takahashi, Svetlana Potapova, 2022 .

Long‐term disability and prognosis in dentatorubral‐pallidoluysian atrophy: A correlation with CAG repeat length

M. Nishizawa, T. Ikeuchi, O. Onodera, 2010, Movement disorders : official journal of the Movement Disorder Society.

Total deletion and a missense mutation of ITPR1 in Japanese SCA15 families

S. Tsuji, M. Nishizawa, Yuji Takahashi, 2008, Neurology.

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.

Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia.

S. Tsuji, M. Yamada, M. Nishizawa, 2011, Brain : a journal of neurology.

Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3′-phosphate and 3′-phosphoglycolate ends

S. Tsuji, M. Nishizawa, H. Date, 2007, Nucleic acids research.

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: The aprataxin gene mutations

S. Tsuji, H. Shimazaki, M. Nishizawa, 2002, Neurology.

Importance of the Q/N-rich segment for protein stability of endogenous mouse TDP-43

M. Yokoyama, M. Nishizawa, T. Sasaoka, 2022, Scientific Reports.

Importance of the Q/N-rich Segment for Protein Stability and Activity of Endogenous Mouse TDP-43

M. Yokoyama, M. Nishizawa, T. Sasaoka, 2021 .

Biochemical and histopathological alterations in TAR DNA‐binding protein‐43 after acute ischemic stroke in rats

T. Nakada, A. Kakita, Hitoshi Takahashi, 2011, Journal of neurochemistry.

Japanese POEMS syndrome with Thalidomide (J-POST) Trial: study protocol for a phase II/III multicentre, randomised, double-blind, placebo-controlled trial

G. Sobue, T. Kanda, J. Kira, 2015, BMJ Open.

C9ORF72 repeat‐associated non‐ATG‐translated polypeptides are distributed independently of TDP‐43 in a Japanese patient with c9ALS

A. Kakita, M. Hasegawa, Hitoshi Takahashi, 2014, Neuropathology and applied neurobiology.

Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72

Hitoshi Takahashi, M. Nishizawa, S. Kuwabara, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

A clinical and radiological study of cervical spinal lesions in patients with progressive rheumatoid arthritis

M. Nishizawa, 1993 .

[FTLD/ALS as TDP-43 proteinopathies].

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2010, Rinsho shinkeigaku = Clinical neurology.

A Japanese SPG4 family with a novel missense mutation of the SPG4 gene: intrafamilial variability in age at onset and clinical severity

H. Shimazaki, M. Nishizawa, Y. Takiyama, 2002, Acta neurologica Scandinavica.

A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic study

H. Shimazaki, M. Nishizawa, Y. Takiyama, 2001, Journal of the Neurological Sciences.

Accumulation of glycosphingolipids in spinal and sympathetic ganglia of a symptomatic heterozygote of Fabry's disease

T. Miyatake, I. Hozumi, M. Nishizawa, 1989, Journal of the Neurological Sciences.

Single sperm analysis of the CAG repeats in the gene for Machado-Joseph disease (MJD1): evidence for non-Mendelian transmission of the MJD1 gene and for the effect of the intragenic CGG/GGG polymorphism on the intergenerational instability.

S. Tsuji, M. Nishizawa, Y. Takiyama, 1997, Human molecular genetics.

Fibromyalgia in a Patient with Cushing's Disease Accompanied by Central Hypothyroidism

A. Kakita, H. Sone, Takaho Yamada, 2016, Internal medicine.

Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation

Z. Wszolek, T. Kawarai, Kunihiro Yoshida, 2016, European journal of neurology.

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia

Z. Wszolek, B. Woodruff, M. Nishizawa, 2014 .

A patient with anti-aquaporin 4 antibody who presented with recurrent hypersomnia, reduced orexin (hypocretin) level, and symmetrical hypothalamic lesions.

T. Shimohata, M. Nishizawa, O. Onodera, 2009, Sleep medicine.

Methylmercury Causes Blood-Brain Barrier Damage in Rats via Upregulation of Vascular Endothelial Growth Factor Expression

T. Shimohata, M. Nishizawa, M. Koyama, 2017, PloS one.

Long-term therapeutic efficacy and safety of low-dose tacrolimus (FK506) for myasthenia gravis

S. Tsuji, T. Shimohata, M. Nishizawa, 2006, Journal of the Neurological Sciences.

Nonfunctional intra‐ and suprasellar tumor in a patient with visual disturbance and panhypopituitarism

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2016, Neuropathology : official journal of the Japanese Society of Neuropathology.

Effects of Alda-1, an Aldehyde Dehydrogenase-2 Agonist, on Hypoglycemic Neuronal Death

T. Nakada, M. Tsujita, T. Shimohata, 2015, PloS one.

Characteristic microglial features in patients with hereditary diffuse leukoencephalopathy with spheroids

A. Kakita, Hitoshi Takahashi, H. Takebayashi, 2016, Annals of neurology.

Alterations of oligodendrocytes and demyelination in the spinal cord of patients with mitochondrial encephalomyopathy

T. Miyatake, S. Ohara, Hitoshi Takahashi, 1988, Journal of the Neurological Sciences.

Shared carbohydrate antigenic determinant between the myelin-associated glycoprotein (MAG) and lung cancers An immunohistochemical study by an anti-MAG IgM monoclonal antibody

T. Miyatake, T. Inuzuka, I. Hozumi, 1987, Journal of Neuroimmunology.

Human natural killer cell activity is reduced by treatment of anti-myelin-associated glycoprotein (MAG) monoclonal mouse IgM antibody and complement

T. Miyatake, T. Inuzuka, M. Nishizawa, 1985, Journal of Neuroimmunology.

Autoproliferative and self-reactive T-cell lines from patients with HTLV-I-associated myelopathy.

T. Tabira, M. Nishizawa, M. Osame, 1990, The Tohoku journal of experimental medicine.

Induction and regulation of IL-8 and MCAF production in human brain tumor cell lines and brain tumor tissues.

K. Matsushima, N. Mukaida, M. Nishizawa, 1993, European cytokine network.

Cytotoxic and suppressor activities in patients with HTLV-I-associated myelopathy

T. Tabira, M. Nishizawa, M. Osame, 1991, Journal of Neuroimmunology.

Association of a particular amino acid sequence of the HLA‐DR β1 chain with HTLV‐I‐associated myelopathy

T. Tabira, K. Tokunaga, M. Nishizawa, 1990, European journal of immunology.

Developmental and aging changes in the expression patterns of beta-amyloid in the brains of normal and down syndrome cases

T. Tabira, S. Takashima, T. Mito, 1990, Brain and Development.

Susceptibility to proteolipid apoprotein and its encephalitogenic determinants in mice.

T. Tabira, M. Nishizawa, T. Kunishita, 1990, International archives of allergy and applied immunology.

Cervical dystonia associated with spinocerebellar ataxia type 2 successfully treated with levodopa: A case report

T. Shimohata, M. Nishizawa, J. Tokunaga, 2009, Movement disorders : official journal of the Movement Disorder Society.

Japanese case of Emery–Dreifuss muscular dystrophy with a novel LMNA missense mutation

I. Nishino, M. Nishizawa, S. Mitsuhashi, 2016 .

Sensorineural hearing impairment non-syndromic, dominant DFNA11.

K. Steel, M. Nishizawa, T. Ishida, 2000, Advances in oto-rhino-laryngology.

Production and Characterization of Monoclonal Antibodies Against Myelin‐Associated Glycoprotein

T. Miyatake, S. Sato, T. Inuzuka, 1986, Journal of neurochemistry.

Characterization of the antigen determinant on HSB-2 cells shared with myelin-associated glycoprotein (MAG) using monoclonal antibodies

T. Miyatake, T. Inuzuka, M. Nishizawa, 1986, Journal of Neuroimmunology.

Human placental sialidase: further purification and characterization.

T. Miyatake, M. Nishizawa, M. Hiraiwa, 1988, Journal of biochemistry.

Human placental sialidase: partial purification and characterization.

T. Miyatake, M. Nishizawa, M. Hiraiwa, 1987, Journal of biochemistry.

M. Nishizawa, O. Onodera, K. Hara, 2007, Movement Disorders.

Spontaneous Middle Cerebral Artery Dissection Demonstrated by High-Resolution T1-Weighted 3D Image

T. Nakada, T. Shimohata, M. Nishizawa, 2013, Cerebrovascular Diseases.

Progressive myoclonus epilepsy: extraneuronal brown pigment deposition and system neurodegeneration in the brains of Japanese patients with novel SCARB2 mutations

A. Kakita, Hitoshi Takahashi, S. Takeda, 2014, Neuropathology and applied neurobiology.

A mitochondrial encephalomyopathy with cardiomyopathy A case revealing a defect of complex I in the respiratory chain

T. Miyatake, M. Nishizawa, E. Ohama, 1987, Journal of the Neurological Sciences.

Clinical and neuroimaging features of patient with early-onset Parkinson's disease with dementia carrying SNCA p.G51D mutation.

A. Miyashita, R. Kuwano, M. Nishizawa, 2014, Parkinsonism & related disorders.

Factors influencing the cognitive function in patients with multiple system atrophy

T. Shimohata, M. Nishizawa, M. Tomita, 2010, Movement disorders : official journal of the Movement Disorder Society.

A Patient with Fragile X-Associated Tremor/Ataxia Syndrome Presenting with Executive Cognitive Deficits and Cerebral White Matter Lesions

M. Nishizawa, T. Ikeuchi, K. Kasuga, 2011, Case Reports in Neurology.

Safety of unsedated PEG placement using transoral ultrathin endoscopy in patients with amyotrophic lateral sclerosis

M. Takeuchi, M. Nishizawa, K. Mizuno, 2016, Nutritional neuroscience.

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.

Anti-aquaporin 4 antibody in selected Japanese multiple sclerosis patients with long spinal cord lesions

K. Tanaka, T. Nakada, M. Tsujita, 2007, Multiple sclerosis.

Serial Assessments of Delayed Encephalopathy after Carbon Monoxide Poisoning Using Magnetic Resonance Spectroscopy and Diffusion Tensor Imaging on 3.0T System

T. Nakada, H. Matsuzawa, M. Nishizawa, 2007, European Neurology.

Cryptococcal meningitis successfully treated with voriconazole and low‐dose amphotericin B

T. Shimohata, M. Nishizawa, T. Ozawa, 2014 .

Safety and efficacy of thalidomide in patients with POEMS syndrome: a multicentre, randomised, double-blind, placebo-controlled trial

G. Sobue, T. Kanda, J. Kira, 2016, The Lancet Neurology.

Therapeutic Strategies to Attenuate Hemorrhagic Transformation After Tissue Plasminogen Activator Treatment for Acute Ischemic Stroke

T. Shimohata, M. Nishizawa, M. Kanazawa, 2013, Journal of atherosclerosis and thrombosis.

Molecular cloning of a full-length cDNA for human alpha-N-acetylgalactosaminidase (alpha-galactosidase B).

K. Sakimura, T. Miyatake, T. Isobe, 1989, Biochemical and Biophysical Research Communications - BBRC.

New mutation in the non‐gigantic exon of SACS in Japanese siblings

T. Shimohata, M. Nishizawa, O. Onodera, 2007, Movement disorders : official journal of the Movement Disorder Society.

Selective silencing of a mutant transthyretin allele by small interfering RNAs.

M. Nishizawa, O. Onodera, S. Igarashi, 2005, Biochemical and biophysical research communications.

Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.

S. Tsuji, K. Arima, Tadashi Yamamoto, 2009, The New England journal of medicine.

Cerebellar involvement in progressive supranuclear palsy: A clinicopathological study

A. Kakita, Hitoshi Takahashi, T. Shimohata, 2009, Movement disorders : official journal of the Movement Disorder Society.

A Japanese family with idiopathic basal ganglia calcification with novel SLC20A2 mutation presenting with late-onset hallucination and delusion

M. Nishizawa, T. Ikeuchi, T. Konno, 2014, Journal of Neurology.

Characteristics of Aquaporin Expression Surrounding Senile Plaques and Cerebral Amyloid Angiopathy in Alzheimer Disease

A. Kakita, Hitoshi Takahashi, Y. Ugawa, 2012, Journal of neuropathology and experimental neurology.

Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger–Huët anomaly

Osamu Onodera, Masatoyo Nishizawa, Akinori Miyashita, 2010, Journal of Medical Genetics.

New HSN2 mutation in Japanese patient with hereditary sensory and autonomic neuropathy type 2

M. Nishizawa, O. Onodera, K. Hara, 2006, Neurology.

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.

F. Pasquier, A. Durr, D. Hannequin, 2008, Brain : a journal of neurology.

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

S. Sugano, S. Tsuji, T. Yuasa, 2001, Nature Genetics.

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT

S. Tsuji, Hitoshi Takahashi, H. Takahashi, 1996, Nature Genetics.

Microglia preconditioned by oxygen-glucose deprivation promote functional recovery in ischemic rats

T. Shimohata, M. Nishizawa, O. Onodera, 2017, Scientific Reports.

Conformational Disease and RNA Disease Theory in the Context of Neurodegenerative Diseases

M. Nishizawa, O. Onodera, Tomohiko Ishihara, 2015 .

A mutant PSEN1 causes dementia with lewy bodies and variant Alzheimer's disease

A. Miyashita, Hitoshi Takahashi, R. Kuwano, 2005, Annals of neurology.

TDP-43 transports ribosomal protein mRNA to regulate axonal local translation in neuronal axons

Rehab F. Abdelhamid, K. Sakimura, T. Araki, 2020, Acta Neuropathologica.

Minor splicing pathway is not minor any more: Implications for the pathogenesis of motor neuron diseases

M. Nishizawa, A. Shiga, O. Onodera, 2014, Neuropathology : official journal of the Japanese Society of Neuropathology.

Decreased number of Gemini of coiled bodies and U12 snRNA level in amyotrophic lateral sclerosis.

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2013, Human molecular genetics.

Patient with insidious hypoactive delirium associated with pregabalin

T. Shimohata, M. Nishizawa, O. Onodera, 2013 .

SYNE1-ataxia: clinicopathologic features of an autopsied patient with novel compound heterozygous mutations.

A. Kakita, A. Miyashita, M. Nishizawa, 2022, Journal of neuropathology and experimental neurology.

Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL

R. Kuwano, M. Nishizawa, Mari Yoshida, 2016, Neurology.

Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes

T. Matsukawa, S. Tsuji, N. Shimozawa, 2010, neurogenetics.

The gene for Machado–Joseph disease maps to human chromosome 14q

Y. Kagawa, O. Onodera, I. Kanazawa, 1993, Nature Genetics.

α-Synuclein as CSF and Blood Biomarker of Dementia with Lewy Bodies

M. Nishizawa, T. Ikeuchi, K. Kasuga, 2012, International journal of Alzheimer's disease.

[A mitochondrial encephalomyopathy: a case of a defect of complex I in the electron transport chain].

M. Nishizawa, E. Ohama, T. Atsumi, 1987, Rinsho shinkeigaku = Clinical neurology.

[Toxocara canis myelitis].

M. Nishizawa, T. Ozawa, Keiko Tanaka, 2007, Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine.

Hypertrophic pachymeningitis: significance of myeloperoxidase anti-neutrophil cytoplasmic antibody.

A. Kakita, K. Akazawa, Hitoshi Takahashi, 2014, Brain : a journal of neurology.

The Clinical Features, Risk Factors, and Surgical Treatment of Cervicogenic Headache in Patients With Cervical Spine Disorders Requiring Surgery

T. Shimohata, M. Nishizawa, O. Onodera, 2017, Headache.

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

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

[An autopsy case of systemic vasculitis associated with hepatitis C virus-related mixed cryoglobulinemia presenting severe peripheral neuropathy].

S. Tsuji, A. Kakita, Hitoshi Takahashi, 2004, Rinsho shinkeigaku = Clinical neurology.

Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS)

Hiroshi Suzuki, T. Miyatake, S. Horai, 1989, Journal of the Neurological Sciences.

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

Steve D. M. Brown, K. Steel, X. Liu, 1997, Nature Genetics.

Roles of inositol 1,4,5-trisphosphate receptors in spinocerebellar ataxias

M. Nishizawa, O. Onodera, M. Tada, 2016, Neurochemistry International.

Biochemical and clinical analysis of accumulated glycolipids in symptomatic heterozygotes of angiokeratoma corporis diffusum (Fabry's disease) in comparison with hemizygotes.

T. Miyatake, I. Hozumi, M. Nishizawa, 1990, Journal of lipid research.

Sporadic ataxias in Japan – a population-based epidemiological study

Osamu Onodera, Masatoyo Nishizawa, S. Tsuji, 2008, The Cerebellum.

Functional characterization of the P1059L mutation in the inositol 1,4,5-trisphosphate receptor type 1 identified in a Japanese SCA15 family.

K. Mikoshiba, T. Michikawa, M. Nishizawa, 2011, Biochemical and biophysical research communications.

Clinical features of neuromyelitis optica in a large Japanese cohort: comparison between phenotypes

Masatoyo Nishizawa, Kenji Sakimura, Makoto Matsui, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy.

T. Miyatake, T. Ozawa, M. Nishikimi, 1986, Biochemical and biophysical research communications.

Floppy epiglottis as a contraindication of CPAP in patients with multiple system atrophy

T. Shimohata, N. Aizawa, M. Nishizawa, 2011, Neurology.

Letters to the Editor Related to New Topics Catatonia during Deep Brain Stimulator Implantation Complicated by Intracranial Hemorrhage

T. Shimohata, M. Nishizawa, M. Tomita, 2010 .

Daytime hypoxemia, sleep-disordered breathing, and laryngopharyngeal findings in multiple system atrophy.

Tetsutaro Ozawa, Osamu Onodera, Kenshi Terajima, 2007, Archives of neurology.

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2007, Acta Neuropathologica.

Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat.

J. Weissenbach, Y. Agid, R. Sherrington, 1996, Human molecular genetics.

[A late-onset case of oculopharyngeal muscular dystrophy carrying a (GCG)8 repeat expansion in the PAPBN1 gene].

M. Nishizawa, T. Ikeuchi, O. Onodera, 2005, Rinsho shinkeigaku = Clinical neurology.

Assessment of Ataxia Rating Scales and Cerebellar Functional Tests: Critique and Recommendations

G. Stebbins, A. Durr, P. Martínez-Martín, 2020, Movement disorders : official journal of the Movement Disorder Society.

Hyperphosphorylation of Tau Induced by Naturally Secreted Amyloid-β at Nanomolar Concentrations Is Modulated by Insulin-dependent Akt-GSK3β Signaling Pathway*

M. Nishizawa, T. Ikeuchi, K. Kasuga, 2012, The Journal of Biological Chemistry.

Dropped head syndrome in amyotrophic lateral sclerosis

Hitoshi Takahashi, T. Shimohata, M. Nishizawa, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

An unusual case of facial diplegia

S. Kusunoki, M. Nishizawa, Y. Takiyama, 1999, Muscle & nerve.

Symptomatic narcolepsy in patients with neuromyelitis optica and multiple sclerosis: new neurochemical and immunological implications.

T. Shimohata, S. Nishino, M. Nishizawa, 2009, Archives of neurology.

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.

H. Zoghbi, S. Tsuji, A. Durr, 1998, American journal of human genetics.

Single sperm analysis of the CAG repeats in the gene for dentatorubral-pallidoluysian atrophy (DRPLA): the instability of the CAG repeats in the DRPLA gene is prominent among the CAG repeat diseases.

M. Nishizawa, Y. Takiyama, K. Sakoe, 1999, Human molecular genetics.

Characteristics and exacerbating factors of chronic low back pain in Parkinson’s disease

T. Shimohata, M. Nishizawa, N. Endo, 2015, International Orthopaedics.

Mitochondrial DNA mutation at nucleotide 1555 in a patient with bilateral sensorineural hearing loss of unknown etiology.

K. Abe, M. Nishizawa, T. Ishida, 1996, Acta oto-laryngologica.

Pathologic and immunologic profiles of a limited form of neuromyelitis optica with myelitis

M. Tsujita, A. Kakita, K. Sakimura, 2009, Neurology.

Creutzfeldt‐Jakob disease with an M232R substitution: report of a patient showing slowly progressive disease with abundant plaque‐like PrP deposits in the cerebellum

Hitoshi Takahashi, M. Yamada, M. Nishizawa, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

クロイツフェルト・ヤコプ病における病名告知，治療の検討

T. Shimohata, M. Nishizawa, M. Tada, 2014 .

Partial deletions of putative adrenoleukodystrophy (ALD) gene in Japanese ALD patients

S. Tsuji, J. Mosser, T. Miyatake, 1995 .

Successful twin pregnancy in a patient with parkin-associated autosomal recessive juvenile parkinsonism

K. Haino, Kenichi Tanaka, T. Shimohata, 2011, BMC neurology.

Apparent diffusion coefficient reduction might be a predictor of poor outcome in patients with posterior reversible encephalopathy syndrome

T. Shimohata, M. Nishizawa, K. Okamoto, 2017, Journal of the Neurological Sciences.

A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2‐cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4‐qter

S. Tsuji, M. Nishizawa, Y. Takiyama, 2000, Annals of neurology.

Reduction rate of body mass index predicts prognosis for survival in amyotrophic lateral sclerosis: A multicenter study in Japan

Y. Kuroiwa, Toshio Shimizu, T. Komori, 2012, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

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.

Chronic myositis with cardiomyopathy and respiratory failure associated with mild form of organ-specific autoimmune diseases

M. Nishizawa, M. Tada, M. Kanazawa, 2007, Clinical Rheumatology.

Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription

I. Kanazawa, S. Tsuji, Hitoshi Takahashi, 2000, Nature Genetics.

IP3 Receptors in Neurodegenerative Disorders: Spinocerebellar Ataxias and Huntington’s and Alzheimer’s Diseases

M. Nishizawa, O. Onodera, M. Tada, 2014 .

Candesartan prevents arteriopathy progression in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy model.

M. Fukunaga, S. Tsuji, A. Kakita, 2021, The Journal of clinical investigation.

Novel Mutation in EIF2B Gene in a Case of Adult-Onset Leukoencephalopathy with Vanishing White Matter

H. Fukuyama, H. Shibasaki, Y. Miki, 2006, European Neurology.

Patients homozygous and heterozygous for SNCA duplication in a family with parkinsonism and dementia.

A. Kakita, T. Iwatsubo, Hitoshi Takahashi, 2008, Archives of neurology.

Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS

Takashi Inuzuka, Makoto Yoneda, Osamu Onodera, 2014, Neurology.

Botulinum toxin treatment for blepharospasm associated with myasthenia gravis

M. Nishizawa, K. Hara, Keiko Tanaka, 2007, Movement disorders : official journal of the Movement Disorder Society.

Loss of Motor Neurons Innervating Cervical Muscles in Patients With Multiple System Atrophy and Dropped Head

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2018, Journal of neuropathology and experimental neurology.

The FHA domain of aprataxin interacts with the C-terminal region of XRCC1.

S. Tsuji, M. Nishizawa, H. Date, 2004, Biochemical and biophysical research communications.

A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene.

S. Tsuji, M. Nishizawa, Hajime Tanaka, 1996, Human molecular genetics.

Emerging molecular mechanism for cerebral small vessel disease: Lessons from hereditary small vessel disease

M. Nishizawa, O. Onodera, Taisuke Kato, 2015 .

Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic.

Osamu Onodera, Masatoyo Nishizawa, Yoshitaka Nagai, 2008, Human molecular genetics.

Minimal change multiple system atrophy: An aggressive variant?

L. Hazrati, A. Lang, A. Lees, 2015, Movement disorders : official journal of the Movement Disorder Society.

Vocal cord paralysis in myasthenia gravis with anti-MuSK antibodies

M. Tomita, M. Nishizawa, A. Matsuda, 2007, Neurology.

Characteristic features and progression of abnormalities on MRI for CARASIL

M. Tamura, M. Nishizawa, Y. Nishimoto, 2015, Neurology.

A novel mutation in the HTRA1 gene causes CARASIL without alopecia

R. Wennberg, J. Dalmau, A. Kosakai, 2011, Neurology.

Expression of Aquaporin 1 and Aquaporin 4 in the Temporal Neocortex of Patients with Parkinson's Disease

A. Kakita, Y. Ugawa, M. Nishizawa, 2017, Brain pathology.

Case Report: A patient with spinocerebellar ataxia type 31 and sporadic Creutzfeldt-Jakob disease

T. Shimohata, M. Nishizawa, O. Onodera, 2018, Prion.

Quantitative evaluation of brainstem involvement in multiple system atrophy by diffusion-weighted MR imaging

Osamu Onodera, Kenshi Terajima, Masatoyo Nishizawa, 2004, Journal of Neurology.

Globular Glial Mixed Four Repeat Tau and TDP‐43 Proteinopathy with Motor Neuron Disease and Frontotemporal Dementia

A. Kakita, Hitoshi Takahashi, M. Nishizawa, 2016, Brain pathology.

Corticobasal degeneration with focal, massive tau accumulation in the subcortical white matter astrocytes

Shinji Ohara, Masato Hasegawa, Masatoyo Nishizawa, 2006, Acta Neuropathologica.

Chronic bromvalerylurea intoxication: dystonic posture and cerebellar ataxia due to nonsteroidal anti-inflammatory drug abuse.

M. Nishizawa, Y. Takiyama, I. Yanaka, 1998, Internal medicine.

Cognitive impairment and cortical degeneration in neuromyelitis optica

M. Otsuki, A. Kakita, Hitoshi Takahashi, 2013, Annals of neurology.

ピルビン酸ナトリウム療法が有効であったm.3271T>C点変異を有するミトコンドリア病の1例

M. Nishizawa, I. Kawachi, R. Koike, 2015 .

The phenotype spectrum of Japanese multiple system atrophy

A. Kakita, T. Shimohata, K. Wakabayashi, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

A novel two-base mutation in the CuZn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis in Japan

Yasuto Itoyama, Koji Abe, Takafumi Hasegawa, 1996, Neuroscience Letters.

ApoE-isoform-dependent cellular uptake of amyloid-β is mediated by lipoprotein receptor LR11/SorLA.

M. Nishizawa, T. Ikeuchi, A. Koyama, 2015, Biochemical and biophysical research communications.

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.

Parkinsonian features in a patient with diffuse neurofibrillary tangles with calcification (DNTC).

M. Nishizawa, T. Ikeuchi, M. Hirose, 2012, Parkinsonism & related disorders.

A case of cephalic tetanus with facial nerve palsy as an initial symptom in an elderly patient

R. Takagi, T. Shimohata, M. Nishizawa, 2009 .

Differential levels of α-synuclein, β-amyloid42 and tau in CSF between patients with dementia with Lewy bodies and Alzheimer's disease

T. Tokuda, M. Nishizawa, T. Ikeuchi, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Coexistence of Huntington’s disease and amyotrophic lateral sclerosis: a clinicopathologic study

H. Paulson, A. Kakita, M. Wieler, 2012, Acta Neuropathologica.

Difference in MSA phenotype distribution between populations: genetics or environment?

N. Quinn, A. Kakita, A. Lees, 2012, Journal of Parkinson's disease.

[Mitochondrial angiopathy in the cerebral blood vessels of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes)].

T. Miyatake, S. Ohara, M. Nishizawa, 1988, No to shinkei = Brain and nerve.

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.

Clinicopathological features in anterior visual pathway in neuromyelitis optica

A. Kakita, Hitoshi Takahashi, K. Akazawa, 2016, Annals of neurology.

Widespread tissue distribution of multiple mitochondrial DNA deletions in familial mitochondrial myopathy

Y. Kagawa, S. Ohta, M. Nishizawa, 1994, Muscle & nerve.

Variable clinical and neuroimaging features in patients with cerebral amyloid angiopathy–related inflammation

M. Nishizawa, T. Ikeuchi, K. Kasuga, 2015, Alzheimer's & Dementia.

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes

A. Kakita, Hitoshi Takahashi, H. Takebayashi, 2016, Acta neuropathologica communications.

Atypical micrographia associated with corticostriatal white matter lesions in systemic lupus erythematosus

M. Otsuki, M. Nishizawa, J. Shimbo, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes

A. Kakita, Hitoshi Takahashi, H. Takebayashi, 2016, Acta Neuropathologica Communications.

Alzheimer's disease: Report of two autopsy cases with a clinical diagnosis of corticobasal degeneration

Hitoshi Takahashi, M. Nishizawa, K. Okamoto, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

Identification of a SACS gene missense mutation in ARSACS

H. Shimazaki, M. Nishizawa, Y. Takiyama, 2004, Neurology.

Natural course and potential prognostic factors for sleep-disordered breathing in multiple system atrophy.

T. Shimohata, M. Nishizawa, T. Kikuchi, 2017, Sleep medicine.

Daytime sleepiness in Japanese patients with multiple system atrophy: prevalence and determinants

T. Shimohata, M. Nishizawa, M. Tomita, 2012, BMC Neurology.

Novel GFAP mutation in patient with adult‐onset Alexander disease presenting with spastic ataxia

Tomokatsu Yoshida, M. Nakagawa, M. Nishizawa, 2009, Movement disorders : official journal of the Movement Disorder Society.

N. Tanimoto, H. Shiota, K. Miki, 2005, Movement disorders : official journal of the Movement Disorder Society.

Choreiform movements in spinocerebellar ataxia type 1

S. Muramatsu, M. Nishizawa, Y. Takiyama, 2001, Journal of the Neurological Sciences.

Lack of genetic association between TREM2 and late-onset Alzheimer's disease in a Japanese population.

I. Kanazawa, N. Kitamura, T. Asada, 2014, Journal of Alzheimer's disease : JAD.

Characteristics of spinopelvic alignment in Parkinson's disease: Comparison with adult spinal deformity.

T. Shimohata, M. Nishizawa, N. Endo, 2017, Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association.

Chronic T cell leukemia with a NK phenotype reacting with anti-myelin-associated glycoprotein (MAG) mouse monoclonal antibody.

T. Miyatake, S. Sato, T. Inuzuka, 1986, The Tohoku journal of experimental medicine.

[Pathognomonic magnetic resonance imaging (MRI) finding of fluid-fluid level in pyogenic ventriculitis: two case reports].

T. Shimohata, M. Nishizawa, M. Kanazawa, 2014, Rinsho shinkeigaku = Clinical neurology.

Apparent diffusion coefficients distinguish amyotrophic lateral sclerosis from cervical spondylotic myelopathy

T. Shimohata, M. Nishizawa, N. Endo, 2015, Clinical Neurology and Neurosurgery.

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.

Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3.

S. Tsuji, A. Miyashita, R. Kuwano, 2007, Brain : a journal of neurology.

Megacolon in multiple system atrophy: safety concerns related to PEG.

M. Nishizawa, Yuichi Sato, Y. Takado, 2009 .

Five year follow up of a patient with spinal and bulbar muscular atrophy treated with leuprorelin

S. Tsuji, T. Shimohata, M. Nishizawa, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

Relapse of multiple sclerosis in a patient retaining CCR7-expressing T cells in CSF under fingolimod therapy

M. Nishizawa, K. Okamoto, I. Kawachi, 2013, Multiple sclerosis.

A possible variant of neuro-Behçet disease presenting chronic progressive ataxia without mucocutaneo-ocular symptoms

A. Kakita, Hitoshi Takahashi, S. Hayashi, 2006, Rheumatology International.

Significance of gray matter brain lesions in multiple sclerosis and neuromyelitis optica

M. Nishizawa, I. Kawachi, 2015, Neuropathology : official journal of the Japanese Society of Neuropathology.

Gray matter involvement in multiple sclerosis and neuromyelitis optica

M. Nishizawa, I. Kawachi, 2014 .

[Criteria for the diagnosis of corticobasal degeneration].

T. Shimohata, M. Nishizawa, I. Aiba, 2015, Brain and nerve = Shinkei kenkyu no shinpo.

A clinical and pathologic study of a large Japanese family with Machado‐ Joseph disease tightly linked to the DNA markers on chromosome 14q

S. Tsuji, Kayoko Saito, K. Saito, 1994, Neurology.

Evidence for a Common Founder and Clinical Characteristics of Japanese Families with the MAPT R406W Mutation

A. Miyashita, R. Kuwano, T. Imamura, 2011, Dementia and Geriatric Cognitive Disorders Extra.

Recent Advances in Dementia Research

M. Nishizawa, 2016 .

Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems

Osamu Onodera, Masatoyo Nishizawa, M. Nishizawa, 2015, Journal of Neurology, Neurosurgery & Psychiatry.

Maternal anticipation in Machado-Joseph disease (MJD): some maternal factors independent of the number of CAG repeat units may play a role in genetic anticipation in a Japanese MJD family

S. Tsuji, M. Morita, H. Shimazaki, 1998, Journal of the Neurological Sciences.

Clinical features of patients with myasthenia gravis associated with autoimmune diseases

T. Shimohata, M. Nishizawa, Keiko Tanaka, 2007, European journal of neurology.

The measurement and estimation of total energy expenditure in Japanese patients with ALS: a doubly labelled water method study

Toshio Shimizu, T. Komori, K. Ishikawa-Takata, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Diffuse Brain Abnormalities in Myotonic Dystrophy Type 1 Detected by 3.0 T Proton Magnetic Resonance Spectroscopy

T. Nakada, T. Shimohata, M. Nishizawa, 2015, European Neurology.

Sleep disturbance in patients with Parkinson's disease presenting with leg motor restlessness.

T. Shimohata, M. Nishizawa, 2013, Parkinsonism & related disorders.

Treatment responsive opsoclonus–ataxia associated with ovarian teratoma

J. Dalmau, M. Nishizawa, Y. Toyoshima, 2010, Journal of Neurology, Neurosurgery & Psychiatry.

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.

[Successful treatment of neuroborreliosis with combined administration of antibiotics and steroids: a case report].

T. Shimohata, M. Nishizawa, I. Kawachi, 2012, Rinsho shinkeigaku = Clinical neurology.

Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease.

J. Weber, J. Weissenbach, S. Tsuji, 1996, American journal of medical genetics.

Reduced CSF Water Influx in Alzheimer’s Disease Supporting the β-Amyloid Clearance Hypothesis

T. Nakada, I. Kwee, Yukihiro Nakamura, 2015, PloS one.

Cerebral venous sinus thrombosis due to oral contraceptive use: Postmortem 3 T-MRI and autopsy findings

T. Nakada, Y. Fujii, A. Kakita, 2016 .

Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger–Huët anomaly

M. Takagi, A. Miyashita, Hitoshi Takahashi, 2010, Journal of Medical Genetics.

Brainstem metabolites in multiple system atrophy of cerebellar type: 3.0‐T magnetic resonance spectroscopy study

T. Nakada, T. Shimohata, M. Nishizawa, 2011, Movement disorders : official journal of the Movement Disorder Society.

Reversible Hemichorea Caused by Hydrocephalus with Right Sylvian Hematoma Following Subarachnoid Hemorrhage

M. Nishizawa, Y. Takado, T. Ozawa, 2014 .

Dysferlin mutations in Japanese Miyoshi myopathy

Y. Itoyama, I. Nonaka, Kayoko Saito, 2003, Neurology.

[Aberration of the spliceosome in amyotrophic lateral sclerosis].

A. Kakita, M. Nishizawa, O. Onodera, 2014, Rinshō shinkeigaku Clinical neurology.

[Evaluation of two patients with SCA2 with frontal lobe dysfunction using brain SPECT with three-dimensional stereotactic surface projections (3D-SSP)].

T. Shimohata, M. Nishizawa, O. Onodera, 2005, Rinsho shinkeigaku = Clinical neurology.

[Clinical course and serial brain MRI findings in a patient with Lissauer form of general paresis].

T. Shimohata, M. Nishizawa, K. Sanpei, 2015, Rinshō shinkeigaku Clinical neurology.

[Detection of a mutation in mitochondrial DNA in a family with sensorineural deafness and diabetes mellitus as the predominant clinical features].

M. Nishizawa, T. Ishida, Y. Tamagawa, 1995, Nihon Jibiinkoka Gakkai kaiho.

A case of central pontine and extrapontine myelinolysis after surgery for a pituitary tumor.

T. Shimohata, M. Nishizawa, Tomohiko Ishihara, 2017, Rinsho shinkeigaku = Clinical neurology.

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease.

J. Weissenbach, K. Kidd, R. Sherrington, 1995, Human molecular genetics.

Generation of intracellular domain of insulin receptor tyrosine kinase by gamma-secretase.

H. Kaneko, M. Nishizawa, T. Ikeuchi, 2007, Biochemical and Biophysical Research Communications - BBRC.

Correction: SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians

J. Haines, M. Pericak-Vance, G. Schellenberg, 2013, PLoS ONE.

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.

Multiple therapeutic effects of progranulin on experimental acute ischaemic stroke.

T. Nakada, M. Nishihara, T. Shimohata, 2015, Brain : a journal of neurology.

Generation of intracellular domain of insulin receptor tyrosine kinase by γ-secretase

H. Kaneko, M. Nishizawa, T. Ikeuchi, 2007 .

[Longitudinal analysis of age at onset and initial symptoms in patients with amyotrophic lateral sclerosis].

T. Shimohata, M. Nishizawa, Keiko Tanaka, 2006, Rinsho shinkeigaku = Clinical neurology.

A mutation in the immunoproteasome subunit PSMB8 causes autoinflammation and lipodystrophy in humans.

D. Standley, Keiji Tanaka, S. Murata, 2011, The Journal of clinical investigation.

Interleukin-3 promotes neurite outgrowth and elevates choline acetyltransferase activity in vitro.

T. Tabira, M. Nishizawa, T. Kunishita, 1989 .

Submucosal mast cells in the gastrointestinal tract are a target of staphylococcal enterotoxin type A.

K. Omoe, A. Nakane, M. Nishizawa, 2012, FEMS immunology and medical microbiology.

Characteristic features and progression of abnormalities on MRI for CARASIL

M. Tamura, M. Nishizawa, Y. Nishimoto, 2015, Neurology.

Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy

S. Sugano, Yutaka Suzuki, A. Fujiyama, 2018, Nature Genetics.

[Gray matter lesions and cognitive impairment in multiple sclerosis].

M. Nishizawa, I. Kawachi, E. Saji, 2014, Rinsho shinkeigaku = Clinical neurology.

Meiotic instability of the CAG repeats in the SCA6/CACNA1A gene in two Japanese SCA6 families

H. Shimazaki, M. Nishizawa, Y. Takiyama, 2001, Journal of the Neurological Sciences.

Endomyocardial biopsy approach in cases with ventricular arrhythmias.

M. Nishizawa, S. Nunoda, S. Hosoda, 1992, Postgraduate medical journal.

[Acute encephalopathy among patients with renal dysfunction after ingestion of "sugihiratake", angel's wing mushroom--study on the incipient cases in the northern area of Niigata Prefecture].

M. Nishizawa, T. Kuwabara, A. Arai, 2005, Rinsho shinkeigaku = Clinical neurology.

[A patient with HIV encephalopathy presenting with parkinsonism during HAART therapy].

T. Shimohata, M. Nishizawa, Keiko Tanaka, 2006, No to shinkei = Brain and nerve.

Safety and efficacy of thalidomide in patients with POEMS syndrome: a multicentre, randomised, double-blind, placebo-controlled trial

G. Sobue, T. Kanda, J. Kira, 2016, The Lancet Neurology.