H. Shimazaki

发表

Physiological properties of projection neurons in the monkey striatum to the globus pallidus

M. Kimura, M. Kato, H. Shimazaki, 2004, Experimental Brain Research.

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

S. Tsuji, H. Shimazaki, Y. Fukuda, 2012, Journal of Medical Genetics.

Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutation

S. Tsuji, Kunihiro Yoshida, S. Ikeda, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Characteristics of aged ischemic stroke patients indicative of cardioembolism

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of Thrombosis and Thrombolysis.

Tissue Plasminogen Activator to Treat a Stroke after Foam Sclerotherapy in a Woman with a Patent Foramen Ovale.

H. Shimazaki, T. Ozawa, R. Koide, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Successful Tissue Plasminogen Activator for a Patient with Stroke After Stanford Type A Aortic Dissection Treatment.

H. Shimazaki, T. Ozawa, R. Koide, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Reversible limbic encephalitis with antibodies against the membranes of neurones of the hippocampus

J. Dalmau, H. Shimazaki, I. Nakano, 2009, BMJ Case Reports.

Left thalamus infarction in the thalamotuberal artery perfusion area causing subcortical diaschisis and transcortical sensory aphasia

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of the Neurological Sciences.

A large family with spinocerebellar ataxia type 6 in Iran: a clinical and genetic study.

H. Shimazaki, Y. Takiyama, I. Nakano, 2008, Archives of Iranian medicine.

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

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

A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia

H. Shimazaki, Y. Takiyama, K. Koh, 2022, Human Genome Variation.

A new simple method using carotid duplex ultrasonography to assess intracranial vertebrobasilar arterial stenosis

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of the Neurological Sciences.

Spinocerebellar Degeneration, Multiple System Atrophy and Progressive Supranuclear Palsy: —Transition of the Disease Concepts and Differential Diagnosis for Spinal Cord Disease and Parkinson Disease—@@@—疾患概念の変遷と, 脊髄疾患ならびにParkinson病との鑑別—

H. Shimazaki, I. Nakano, 2012 .

16q-linked autosomal dominant cerebellar ataxia: A clinical and genetic study

H. Shimazaki, T. Amino, H. Mizusawa, 2006, Journal of the Neurological Sciences.

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

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

Adult-onset Alexander disease with typical "tadpole" brainstem atrophy and unusual bilateral basal ganglia involvement: a case report and review of the literature

H. Shimazaki, Y. Takiyama, K. Sakoe, 2010, BMC neurology.

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects

H. Shimazaki, Y. Takiyama, 2012 .

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.

Chapter 2 Lysosomal Dysfunctions in Hereditary Spastic

H. Shimazaki, 2018 .

Lysosomal Dysfunctions in Hereditary Spastic Paraplegias

H. Shimazaki, 2017 .

Polymerase chain reaction-based analysis using deaminated DNA of dodecamer expansions in CSTB, associated with Unverricht-Lundborg myoclonus epilepsy.

W. Tian, H. Shimazaki, K. Umetsu, 2005, Genetic testing.

Catastrophic Secondary Infarctions with Onset Seizure Following Tissue Plasminogen Activator Therapy.

H. Shimazaki, T. Ozawa, R. Koide, 2019, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Unique combination of hyperintense vessel sign on initial FLAIR and delayed vasoconstriction on MRA in reversible cerebral vasoconstriction syndrome: A case report

H. Shimazaki, M. Namekawa, I. Nakano, 2014, Cephalalgia : an international journal of headache.

Novel compound heterozygous mutations in sacsin-related ataxia

S. Sakoda, H. Shimazaki, Y. Takiyama, 2005, Journal of the Neurological Sciences.

Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment

S. Tsuji, H. Shimazaki, H. Ishiura, 2018, Journal of Human Genetics.

Chédiak–Higashi syndrome presenting as a hereditary spastic paraplegia

H. Shimazaki, H. Ishiura, Y. Takiyama, 2021, Journal of Human Genetics.

Clinical Aspects of Anti-NMDA Receptor Encephalitis

H. Shimazaki, 2011 .

The Rapid Effectiveness of Minocycline against Scrub Typhus Meningoencephalitis.

H. Shimazaki, T. Naoi, M. Sawada, 2016, Internal medicine.

Paraneoplastic anti–N‐methyl‐D‐aspartate receptor encephalitis associated with ovarian teratoma

Josep Dalmau, W. Mason, M. Dichter, 2007, Annals of neurology.

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

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

Limited Wegener's granulomatosis manifested by abducens nerve palsy resulting from pachymeningitis.

M. Morita, H. Shimazaki, I. Nakano, 2006, Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases.

S. Hamada, S. Tsuji, H. Shimazaki, 2019, Molecular genetics & genomic medicine.

Spinocerebellar ataxia type 14 caused by a nonsense mutation in the PRKCG gene

Naoaki Saito, H. Shimazaki, Shigeru Tanaka, 2019, Molecular and Cellular Neuroscience.

[A case of aceruloplasminemia presenting as cerebellar ataxia with homozygous mutation nt2602 delG].

H. Shimazaki, H. Miyajima, Y. Takiyama, 2004, No to shinkei = Brain and nerve.

Reversible limbic encephalitis with antibodies against the membranes of neurones of the hippocampus

J. Dalmau, H. Shimazaki, I. Nakano, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

Akinesis of the apex similar to takotsubo cardiomyopathy following tetanus

H. Shimazaki, T. Ozawa, R. Koide, 2019, Journal of the Neurological Sciences.

"Hot cross bun" sign associated with SCA1.

H. Shimazaki, M. Namekawa, J. Honda, 2015, Internal medicine.

Mutations in the mitochondrial gene C12ORF65 lead to syndromic autosomal recessive intellectual disability and show genotype phenotype correlation.

A. Ekici, R. Abou Jamra, A. Reis, 2013, European journal of medical genetics.

Middle Cerebellar Peduncles and Pontine T2 Hypointensities in ARSACS

H. Shimazaki, M. Baba, Y. Takiyama, 2013, Journal of neuroimaging : official journal of the American Society of Neuroimaging.

An unusual case of a spasticity-lacking phenotype with a novel SACS mutation

H. Shimazaki, Y. Takiyama, K. Sakoe, 2007, Journal of the Neurological Sciences.

H. Shimazaki, Y. Takiyama, K. Sakoe, 2006, Neurology.

Relapsing polychondritis coupling with cerebral amyloid deposit inducing cerebral amyloid angiopathy-related inflammation

H. Shimazaki, T. Ozawa, R. Koide, 2020, Journal of Thrombosis and Thrombolysis.

Identification of a SACS gene missense mutation in ARSACS

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

A novel adult case of juvenile-onset Alexander disease: complete remission of neurological symptoms for over 12 years, despite insidiously progressive cervicomedullary atrophy

H. Shimazaki, Y. Takiyama, K. Sakoe, 2011, Neurological Sciences.

Novel SACS mutation in a Belgian family with sacsin-related ataxia

N. Janin, H. Shimazaki, Y. Takiyama, 2008, Journal of the Neurological Sciences.

S. Sakoda, M. Nakamori, H. Shimazaki, 2006, Journal of Neurology.

A phenotype without spasticity in sacsin-related ataxia

H. Shimazaki, Y. Takiyama, K. Sakoe, 2005, Neurology.

Inverse ocular bobbing in a patient with encephalitis associated with antibodies to the N-methyl-D-aspartate receptor.

M. Morita, J. Dalmau, H. Shimazaki, 2008, Archives of neurology.

[An autopsy case of origin-unidentified meningeal carcinomatosis presenting with monoradiculopathy multiplex in the lower extremities].

M. Morita, H. Shimazaki, Y. Takiyama, 2005, Rinsho shinkeigaku = Clinical neurology.

Diagnostic Value of Neurophysiological Evaluation in Patients with ARSACS

H. Shimazaki, Y. Takiyama, J. Fukae, 2015 .

Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay

H. Shimazaki, M. Baba, Y. Takiyama, 2012, Clinical Neurology and Neurosurgery.

Spastic Paraplegias Due to Non-Traumatic Spinal Cord Disorders

H. Shimazaki, 2017, Essentials of Spinal Cord Injury Medicine.

Prevalence of elevated serum anti-N-methyl-D-aspartate receptor antibody titers in patients presenting exclusively with psychiatric symptoms: a comparative follow-up study

T. Shimada, H. Shimazaki, S. Kato, 2016, BMC Psychiatry.

Noteworthy Cardiovascular Involvement with Sporadic Late-onset Nemaline Myopathy

K. Kario, I. Nishino, H. Shimazaki, 2021, Internal medicine.

Vertical Gaze Palsy Caused by Selective Unilateral Rostral Midbrain Infarction

H. Shimazaki, T. Ozawa, R. Koide, 2018, Neuro-ophthalmology.

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.

Chédiak–Higashi syndrome presenting as a hereditary spastic paraplegia

H. Shimazaki, H. Ishiura, Y. Takiyama, 2021, Journal of human genetics.

Late-onset autosomal recessive cerebellar ataxia and neuropathy with a novel splicing mutation in the ATM gene.

H. Shimazaki, I. Nakano, S. Fujimoto, 2020, Journal of integrative neuroscience.

[Clinical aspects of hereditary spastic paraplegias].

H. Shimazaki, 2014, Rinsho shinkeigaku = Clinical neurology.

Management Effort for Delirium and Insomnia in Patients with Acute Ischemic Stroke (MEDIAS) Study

H. Shimazaki, T. Ozawa, R. Koide, 2020, Psychiatry and Clinical Neurosciences.

Neural information transferred from the putamen to the globus pallidus during learned movement in the monkey.

K Watanabe, M. Kimura, N. Matsumoto, 1996, Journal of neurophysiology.

Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairment

S. Tsuji, H. Shimazaki, H. Ishiura, 2018, Journal of Human Genetics.

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.

Unilateral posterior reversible encephalopathy syndrome: A case report

K. Kawai, H. Shimazaki, T. Ozawa, 2019, Clinical Neurology and Neurosurgery.