H. Sasaki

发表

Deep brain stimulation of subthalamic area for severe proximal tremor

M. Kitagawa, S. Kikuchi, K. Tashiro, 2000, Neurology.

Vocal cord abductor paralysis in spinocerebellar ataxia type 1

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

GNE mutations causing distal myopathy with rimmed vacuoles with inflammation

S. Kikuchi, K. Tashiro, H. Sasaki, 2003, Neurology.

Impact of screening with thyroid ultrasonography in myasthenia gravis patients

S. Kikuchi, H. Sasaki, M. Niino, 2012, Acta neurologica Scandinavica.

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

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

Central phenotype and related varieties of spinocerebellar ataxia 2 (SCA2): a clinical and genetic study with a pedigree in the Japanese

K. Tashiro, H. Sasaki, H. Sasaki, 1996, Journal of the Neurological Sciences.

Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study.

Í. Lopes-Cendes, S. Tsuji, A. Brice, 2001, American journal of human genetics.

Mapping of the gene for Machado-Joseph disease within a 3.6-cM interval flanked by D14S291/D14S280 and D14S81, on the basis of studies of linkage and linkage disequilibrium in 24 Japanese families.

T. Yoshiki, H. Sasaki, T. Hamada, 1995, American journal of human genetics.

Spinocerebellar ataxia 1 (SCAl) in the Japanese in Hokkaido may derive from a single common ancestry

T. Yoshiki, K. Tashiro, H. Sasaki, 2022 .

Genetics of multiple sclerosis.

S. Kikuchi, K. Tashiro, H. Sasaki, 2000, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Electrophysiological features of central motor conduction in spinocerebellar atrophy type 1, type 2, and Machado-Joseph disease

T. Yuasa, H. Sasaki, H. Sasaki, 1998, Journal of neurology, neurosurgery, and psychiatry.

Spastin gene mutation in Japanese with hereditary spastic paraplegia

K. Tashiro, H. Sasaki, H. Sasaki, 2002, Journal of medical genetics.

[Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].

K. Tashiro, H. Sasaki, I. Yabe, 1998, Rinsho shinkeigaku = Clinical neurology.

[Spinocerebellar ataxia type 5 (SCA5)].

K. Tashiro, H. Sasaki, 1999, Ryoikibetsu shokogun shirizu.

Antineutrophil cytoplasmic antibodies and the optic-spinal form of multiple sclerosis in Japan.

S. Kikuchi, K. Tashiro, H. Sasaki, 1996, Journal of neurology, neurosurgery, and psychiatry.

Effect of High Fat Diet on NKT Cell Function and NKT Cell‐mediated Regulation of Th1 Responses

L. Kaer, S. Kikuchi, K. Iwabuchi, 2008, Scandinavian journal of immunology.

Skeletal myoclonus in olivopontocerebellar atrophy

K. Tashiro, H. Sasaki, T. Hamada, 1987, Neurology.

HLA-DPB1*0501 is not uniquely associated with opticospinal multiple sclerosis in Japanese patients. Important role of DPB1*0301

S. Kikuchi, H. Sasaki, I. Yabe, 2006, Multiple sclerosis.

Both the HLA-CPB1 and -DRB1 alleles correlate with risk for multiple sclerosis in Japanese: clinical phenotypes and gender as important factors.

J. Kira, S. Kikuchi, K. Tashiro, 2000, Tissue antigens.

The hereditary spinocerebellar ataxias in Japan

K. Tashiro, H. Sasaki, H. Sasaki, 2003, Cytogenetic and Genome Research.

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans

H. Zoghbi, T. Ashizawa, M. Pandolfo, 2002, Neurology.

A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.

M. Pericak-Vance, G. Schellenberg, K. Tashiro, 1998, Genomics.

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.

Correlation between DJ-1 levels in the cerebrospinal fluid and the progression of disabilities in multiple sclerosis patients

H. Ariga, H. Sasaki, M. Hirotani, 2008, Multiple sclerosis.

Caveolin‐3 gene mutation in Japanese with rippling muscle disease

S. Kikuchi, K. Tashiro, H. Sasaki, 2003, Acta neurologica Scandinavica.

Clinical features and natural history of spinocerebellar ataxia type 1

K. Tashiro, H. Sasaki, H. Sasaki, 1996, Acta neurologica Scandinavica.

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.

Heat shock protein 70 gene polymorphism in Japanese patients with multiple sclerosis.

S. Kikuchi, K. Tashiro, H. Sasaki, 2001, Tissue antigens.

[Frequencies of triplet repeat disorders in dominantly inherited spinocerebellar ataxia (SCA) in the Japanese].

K. Tashiro, H. Sasaki, 1999, Nihon rinsho. Japanese journal of clinical medicine.

Erdheim-Chester disease and slowly progressive cerebellar dysfunction.

K. Tashiro, H. Sasaki, T. Hamada, 1995, Journal of neurology, neurosurgery, and psychiatry.

The clinical and genetic spectrum of spinocerebellar ataxia 14

H. Zoghbi, T. Bird, R. Margolis, 2005, Neurology.

Increasing prevalence and incidence of multiple sclerosis in northern Japan

S. Kikuchi, H. Sasaki, M. Niino, 2008, Multiple sclerosis.

Spinocerebellar ataxia type 1 and familial spontaneous pneumothorax

S. Kikuchi, K. Tashiro, H. Sasaki, 1997, Neurology.

Myelopathy due to osteochondroma: MR and CT studies.

H. Abe, K. Tashiro, F. Moriwaka, 1990, Journal of computer assisted tomography.

[A case of chronic bromvalerylurea intoxication with episodic neurological manifestations such as optic neuropathy ophthalmoplegia and ataxia].

K. Tashiro, H. Sasaki, T. Hamada, 1996, Rinsho shinkeigaku = Clinical neurology.

Recessively inherited spastic paraplegia associated with ataxia, congenital cataracts, thin corpus callosum and axonal neuropathy

S. Kikuchi, K. Tashiro, H. Sasaki, 2000, Acta neurologica Scandinavica.

Clinical trial of acetazolamide in SCA6, with assessment using the Ataxia Rating Scale and body stabilometry

K. Tashiro, H. Sasaki, I. Yabe, 2001, Acta neurologica Scandinavica.

Dissociation of smooth pursuit and vestibulo-ocular reflex cancellation in SCA-6

K Fukushima, Y Inuyama, K. Fukushima, 2000, Neurology.

The role of B cells in multiple sclerosis: implications for B-cell-targeted therapy.

H. Sasaki, M. Hirotani, M. Niino, 2010, Current Medicinal Chemistry.

Characterization of the γc chain among 27 unrelated Japanese patients with X-linked severe combined immunodeficiency (X-SCID)

T. Morio, H. Takada, K. Sugamura, 2000, Human Genetics.

Expansion of CD4+CD28− T cells producing high levels of interferon-γ in peripheral blood of patients with multiple sclerosis

S. Kikuchi, H. Sasaki, K. Iwabuchi, 2008, Multiple sclerosis.

Genomic HLA profiles of MS in Hokkaido, Japan: important role of DPB1*0501 allele

S. Kikuchi, K. Tashiro, H. Sasaki, 2000, Journal of Neurology.

Relationship between Barkhof criteria and the clinical features of multiple sclerosis in northern Japan

H. Sasaki, M. Nakamura, M. Niino, 2009, Multiple sclerosis.

The significance of oligoclonal bands in multiple sclerosis in Japan: Relevance of immunogenetic backgrounds

S. Kikuchi, K. Tashiro, H. Sasaki, 1998, Journal of the Neurological Sciences.

CSF pleocytosis and expansion of spinal lesions in Japanese Multiple sclerosis with special reference to the new diagnostic criteria

S. Kikuchi, K. Tashiro, H. Sasaki, 2005, Journal of Neurology.

Baló's concentric sclerosislike lesion in the brainstem of a multiple sclerosis patient

S. Kikuchi, H. Sasaki, I. Yabe, 2008, Journal of 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.

[Clinical study of gene locus heterogeneity in hereditary olivopontocerebellar atrophy (OPCA)--report of 2 pedigrees affected with non SCA1 type OPCA].

K. Tashiro, H. Sasaki, A. Wakisaka, 1991, Rinshō shinkeigaku Clinical neurology.

Dominantly inherited leukodystrophy showing cerebellar deficits and spastic paraparesis: a new entity?

S. Kikuchi, K. Tashiro, H. Sasaki, 1997, Journal of Neurology.

[Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes].

H. Sasaki, 1993, Rinsho shinkeigaku = Clinical neurology.

Disruption of facial affect processing in word deafness

F. Moriwaka, H. Sasaki, C. Clarke, 2004, Journal of Neurology, Neurosurgery & Psychiatry.

[Periodic alternating nystagmus in spinocerebellar ataxia type 6 (SCA 6)].

K. Tashiro, H. Sasaki, I. Yabe, 1998, Rinsho shinkeigaku = Clinical neurology.

Disruption of facial affect processing in word deafness

F. Moriwaka, H. Sasaki, K. Tashiro, 2004, Journal of Neurology Neurosurgery & Psychiatry.