T. Hamada

发表

Central nervous system infection and immune response in mice inoculated into the lip with herpes simplex virus type 1

P. Doherty, U. Schumacher, L. Kastrukoff, 1982, Journal of Neuroimmunology.

A progressive neurodegenerative disorder with cortical spongiform change and white matter damage presenting with pseudobulbar palsy

K. Tashiro, F. Moriwaka, A. Takei, 1997 .

Myoclonus and Seizures in a Patient with Parkinsonism: Induction by Levodopa and Its Confirmation on SEPs

K. Tashiro, F. Moriwaka, T. Matsuura, 1993, The Japanese journal of psychiatry and neurology.

[Magnetic resonance imaging in Parkinson's disease--the evaluation of the width of pars compacta on T2 weighted image].

K. Miyasaka, K. Tashiro, F. Moriwaka, 1992, Rinshō shinkeigaku Clinical neurology.

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.

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

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

Mercury and selenium contents in amyotrophic lateral sclerosis in Hokkaido, the northernmost island of Japan

H. Satoh, F. Moriwaka, T. Hamada, 1993, Journal of the Neurological Sciences.

Genetics of multiple sclerosis.

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

Dementia with ALS features and diffuse Pick body-like inclusions (atypical Pick's disease?).

K. Tashiro, N. Yoshimura, T. Hamada, 1995, Clinical neuropathology.

Two cases of neoplastic angioendotheliomatosis presenting with myelopathy

M. Satoh, K. Nagashima, K. Tashiro, 1991, Neurology.

The aetiology of mirror writing: a new hypothesis.

K. Tashiro, F. Moriwaka, T. Hamada, 1987, Journal of neurology, neurosurgery, and psychiatry.

Cytomegalovirus Isolation from a Chimpanzee with Acute Demyelinating Disease After Inoculation of Multiple Sclerosis Brain Cells

L. Rorke, E. Huang, Z. Wróblewska, 1979, Infection and immunity.

Multiphasic demyelinating disorder with acute transverse myelitis in Japanese

S. Kikuchi, K. Tashiro, I. Yabe, 2003, Journal of Neurology.

Multiphasic demyelinat- ing disorder with acute transverse myelitis

S. Kikuchi, K. Tashiro, I. Yabe, 2003 .

Acute transverse myelopathy in multiple sclerosis

K. Tashiro, F. Moriwaka, T. Hamada, 1990, Journal of the Neurological Sciences.

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

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

HTLV-1 associated myelopathy combined with chronic thyroiditis.

K. Tashiro, T. Hamada, T. Yanagihara, 1991, Journal of internal medicine.

HTLV‐I‐associated myelopathy: Oligoclonal immunoglobulin G bands contain anti‐HTLV‐I p24 antibody

L. Grimaldi, R. Roos, K. Tashiro, 1988, Annals of neurology.

Association of vitamin D receptor gene polymorphism with multiple sclerosis in Japanese

K. Miyasaka, S. Kikuchi, K. Tashiro, 1999, Journal of the Neurological Sciences.

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.

Skeletal myoclonus in olivopontocerebellar atrophy

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

The role of CD4(+) or CD8(+) T cells in the protective immune response of BALB/c mice to Neospora caninum infection.

K. Fujisaki, H. Nagasawa, T. Mikami, 2000, Veterinary parasitology.

A variant of encephalomeningocele: heterotopic brain tissue on the scalp.

T. Hamada, T. Tanii, 1984, Dermatologica.

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.

Facial palsy in multiple sclerosis

K. Tashiro, F. Moriwaka, T. Hamada, 1997, Journal of Neurology.

S. Kikuchi, K. Tashiro, S. Hashimoto, 2003, Neurology.

HLA profiles of multiple sclerosis in Hokkaido, the northernmost island of Japan

K. Tashiro, F. Moriwaka, T. Hamada, 1992, Acta neurologica Scandinavica.

Multiple sclerosis in Hokkaido, the northernmost island of Japan: prospective analyses of clinical features.

K. Tashiro, F. Moriwaka, T. Hamada, 1992, Internal medicine.

[MRI changes in spontaneous intracranial hypotension].

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

Anti-nuclear antibodies and the optic-spinal form of multiple sclerosis

K. Miyasaka, S. Kikuchi, K. Tashiro, 1997, Journal of Neurology.

Sequential magnetic resonance features of encephalopathy induced by systemic mastocytosis.

K. Tashiro, F. Moriwaka, M. Musashi, 1994, Internal medicine.

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.

Positional vertigo and macroscopic downbeat positioning nystagmus in spinocerebellar ataxia type 6 (SCA6)

K. Fukushima, K. Tashiro, H. Sasaki, 2003, Journal of Neurology.

CTLA-4 gene polymorphism may modulate disease in Japanese multiple sclerosis patients

K. Miyasaka, S. Kikuchi, K. Tashiro, 1999, Journal of the Neurological Sciences.

Erdheim-Chester disease and slowly progressive cerebellar dysfunction.

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

Spinocerebellar ataxia type 1 and familial spontaneous pneumothorax

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

Treatment of cerebellar ataxia with 5-HT1A agonist

H. Sasaki, I. Yabe, A. Takei, 2008, The Cerebellum.

Effects of Tandospirone on “5-HT1A Receptor-Associated Symptoms” in Patients with Machado-Josephe Disease: An Open-Label Study

K. Tashiro, H. Sasaki, I. Yabe, 2004, Clinical neuropharmacology.

Spinocerebellar ataxia 1 (SCA1) in the Japanese: Analysis of CAG trinucleitide repeat expansion and instability of the repeat for paternal transmission

T. Yoshiki, K. Tashiro, H. Sasaki, 1995, Japanese Journal of Human Genetics.

Phenotype variation correlates with CAG repeat length in SCA2 - A study of 28 Japanese patients 1 Presented in part at the 122nd annual meeting of the American Neurological Association, San Diego, Cal, Sep–Oct, 1997. 1

S. Tsuji, T. Yuasa, K. Tashiro, 1998, Journal of the Neurological Sciences.

[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.

Autosomal dominant spastic paraplegia linked to chromosome 2p: clinical and genetic studies of a large Japanese pedigree

K. Tashiro, F. Moriwaka, H. Sasaki, 1997, Journal of the Neurological Sciences.

Serum carnitine and disabling fatigue in multiple sclerosis

S. Kikuchi, K. Tashiro, H. Sasaki, 1996, Psychiatry and clinical neurosciences.

Anticardiolipin antibodies in Japanese patients with multiple sclerosis

T. Koike, K. Tashiro, F. Moriwaka, 1993, Acta neurologica Scandinavica.

Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6)

H. Sawa, K. Tashiro, H. Sasaki, 1998, Acta Neuropathologica.

Syringomyelic syndrome: clinical features in 31 cases confirmed by CT myelography or magnetic resonance imaging

H. Abe, Y. Iwasaki, K. Tashiro, 1987, Journal of Neurology.

Mosaicism of unstable CAG repeats in the brain of spinocerebellar ataxia type 2

K. Tashiro, H. Sasaki, I. Yabe, 1999, Journal of Neurology.

CAG repeat expansion of Machado-Joseph disease in the Japanese: analysis of the repeat instability for parental transmission, and correlation with disease phenotype

T. Yoshiki, K. Tashiro, H. Sasaki, 1995, Journal of the Neurological Sciences.

Genetic heterogeneity of dominantly inherited olivopontocerebellar atrophy (OPCA) in the Japanese: Linkage study of two pedigrees and evidence for the disease locus on chromosome 12q (SCA2)

T. Yoshiki, K. Tashiro, H. Sasaki, 1994, The Japanese Journal of Human Genetics.

Dropped head sign as the only symptom of myasthenia gravis.

H. Yaguchi, A. Takei, T. Hamada, 2007, Internal medicine.

S. Kikuchi, K. Tashiro, H. Sasaki, 2004, Journal of the Neurological Sciences.

Estrogen receptor gene polymorphism and multiple sclerosis in Japanese patients: interaction with HLA-DRB1*1501 and disease modulation

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Journal of Neuroimmunology.

Motor neuron disease and past poliomyelitis

K. Tashiro, F. Moriwaka, N. Takahata, 2004, Journal of Neurology.

Motor neuron disease and past poliomyelitis. Geographic study in Hokkaido, the northern-most island of Japan. ALS Study Group.

K. Tashiro, F. Moriwaka, N. Takahata, 1993, Journal of neurology.

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

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

Prevalence of Parkinson's disease in Hokkaido, the northernmost island of Japan.

S. Kikuchi, K. Tashiro, F. Moriwaka, 1996, Internal medicine.

CTLA-4 gene polymorphism is not associated with conventional multiple sclerosis in Japanese

S. Kikuchi, H. Sasaki, I. Yabe, 2005, Journal of Neuroimmunology.

Cerebrospinal fluid IgG profiles and multiple sclerosis in Japan

K. Tashiro, F. Moriwaka, T. Hamada, 1993, Acta neurologica Scandinavica.

Serum melatonin levels and insomnia in patients with Machado-Joseph Disease

M. Okawa, H. Sasaki, I. Yabe, 2004 .

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.

[An autopsy case of amyotrophic lateral sclerosis associated with cervical syringomyelia].

K. Tashiro, H. Fukaura, T. Isu, 1990, No to shinkei = Brain and nerve.

SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia

A. Ohnishi, K. Tashiro, H. Sasaki, 1998, Journal of the Neurological Sciences.

Beneficial effects of tandospirone on ataxia of a patient with Machado‐Joseph disease

K. Tashiro, I. Yabe, A. Takei, 2002, Psychiatry and clinical neurosciences.

HTLV-I-Associated Myelopathy: Oligoclonal Immunoglobdn

L. Grimaldi, R. Roos, K. Tashiro, 2004 .

Multisystem degeneration

M. Kase, K. Tashiro, T. Hamada, 1986, Neurology.

Difference in the Effects of Tandospirone on Ataxia in Various Types of Spinocerebellar Degeneration: An Open-Label Study

K. Tashiro, A. Takei, S. Hamada, 2010, The Cerebellum.

‘Drug holiday’ effects of tandospirone in a patient with Machado–Joseph disease

K. Tashiro, I. Yabe, A. Takei, 2003, Psychiatry and clinical neurosciences.

[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, Rinsho shinkeigaku = Clinical neurology.

Linkage study of dominantly inherited olivo-ponto-cerebellar atrophy (OPCA) and Holmes' ataxia

M. Yoshida, K. Tashiro, H. Sasaki, 1988, Japanese Journal of Human Genetics.

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

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

Estrogen receptor gene polymorphism and multiple sclerosis in Japanese patients: interaction with HLA-DRB1*1501 and disease modulation

S. Kikuchi, K. Tashiro, I. Yabe, 2002, Journal of Neuroimmunology.

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.

MRI findings of multiple sclerosis with acute transverse myelopathy

Kazuo Miyasaka, K. Miyasaka, K. Tashiro, 1992, Journal of the Neurological Sciences.

A case of POEMS syndrome associated with reactive amyloidosis and Waldenström's macroglobulinaemia

Y. Kihara, I. Yoshikawa, T. Hamada, 2002, Journal of internal medicine.

[Linkage study of hereditary olivopontocerebellar atrophy: genetic evidence for locus heterogeneity in Japanese cases].

K. Tashiro, H. Sasaki, A. Wakisaka, 1992, Rinsho shinkeigaku = Clinical neurology.