Kazuo Yoshizawa

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

Kinya Ishikawa, Hajime Tanaka, Masaaki Saito et al. · The American Journal of Human Genetics · 1997 · 150 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +6

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

Kinya Ishikawa, Masahiko Watanabe, Kazuo Yoshizawa et al. · Journal of Neurology Neurosurgery & Psychiatry · 1999 · 117 citations · Full text

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

Hiroki Takahashi, Kinya Ishikawa, Takeshi Tsutsumi et al. · Journal of Human Genetics · 2004 · 95 citations · Full text

Mendelian Disorder, Neurological Disorder, Genetic Disorder +7

A gene on <i>SCA4</i> locus causes dominantly inherited pure cerebellar ataxia

Utako Nagaoka, M. Takashima, Kinya Ishikawa et al. · Neurology · 2000 · 83 citations

Association between Catechol-&lt;i&gt;O&lt;/i&gt;-Methyltransferase Gene Polymorphisms and Wearing-Off and Dyskinesia in Parkinson’s Disease

Miho Watanabe, Satoru Harada, Takashi Nakamura et al. · Neuropsychobiology · 2003 · 64 citations