Norio Ohkoshi

Autoimmunity to Gephyrin in Stiff-Man Syndrome

Margaret H. Butler, Akito Hayashi, Norio Ohkoshi et al. · Neuron · 2000 · 213 citations · Full text

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

Quantitation of amyloid beta-protein (A beta) in the cortex during aging and in Alzheimer's disease.

Hiromasa Funato, Masahiro Yoshimura, Kaoru Kusui et al. · PubMed · 1998 · 146 citations

An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains

Kinya Ishikawa, Shuta Toru, Taiji Tsunemi et al. · The American Journal of Human Genetics · 2005 · 128 citations · Full text

Neurodegenerative Diseases, Neurobiology Of Disease, Mendelian Disorder +13

An Association between Idiopathic Parkinson's Disease and Polymorphisms of Phase II Detoxification Enzymes: Glutathione S-Transferase M1 and Quinone Oxidoreductase 1 and 2

Shoji Harada, Chieko Fujii, Akito Hayashi et al. · Biochemical and Biophysical Research Communications · 2001 · 125 citations

Idiopathic Parkinson, Biochemistry, Medicine +8