M. Takashima

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

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

Inter- and intra-rater reliability in fibroptic endoscopic evaluation of swallowing

Haruka Tohara, Ayako Nakane, Shino Murata et al. · Journal of Oral Rehabilitation · 2010 · 53 citations

Diagnosis, Otorhinolaryngology, Intra-rater Reliability +25

CABS1 Is a Novel Calcium-Binding Protein Specifically Expressed in Elongate Spermatids of Mice1

Akihiro Kawashima, Boran A.H. Osman, M. Takashima et al. · Biology of Reproduction · 2009 · 39 citations · Full text

Spermatogenesis, Fertility, Genetics +17

Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan

Ming Li, Kinya Ishikawa, Shuta Toru et al. · Journal of Human Genetics · 2003 · 29 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8