A Japanese case of steroid responsive myopathy with deficient chondroitin sulphate

Por Yabe, I, Kikuchi, S, Higashi, T, Tashiro, K, Maruo, Y
Publicado em 2002

Spastin gene mutation in Japanese with hereditary spastic paraplegia

Por Yabe, I, Sasaki, H, Tashiro, K, Matsuura, T, Takegami, T, Satoh, T
Publicado em 2002

Twenty CAG repeats are sufficient to cause the SCA6 phenotype

Por Komeichi, K., Sasaki, H., Yabe, I., Yamashita, I., Kikuchi, S., Tashiro, K.
Publicado em 2001

Vocal cord abductor paralysis in spinocerebellar ataxia type 1

Por SHIOJIRI, T, TSUNEMI, T, MATSUNAGA, T, SASAKI, H, YABE, I, TASHIRO, K, NISHIZAWA, N, TAKAMOTO, K, YOKOTA, T, MIZUSAWA, H
Publicado em 1999

A case of acute urinary retention caused by periaqueductal grey lesion

Por Yaguchi, H, Soma, H, Miyazaki, Y, Tashiro, J, Yabe, I, Kikuchi, S, Sasaki, H, Kakizaki, H, Moriwaka, F, Tashiro, K
Publicado em 2004

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

Por Yabe, I, Sasaki, H, Yamashita, I, Tashiro, K, Takei, A, Suzuki, Y, Kida, H, Takiyama, Y, Nishizawa, M, Hokezu, Y, Nagamatsu, K, Oda, T, Ohnishi, A, Inoue, I, Hata, A
Publicado em 2001