A novel sacsin mutation in a Japanese woman showing clinical uniformity of autosomal recessive spastic ataxia of Charlevoix‐Saguenay

par Okawa, S, Sugawara, M, Watanabe, S, Toyoshima, I, Imota, T
Publié 2006

The Effectiveness of Perampanel for Myoclonic Seizures in Down Syndrome with Isodicentric Chromosome 21

par Obara, Koji, Imota, Tsuyoshi, Mamiya, Shigeo, Toyoshima, Itaru
Publié dans Case Rep Neurol (2020)