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

מאת Okawa, S, Sugawara, M, Watanabe, S, Toyoshima, I, Imota, T
יצא לאור 2006

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

מאת Obara, Koji, Imota, Tsuyoshi, Mamiya, Shigeo, Toyoshima, Itaru
הוצא לאור ב Case Rep Neurol (2020)