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

od Okawa, S, Sugawara, M, Watanabe, S, Toyoshima, I, Imota, T
Izdano 2006

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

od Obara, Koji, Imota, Tsuyoshi, Mamiya, Shigeo, Toyoshima, Itaru
Izdano u Case Rep Neurol (2020)