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Journal of Neurology|May 20, 2008
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): novel compound heterozygous mutations in the SACS geneS Kamada, S Okawa, T Imota, et al.
No to Shinkei = Brain and Nerve|October 28, 1998
[Muscle atrophy in isolated ACTH deficiency]C Wada, T Imota, K Kato, et al.
Human Genetics|April 17, 1998
Novel mutations of the peripheral myelin protein 22 gene in two pedigrees with Dejerine-Sottas diseaseT Ikegami, H Ikeda, M Aoyama, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 5, 1999
[Hereditary ataxias in Akita prefecture]M Sugawara, I Toyoshima, K Kato, et al.
European Neurology|December 22, 1999
Pontine atrophy in spinocerebellar ataxia type 6M Sugawara, I Toyoshima, C Wada, et al.
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