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American Journal of Human Genetics|April 1, 1996
Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosisT Ikeuchi, S Igarashi, Y Takiyama, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 1, 1999
[Recent advances in the studies on Alzheimer's diseases]S Tsuji
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 1, 1999
[Advances in understanding of clinical presentations and molecular mechanisms of triplet repeat diseases]S Tsuji
Journal of Neural Transmission. Supplementum|December 29, 2000
Dentatorubral-pallidoluysian atrophy (DRPLA)S Tsuji
Folia Histochemica Et Cytobiologica|June 2, 1998
Electron microscopic localization of acetylcholinesterase activity in the central nervous system: chemical basis of a catalytic activity of Hatchett's brown (cupric ferrocyanide) precipitate revealed by 3,3'-diaminobenzidineS Tsuji
Histochemistry|January 1, 1984
Koelle's copper thiocholine method performed with a low-pH phosphate buffer, followed by osmification of the precipitate: revival of two abandoned proceduresS Tsuji
Journal of Microscopy|September 1, 1980
A method for obtaining cryo-ultramicrotome sections of 35 nm thickness monitored by myofibrillar fine structureS Tsuji
Rinsho Shinkeigaku = Clinical Neurology|December 1, 1994
[Transcranial magnetic stimulation]S Tsuji
Human Molecular Genetics|September 15, 1999
A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?R Koide, S Kobayashi, T Shimohata, et al.
American Journal of Human Genetics|August 1, 1997
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13.1-p13.2 and are strongly associated with mild CAG expansions in the spinocerebellar ataxia type 6 gene in chromosome 19p13.1K Ishikawa, H Tanaka, M Saito, et al.
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