ISHIKAWA Kinya | Department of Neurology and Neurological Science, Tokyo Medical and Dental University Graduate Schoo

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著作論文

A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6
A Case of Multiple Sclerosis with Homonymous Hemianopia Examined by Positron Emission Tomography
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano
A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia
Direct and accurate measurement of CAG repeat configuration in the ataxin-1 (ATXN-1) gene by "dual-fluorescence labeled PCR-restriction fragment length analysis"
Analyses of copy number and mRNA expression level of the α-synuclein gene in multiple system atrophy
On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCA

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