MIZUSAWA Hidehiro | Department of Neurology and Neurological Science, Tokyo Medical and Dental University

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著作論文

Geographic Difference of Mortality of Creutzfeldt-Jakob Disease in Japan
Aging of the human limbic system: Observations of centenarian brains and analyses of genetic risk factors for senile changes
A clinical and genetic study in a large cohort of patients with spinocerebellar ataxia type 6
Physical map and haplotype analysis of 16q-linked autosomal dominant cerebellar ataxia (ADCA) type III in Japan
Immunohistochemical Diagnosis of Cryptococcus neoformans var. gattii Infection in Chronic Meningoencephalitis : the First Case in Japan
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano
Ultrastructural and MRI study of the substantia nigra evolving exofocal post-ischemic neuronal death in the rat
TNF-related apoptosis-inducing ligand (TRAIL) induces neuronal apoptosis in HIV-encephalopathy
Coexistence of CJD and Alzheimer's disease : An autopsy case showing typical clinical features of CJD
UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase in nuclei and rimmed vacuoles of muscle fibers in DMRV (distal myopathy with rimmed vacuoles)
A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan
Introduction of Short Interfering RNA to Silence Endogenous E-Selectin in Vascular Endothelium Leads to Successful Inhibition of Leukocyte Adhesion
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia
Two region-dependent pathways of eosinophilic neuronal death after transient cerebral ischemia
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
Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from elderly patients with Alzheimer's disease
Predominant motor symptoms in a 74-year-old man with a small elongation in the spinocerebellar atrophy type 1 gene
Significant increase in the expression of matrix metalloproteinase 7 in primary CNS lymphoma

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