Mizusawa Hidehiro | Department Of Neurology And Neurological Science (chairman: Prof. Hidehiro Mizusawa) Graduate School

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概要

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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
Skeletal Muscle MRI in Complex Regional Pain Syndrome
Classification of Cerebellar Atrophy Using Voxel-based Morphometry and SPECT with an Easy Z-score Imaging System
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
Fatal Encephalitis in a Case of Hypereosinophilic Syndrome: MRI and Autopsy Findings
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
The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures
Dura mater graft-associated Creutzfeldt-Jakob disease in Japan : Clinicopathological and molecular characterization of the two distinct subtypes
Predominant motor symptoms in a 74-year-old man with a small elongation in the spinocerebellar atrophy type 1 gene
Effects of pericyte and various cytokines on integrity of endothelial monolayer originated from blood-nerve barrier : An in vitro study
Morel's laminar sclerosis showing apraxia of speech : Distribution of cortical lesions in an autopsy case
Differential diagnosis of CNS lymphomatoid granulomatosis
Anticholinergic Drugs and Cognitive Functions
Alternative BSE Risk Assessment Methodology of Imported Beef and Beef Offal to Japan
Significant increase in the expression of matrix metalloproteinase 7 in primary CNS lymphoma
5-FU-induced Acute Leukoencephalopathy
Duration of Prion Disease is Longer in Japan Than in Other Countries
Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage
Efficient in vivo delivery of antisense oligonucleotide to choroid plexus
Chronic Inflammatory Demyelinating Polyradiculoneuropathy in a Patient with Crohn's Disease
Metronidazole-induced Encephalopathy
Bilateral Facial Nerve Palsy Caused by a Metastatic Malignant Lymphoma
Progression of Bilateral Internal Carotid Artery Dissection during Antiplatelet Therapy
Intramedullary Spinal Cord Metastasis with a Longitudinally Extensive Spinal Cord Lesion
Pseudoradicular Sensory Loss Caused by a Cerebral Demyelinative Lesion

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