Murata Miho
Publications by Year
Research Areas
Legal and Regulatory Analysis, Linguistic, Cultural, and Literary Studies, Military Technology and Strategies, Genetic Neurodegenerative Diseases, Parkinson's Disease Mechanisms and Treatments
Most-Cited Works
- → Variants associated with Gaucher disease in multiple system atrophy(2015)101 cited
- → Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses(2014)68 cited
- → Differential Diagnosis Tool for Parkinsonian Syndrome Using Multiple Structural Brain Measures(2013)10 cited
- → Studies on DNA markers (D4S10 and D4S43/S127) genetically linked to Huntington's disease in Japanese families(1990)7 cited
- → Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy(2016)5 cited
- プリオン病のサーベイランスと感染予防に関する調査研究 他院でM232Rの診断がついた6年後にはじめて頭部MRI DWIで高信号を認めた62歳女性症例(2015)
- Familial spinocerebellar ataxia with sensory neuropathy associated with compound heterozygous intermediate CAG expansions in MJD locus(2016)
- パーキンソン病 V.特論 J-PPMI(パーキンソン病発症予防のための運動症状発症前バイオマーカーの特定研究)(2017)
- Mutational analysis of causative genes for autosomal recessive spinocerebellar degeneration (SCD) to delineate molecular epidemiology of early-onset SCD(2016)
- 高齢者における神経変性疾患 1.パーキンソン病の薬物治療(2016)