Kunihiro Yoshida
Kanazawa University(JP)Japan Monkey Centre(JP)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, Trace Elements in Health, Neurological diseases and metabolism, Neuroinflammation and Neurodegeneration Mechanisms
Most-Cited Works
- → A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans(1995)461 cited
- → Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease(2000)252 cited
- → Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a japanese family(1995)247 cited
- → Clinical and genetic characterization of adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia associated with CSF1R mutation(2016)174 cited
- → An X-ray structural study of human ceruloplasmin in relation to ferroxidase activity(1997)128 cited
- → Biotransformation of nitric oxide.(1987)110 cited
- Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic cases.