MediFind found 7 doctor with experience in Hereditary Ataxia near Ishikawa, JP. Of these, 7 are Experienced.
Kosuke Matsuzono practices in Shimotsuke, Japan. Mr. Matsuzono is rated as an Experienced expert by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Creutzfeldt-Jakob Disease, Gerstmann-Straussler-Scheinker Syndrome, Stroke, Dementia, and Endovascular Embolization.
Shigeru Fujimoto practices in Tochigi, Japan. Mr. Fujimoto is rated as an Experienced expert by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Stroke, Atrial Fibrillation, Cerebelloolivary Atrophy, Thrombectomy, and Deep Brain Stimulation.
Masahide Goto practices in Tochigi, Japan. Goto is rated as an Experienced expert by MediFind in the treatment of Hereditary Ataxia. Their top areas of expertise are Temple Syndrome, Rommen Mueller Sybert Syndrome, Campomelia Cumming Type, and Campomelic Dysplasia.
Noriki Okada practices in Shimotsuke, Japan. Okada is rated as an Experienced expert by MediFind in the treatment of Hereditary Ataxia. Their top areas of expertise are Neonatal Hemochromatosis, Congenital Hepatic Fibrosis, Biliary Atresia, Liver Transplant, and Pancreaticoduodenectomy.
Takafumi Mashiko practices in Tochigi, Japan. Mashiko is rated as an Experienced expert by MediFind in the treatment of Hereditary Ataxia. Their top areas of expertise are Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease), Primary Lateral Sclerosis, Stroke, Cerebral Hypoxia, and Endovascular Embolization.
Reiji Koide practices in Tochigi, Japan. Koide is rated as an Experienced expert by MediFind in the treatment of Hereditary Ataxia. Their top areas of expertise are Cerebelloolivary Atrophy, Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease), Primary Lateral Sclerosis, Multiple System Atrophy, and Endovascular Embolization.
Masayuki Yamada practices in Tochigi, Japan. Mr. Yamada is rated as an Experienced expert by MediFind in the treatment of Hereditary Ataxia. His top areas of expertise are Spinocerebellar Ataxia Type 31, Anemia, and Hereditary Ataxia.
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Last Updated: 10/30/2025