H Nagatomo

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene

Hidetoshi Date, Osamu Onodera, Hajime Tanaka et al. · Nature Genetics · 2001 · 382 citations

New Hit, Mendelian Disorder, Ophthalmology +10

Corticobasal degeneration: widespread argentophilic threads and glia in addition to neurofibrillary tangles. Similarities of cytoskeletal abnormalities in corticobasal degeneration and progressive supranuclear palsy

Tatsuya Takahashi, Naoji Amano, Tokiji Hanihara et al. · Journal of the Neurological Sciences · 1996 · 45 citations

Neurodegenerative Diseases, Corticobasal Degeneration, Neuroanatomy +10

Asymmetrical temporal lobe atrophy with massive neuronal inclusions in multiple system atrophy

Katsuhiko Shibuya, H Nagatomo, K Iwabuchi et al. · Journal of the Neurological Sciences · 2000 · 38 citations

Neurodegenerative Diseases, Neuropsychology, Corticobasal Degeneration +13

Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) and diabetes mellitus: molecular genetic analysis and family study

Hideki Onishi, Ken Inoue, Hitoshi Osaka et al. · Journal of the Neurological Sciences · 1993 · 32 citations

Mitochondrial Myopathy, Metabolic Syndrome, Lactic Acidosis +8

Immunohistochemical expression of microtubule-associated protein 5 (MAP5) in glial cells in multiple system atrophy

Nobutaka Arai, Masaki Nishimura, Masaya Oda et al. · Journal of the Neurological Sciences · 1992 · 31 citations

Signal Transduction, Microtubule-associated Protein 5, Glial Cells +9