Transmission of chronic spongiform encephalopathy with kuru plaques from humans to small rodents

Jun Tateishi, Michiya Ohta, Makoto Koga, +2

Annals of Neurology

Clinical SymptomsCreutzfeldt-jakob DiseaseNeurological DisorderPathologyKuru Plaques +21

Hereditary Sensory Neuropathy, Type II

Michiya Ohta

Archives of Neurology

Rare DiseasesPain SyndromeTemperature DiscriminationNeurological DisorderGenetic Disorder +13

Joseph disease in a non‐Portuguese family

Tetsuo Sakai, Michiya Ohta, Hiroshi Ishino

Neurology

Mendelian DisorderDisease MechanismGenetic DisorderJapanese FamilyGenetics +10

Giant axonal neuropathy

H Igisu, Michiya Ohta, Takeshi Tabira, +3

Neurology

Peripheral Nerve InjuryNeurological DisorderPeripheral NerveNeuromasPrecocious Puberty +15

Ciliated and goblet cells in craniopharyngioma

Toshio Matsushima, Masashi Fukui, Michiya Ohta, +3

Acta Neuropathologica

EpendymaHistopathologyCiliary BodyGoblet CellsAnatomy +2

Astrocytic Deformity and Globular Structures Are Characteristic of the Brains of Patients with Aceruloplasminemia

Kazuma Kaneko, Kunihiro Yoshida, Kunimasa Arima, +5

Journal of Neuropathology & Experimental Neurology

Corticobasal DegenerationNeurological DisorderIron DepositionBrain LesionRedox Biology +21

A quantitative study of the muscle satellite cells in various neuromuscular disorders

S Ishimoto, I Goto, Michiya Ohta, +1

Journal of the Neurological Sciences

Neuromuscular JunctionVarious Neuromuscular DisordersMuscle FunctionSkeletal MuscleNeuroanatomy +11

Clinical observations of juvenile nonprogressive muscular atrophy localized in hand and forearm

Osamu Hashimoto, Masahiro Asada, Michiya Ohta, +1

Journal of Neurology

Thumb HypoplasiaClinical ObservationsMusculoskeletal DisordersMuscle InjuryUpper Extremity +9

Familial occurrence of migraine with a hemiplegic syndrome and cerebellar manifestations

Michiya Ohta, Shukuro Araki, Yoshigoro Kuroiwa

Neurology

Cluster HeadacheCerebellar ManifestationsFamilial OccurrenceNeurological DisorderHemiplegic Syndrome +3

A novel splicing mutation in the ceruloplasmin gene responsible for hereditary ceruloplasmin deficiency with hemosiderosis

Masahide Yazaki, Kunihiro Yoshida, Akinori Nakamura, +6

Journal of the Neurological Sciences

Ceruloplasmin GeneMendelian DisorderGenetic DisorderGeneticsPathogenesis +5