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Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions.
Takehisa Y, Ujike H, Ishizu H, Terada S, Haraguchi T, Tanaka Y, Nishinaka T, Nobukuni K, Ihara Y, Namba R, Yasuda T, Nishibori M, Hayabara T, Kuroda S. Takehisa Y, et al. Among authors: ihara y. Arch Neurol. 2001 May;58(5):736-40. doi: 10.1001/archneur.58.5.736. Arch Neurol. 2001. PMID: 11346368
A family of familial hypercholesterolemia with cerebral infarction and without coronary heart disease. An unusual case with corneal opacity, polyneuropathy and carpal tunnel syndrome in the family: therapy with probucol and tocopherol nicotinate.
Ihara Y, Nobukuni K, Namba R, Kamisaka K, Kibata M, Kajinami K, Fujita H, Mabuchi H, Shirabe T, Ohshima K, et al. Ihara Y, et al. J Neurol Sci. 1991 Nov;106(1):10-8. doi: 10.1016/0022-510x(91)90187-c. J Neurol Sci. 1991. PMID: 1779233
718 results