K. Uekawa

发表

Structural proteins of the opaque muscle fibers in Duchenne muscular dystrophy

M. Uchino, S. Araki, O. Yoshida, 1985, Neurology.

[A hereditary ataxia associated with hypoalbuminemia and hyperlipidemia--a variant form of Friedreich's disease or a new clinical entity?].

T. Yuasa, K. Uekawa, S. Kawasaki, 1992, Rinsho shinkeigaku = Clinical neurology.

High single-dose alternate-day corticosteroid regimens in treatment of polymyositis

M. Uchino, S. Araki, O. Yoshida, 2004, Journal of Neurology.

Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial

Y. Itoyama, S. Tsuji, G. Sobue, 2017, The Lancet Neurology.

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

S. Sugano, S. Tsuji, T. Yuasa, 2001, Nature Genetics.

[A case report of oculo-pharyngo-distal type myopathy, with vacuolar degeneration and myelin figure in muscle fibers (author's transl)].

M. Uchino, H. Tokuomi, K. Uekawa, 1979, Rinsho shinkeigaku = Clinical neurology.

Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15q13–15

H. Utsumi, H. Takashima, Hajime Tanaka, 2000, Annals of neurology.

Single muscle fiber analysis of myoclonus epilepsy with ragged‐red fibers

E. Uyama, T. Kumamoto, K. Uekawa, 1998, Muscle & nerve.

Decision making of amyotrophic lateral sclerosis patients on noninvasive ventilation to receive tracheostomy positive pressure ventilation

Y. Ando, M. Uchino, S. Yamashita, 2014, Clinical Neurology and Neurosurgery.

Correlation between urinary incontinence and psychosis in patients with advanced‐stage Parkinson’s disease

K. Nakahara, S. Nakane, T. Ikeda, 2020 .