Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fumiko Isa"'
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 62:629-632
The mechanism of mirror movements in two patients was investigated; one with congenital mirror movement, the other with schizencephaly. Transcranial magnetic stimulation on one side elicited motor evoked potentials (MEPs) in their thenar muscles on b
Autor:
Takeshi Ikeuchi, Reiji Koide, Hajime Tanaka, Osamu Onodera, Shuichi Igarashi, Hitoshi Takahashi, Rui Kondo, Atsushi Ishikawa, Akemi Tomoda, Teruhisa Miike, null Keiko Sato, Yuetsu Ihara, Toshiyuki Hayabara, Fumiko Isa, Hitoshi Tanabe, Susumu Tokiguchi, Masataka Hayashi, Natsue Shimizu, Fusahiro Ikuta, Haruhiko Naito, Shoji Tsuji
Publikováno v:
Annals of Neurology. 37:769-775
Dentatorubral-pallidoluysian atrophy is an autosomal dominant neurodegenerative disease characterized by various combinations of ataxia, choreoathetosis, myoclonus, epilepsy, and dementia as well as a wide range of ages at onset. A specific unstable
Autor:
Masaharu Hayashi, Kei Shioda, Masao Minagawa, Yoshio Morimatsu, Fumiko Isa, Masahiro Itoh, Kimiko Tamagawa, Masaya Oda
Publikováno v:
Braindevelopment. 21(5)
Both xeroderma pigmentosum group A (XPA) and Cockayne syndrome (CS) are rare autosomal disorders, have a genetic defect in the step of nucleotide repair, and involve various neurological abnormalities caused by progressive neurodegeneration. We perfo
Autor:
Hiroshi Tsukagoshi, Takashi Kanda, Masaya Oda, Ryouichi Hanakago, Kimiko Tamagawa, Mihoko Yonezawa, Fumiko Isa
Publikováno v:
Brain : a journal of neurology. 113
The pathology of the peripheral nervous system (PNS) in 2 autopsied cases of group A xeroderma pigmentosum (De Sanctis Cacchione syndrome) are presented. Motor nerves including those of the oculomotor systems were severely affected, but involvement o
Publikováno v:
Electroencephalography and Clinical Neurophysiology/Electromyography and Motor Control. 97:S143