Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Eiichiro Mukai"'
Autor:
Masahiro Iijima, Kazutaka Shiomi, Haruki Koike, Ryoji Nishi, Gen Sobue, Masamitsu Nakazato, Takeshi Yasuda, Tomohiko Nakamura, Masahisa Katsuno, Yukari Date, Eiichiro Mukai, Shohei Ikeda, Yuichi Kawagashira
Publikováno v:
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis. 26(sup1)
Late-onset hereditary (variant) transthyretin (ATTRv) amyloidosis, particularly Val30Met, cases unrelated to endemic foci showed different clinicopathological features compared with early-onset cas...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::810115ca0a76661e93689c3e45055e2e
https://pubmed.ncbi.nlm.nih.gov/31343348
https://pubmed.ncbi.nlm.nih.gov/31343348
Autor:
Hidehiko Konno, Tadashi Wakayama, Satoshi Kuru, Toshiaki Takahashi, Mariko Ito, Jun Shimizu, Mitsuya Morita, Maki Tateyama, Itaru Funakawa, Tohru Ibi, Hiroshi Onodera, Masashi Aoki, Shigeki Kuzuhara, Shoji Tsuji, Takashi Hasegawa, Naoko Shimakura, Yasuto Itoyama, Toshio Saito, Miho Hayasaka, Chikako Yaginuma, Hitomi Sugawara, Emi Abe-Kondo, Gen Sobue, M. Yoshioka, Mineo Yamazaki, Hiroyasu Tanaka, Naoki Suzuki, Hitomi Sato, Toru Kawanami, Naoki Fujii, Eiichiro Mukai, Tsuyoshi Matsumura
Publikováno v:
Journal of Neurology, Neurosurgery, and Psychiatry
Objective and methods Dysferlin encoded by DYSF deficiency leads to two main phenotypes, limb girdle muscular dystrophy (LGMD) 2B and Miyoshi myopathy. To reveal in detail the mutational and clinical features of LGMD2B in Japan, we observed 40 Japane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a015ec4cd4a84158ea156ab01c718e3c
https://doi.org/10.1136/jnnp-2011-301339
https://doi.org/10.1136/jnnp-2011-301339
Autor:
Yuichi Kawagashira, Junko Fujitake, Yukio Ando, Tomohiko Nakamura, Gen Sobue, Masahisa Katsuno, Masahiro Iijima, Eiichiro Mukai, Naoki Hattori, Michiyuki Hayashi, Masahiko Yamamoto, Haruki Koike, Mitsuharu Ueda
Publikováno v:
Journal of the Neurological Sciences. 287:178-184
Late-onset transthyretin Val30Met-associated familial amyloid polyneuropathy (FAP ATTR Val30Met) cases unrelated to endemic foci in Japan show different clinicopathological features from the conventional early-onset cases in endemic foci. We compared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e407ca40af98d6b65838acbf8557f4e2
https://doi.org/10.1016/j.jns.2009.07.028
https://doi.org/10.1016/j.jns.2009.07.028
Autor:
Haruhiko Ohashi, Teruhiko Terasawa, Shigeo Nakamura, Masanori Shimoyama, Eiichiro Mukai, Makoto Utsumi, Keitaro Tsushita
Publikováno v:
International Journal of Hematology. 75:416-420
We report here a patient who developed multiple central nervous system (CNS) space-occupying lesions 6 months after bone marrow transplantation from an HLA-matched unrelated donor. He had extensive chronic graft-versus-host disease and severe thrombo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::822641fde87a61bbba50b983a9d5d9ff
https://doi.org/10.1007/bf02982135
https://doi.org/10.1007/bf02982135
Autor:
Ikuko Aiba, Akiko Tamakoshi, Yuji Abe, Yufuko Saito, Teruhiko Kachi, Masaaki Hirayama, Tetsuo Ando, Shin-ichi Terao, Gen Sobue, Manabu Doyu, Hirohisa Watanabe, Eiichiro Mukai
Publikováno v:
Brain. 125:1070-1083
We investigated the disease progression and survival in 230 Japanese patients with multiple system atrophy (MSA; 131 men, 99 women; 208 probable MSA, 22 definite; mean age at onset, 55.4 years). Cerebellar dysfunction (multiple system atrophy-cerebel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a29f8cd5463b29c7cf35e5512a950ab
https://doi.org/10.1093/brain/awf117
https://doi.org/10.1093/brain/awf117
Autor:
Terunori Mitsuma, Tomoko Morishima, Takeshi Yasuda, Manabu Doyu, Gen Sobue, Eiichiro Mukai, Teruhiko Kachi
Publikováno v:
Journal of the Neurological Sciences. 121:167-171
Plasma levels of testosterone, luteinizing hormone (LH) and follicle-stimulating hormone (FSH) after 3 or 6 days of administration of the synthetic androgenic hormone fluoxymesterone (10 mg/day) were measured in 26 patients with X-linked recessive bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cdba596f5fcf0b479cc0ea899d4041a
https://doi.org/10.1016/0022-510x(94)90347-6
https://doi.org/10.1016/0022-510x(94)90347-6
Autor:
Naoki Atsuta, Saoko Takeshita, Kazumasa Kuniyoshi, Haruki Koike, Masahiro Iijima, Kazutaka Shiomi, Kazuhito Fukui, Hiroaki Adachi, Yasuhisa Toribe, Eiichiro Mukai, Yasuyo Fukada, Takeshi Yasuda, Kenichi Yasui, Yukari Morita, Yasuhiro Hasegawa, Masahiro Horiuchi, Kenji Nakashima, Masahisa Katsuno, Shutaro Takashima, Gen Sobue, Mitsugu Kajiura
Publikováno v:
Brain : a journal of neurology. 133(10)
Acute autonomic and sensory neuropathy is a rare disorder that has been only anecdotally reported. We characterized the clinical, electrophysiological, pathological and prognostic features of 21 patients with acute autonomic and sensory neuropathy. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b1116683ada3ae1247a93a8413848f3
https://pubmed.ncbi.nlm.nih.gov/20736188
https://pubmed.ncbi.nlm.nih.gov/20736188
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 48(3)
Clinical features and courses of 5 cases with HIV encephalopathy were reported. The subjects were among the patients registered as HIV patients at the Nagoya Medical Center, between 1996 and 2005. There were 458 patients with HIV infection including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16384d59aad550d834d77f5497d34732
https://pubmed.ncbi.nlm.nih.gov/18409536
https://pubmed.ncbi.nlm.nih.gov/18409536
Autor:
Terunori Mitsuma, John Q. Trojanowski, T. Kumagai, Yoshio Hashizume, Eiichiro Mukai, Gen Sobue, Takeshi Yasuda
Publikováno v:
Acta Neuropathologica. 79:402-408
Lower motor neurons of the spinal cord of patients with amyotrophic lateral sclerosis (ALS), Werdnig-Hoffmann's disease (WH), X-linked recessive bulbospinal neuronopathy (X-BSNP) and multiple system atrophy (MSA), all of which were known to involve t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37fa830466b80ac143fe5ed3c058692e
https://doi.org/10.1007/bf00308716
https://doi.org/10.1007/bf00308716
Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan
Autor:
Keizo Hirayama, Kunio Tashiro, Seiji Kikuchi, Kenji Nakashima, Jun Ichi Kira, Ichiro Akiguchi, Y Tokumaru, Gen Sobue, Y. Itoyama, Eiichiro Mukai
Publikováno v:
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases. 7(1)
Juvenile muscular atrophy of the distal upper extremity (JMADUE, Hirayama disease) was first reported in 1959 as 'juvenile muscular atrophy of unilateral upper extremity'. Since then, similar patients in their teens or 20s have been described, under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d99054aae9654a8cca46da84560f10c3
https://pubmed.ncbi.nlm.nih.gov/16546758
https://pubmed.ncbi.nlm.nih.gov/16546758