Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tetsuhiko Ikeda"'
Autor:
Takashi Nakajima, Yoshiyuki Sankai, Shinjiro Takata, Yoko Kobayashi, Yoshihito Ando, Masanori Nakagawa, Toshio Saito, Kayoko Saito, Chiho Ishida, Akira Tamaoka, Takako Saotome, Tetsuo Ikai, Hisako Endo, Kazuhiro Ishii, Mitsuya Morita, Takashi Maeno, Kiyonobu Komai, Tetsuhiko Ikeda, Yuka Ishikawa, Shinichiro Maeshima, Masashi Aoki, Michiya Ito, Tatsuya Mima, Toshihiko Miura, Jun Matsuda, Yumiko Kawaguchi, Tomohiro Hayashi, Masahiro Shingu, Hiroaki Kawamoto
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-18 (2021)
Abstract Background Rare neuromuscular diseases such as spinal muscular atrophy, spinal bulbar muscular atrophy, muscular dystrophy, Charcot-Marie-Tooth disease, distal myopathy, sporadic inclusion body myositis, congenital myopathy, and amyotrophic
Externí odkaz:
https://doaj.org/article/ed7f4c135ae64e09a59542a10d0c155d
Autor:
Hideaki Nakatsuji, Tetsuhiko Ikeda, Atsushi Hashizume, Masahisa Katsuno, Gen Sobue, Takashi Nakajima
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Spinal and bulbar muscular atrophy (SBMA), also known as Kennedy's disease, is a rare, slowly progressive, incurable, and hereditary neurodegenerative disease caused by the testosterone-dependent accumulation of pathogenic polyglutamine-expanded andr
Externí odkaz:
https://doaj.org/article/8647819983e14277a1493d98e34429ff
Autor:
Tetsuhiko Ikeda, Tetsuya Takahashi, Mika Tsujita, Masato Kanazawa, Masafumi Toriyabe, Misaki Koyama, Kosuke Itoh, Tsutomu Nakada, Masatoyo Nishizawa, Takayoshi Shimohata
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128844 (2015)
Hypoglycemic encephalopathy (HE) is caused by a lack of glucose availability to neuronal cells, and no neuroprotective drugs have been developed as yet. Studies on the pathogenesis of HE and the development of new neuroprotective drugs have been cond
Externí odkaz:
https://doaj.org/article/1a4774b998eb4d68b28a293b281a845d
Autor:
Shinjiro Takata, Kazuhiro Ishii, Takashi Maeno, Yoko Kobayashi, Yumiko Kawaguchi, Takashi Nakajima, Yoshiyuki Sankai, Takako Saotome, Jun Matsuda, Toshihiko Miura, Michiya Ito, Akira Tamaoka, Kiyonobu Komai, Kayoko Saito, Tetsuhiko Ikeda, Mitsuya Morita, Masashi Aoki, Tetsuo Ikai, Yuka Ishikawa, Tatsuya Mima, Yoshihito Ando, Masahiro Shingu, Tomohiro Hayashi, Hiroaki Kawamoto, Masanori Nakagawa, Shinichiro Maeshima, Hisako Endo, Chiho Ishida, Toshio Saito
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-18 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Rare neuromuscular diseases such as spinal muscular atrophy, spinal bulbar muscular atrophy, muscular dystrophy, Charcot-Marie-Tooth disease, distal myopathy, sporadic inclusion body myositis, congenital myopathy, and amyotrophic lateral s
Autor:
Riki Matsumoto, Yasuko Toyoshima, Akinori Miyashita, Akio Yokoseki, Izumi Aida, Atsushi Ishikawa, Tetsuhiko Ikeda, Hitoshi Takahashi, Osamu Onodera, Masato Kanazawa, Takashi Nakajima, Kento Saito, Takeshi Ikeuchi, Tatsushi Toda, Masatoshi Wakabayashi, Ryoko Takeuchi, Hiroaki Miyahara, Naohiko Seike, Akiyoshi Kakita
Publikováno v:
Movement Disorders. 36:1634-1643
BACKGROUND Mutations in PRKN are the most common cause of autosomal recessive juvenile parkinsonism. The objective of this study was to investigate the association between genotype and pathology in patients with PRKN mutations. METHODS We performed a
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 6, Iss 1, Pp 1-3 (2019)
Human Genome Variation, Vol 6, Iss 1, Pp 1-3 (2019)
Nonsense and frameshift mutations of the dystrophin (DMD) gene usually cause severe Duchenne muscular dystrophy (DMD). Interestingly, however, premature stop codons in exons 1 and 2 result in relatively mild Becker muscular dystrophy (BMD). Herein, w
Autor:
Tetsuhiko Ikeda, Takayoshi Shimohata, Nobuya Fujita, Masato Kanazawa, Masatoyo Nishizawa, Shuichi Igarashi, Hajime Tanaka, Tetsuya Takahashi, Takeo Kuwabara, Aki Sato
Publikováno v:
Diabetes Research and Clinical Practice. 101:159-163
The aim of this study was to investigate factors predicting poor prognosis in patients with hypoglycemic encephalopathy.We retrospectively analyzed data on 165 consecutive patients with hypoglycemic encephalopathy. We evaluated their outcome 1 week a
Autor:
Takayoshi Shimohata, Tetsuhiko Ikeda, Masafumi Toriyabe, Masato Kanazawa, Mika Tsujita, Tetsuya Takahashi, Kosuke Itoh, Misaki Koyama, Tsutomu Nakada, Masatoyo Nishizawa
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128844 (2015)
PLoS ONE
PLoS ONE
Hypoglycemic encephalopathy (HE) is caused by a lack of glucose availability to neuronal cells, and no neuroprotective drugs have been developed as yet. Studies on the pathogenesis of HE and the development of new neuroprotective drugs have been cond
Autor:
Tetsuhiko, Ikeda, Kenju, Hara, Tatsuya, Yamanaka, Hajime, Umezu, Hitoshi, Takahashi, Masatoyo, Nishizawa
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 46(7)
A 63-year-old woman was admitted to our hospital with a 1-month history of visual field defect and reduced bilateral visual acuity. Neurological examination revealed enlargement of bilateral central scotoma and blurred vision, and brain MRI showed ma
Autor:
Masato Kanazawa, Takeo Kuwabara, Hajime Tanaka, Tetsuhiko Ikeda, Shuichi Igarashi, Masatoyo Nishizawa, Tetsuya Takahashi, Aki Sato, Nobuya Fujita, Takayoshi Shimohata
Publikováno v:
Neurology. 78:P07.153-P07.153