Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Yumi Horigome"'
Autor:
Yumi Horigome, Yusuke Okada, Nobuyoshi Ishikawa, Nobuaki Iwasaki, Hitoshi Takita, Motohiro Sato, Kenzo Hamano, Takao Enomoto
Publikováno v:
Journal of Epilepsy. 11:195-201
To evaluate whether arachnoid cysts (ACs) can directly cause epilepsy by cortical compression, we studied the relationships among seizures, the volume of ACs, and regional cerebral blood perfusion around ACs. Subjects were 11 patients (10.5 ± 7.2 ye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94e422a6e73c10b29a43a847221ffaf2
https://doi.org/10.1016/s0896-6974(98)00017-6
https://doi.org/10.1016/s0896-6974(98)00017-6
Autor:
Toshiki Takeya, Tadao Nose, Junko Nakayama, Kenzo Hamano, Yusuke Okada, Hitoshi Takita, Yumi Horigome, Nobuaki Iwasaki
Publikováno v:
Neuroradiology. 39:841-846
We devised a three-dimensional method for estimation of cerebral development and myelination which measures cerebral volume using MRI. Accuracy of the system was estimated using cadaver brains. The mean percentage error in the calculated volumes comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6395e2c1a0d892874567f5635b8fb5eb
https://doi.org/10.1007/s002340050517
https://doi.org/10.1007/s002340050517
Publikováno v:
Journal of the Japan Epilepsy Society. 13:195-201
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e5509b1be54a37857815829535c434b
https://doi.org/10.3805/jjes.13.195
https://doi.org/10.3805/jjes.13.195
Autor:
Akira Matsui, Nobuaki Iwasaki, Satoko Nakahara, Yae Shimakura, Emiko Noguchi, Tadao Arinami, Kimiko Yamakawa-Kobayashi, Masayasu Ohta, Junko Nakayama, Yumi Horigome, C. Nakahara, Nao Yamamoto, Junko Shiono, Kenzo Hamano
Publikováno v:
Neuroscience Letters. 329:249-251
The voltage-gated sodium channel type II alpha polypeptide gene (SCN2A) R188W mutation with channel dysfunction was recently identified in a patient with febrile and afebrile seizures. A possible association between SCN2A R19K polymorphism and febril
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f1723b23f939fd32b72bf8aab7c80bb
https://doi.org/10.1016/s0304-3940(02)00651-1
https://doi.org/10.1016/s0304-3940(02)00651-1
Publikováno v:
Neuroscience Research. 71:e269
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea370ee6fd84993fa452989f9c7cbc9b
https://doi.org/10.1016/j.neures.2011.07.1175
https://doi.org/10.1016/j.neures.2011.07.1175
Publikováno v:
Journal of Arrhythmia. 27:BPB_4
Introduction:Dravet syndrome (DS) is a severe type of childhood epilepsies, in which SCN1A mutation is found in 80% of cases. Sudden unexpected death in epilepsy (SUDEP) is frequently seen in DS, but its mechanisms remain unknown. We electrophysiolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac5c4d3e79cd4c51dae1f7ae41129156
https://doi.org/10.4020/jhrs.27.bpb_4
https://doi.org/10.4020/jhrs.27.bpb_4
Autor:
Takesaburo Ogata, Chiaki Hirano, Ryo Sumazaki, Tomohiro Kamoda, Hitoshi Takita, Natsue Kataoka, Yoji Nagai, Ichiro Ono, Takashi Hanada, Eiji Yamamura, Kenji Shin, Chiaki Moriyama, Kenzo Hamano, Takao Ehara, Yumi Horigome
Publikováno v:
Journal of pediatric gastroenterology and nutrition. 9(2)
Six of seven children with fulminant hepatitis (FH) were treated with a combination of twice daily plasmapheresis and intensive conservative therapy including special amino acid solution, glucagon-insulin therapy, dexamethasone, and so on. The remain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f02ffc2baa64ac1e8587ad88cad7d81
https://pubmed.ncbi.nlm.nih.gov/2509666
https://pubmed.ncbi.nlm.nih.gov/2509666
Publikováno v:
Annual Review of Hydrocephalus ISBN: 9783662111512
We experienced a case of holoprosencephaly associated with endocrine abnormalities. A male neonate, one of twins, was born at 36 weeks of gestation. The other twin had no abnormalities. At birth, our case weighed 2,780g, had dyspnea and was immediate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6ff15dbac9d562ef2ca61c54a80d0a6
https://doi.org/10.1007/978-3-662-11149-9_87
https://doi.org/10.1007/978-3-662-11149-9_87
Osteonecrosis of vertebrae in a child with acute lymphocytic leukaemia during L-asparaginase therapy
Publikováno v:
European journal of pediatrics. 149(3)
We report a child with acute lymphocytic leukaemia who developed simultaneous osteonecrosis of vertebrae and cerebral thrombosis during L-asparaginase therapy. Fibrinogen, antithrombin III and plasminogen were decreased. Fresh frozen plasma in additi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c231eff88bc04d1955e0df0b1b0d41f
https://pubmed.ncbi.nlm.nih.gov/2612502
https://pubmed.ncbi.nlm.nih.gov/2612502
Autor:
Nobuaki Iwasaki, Yukako Yokouchi, Satoko Nakahara, Junko Nakayama, Tatsuyuki Ohto, Takuo Migita, Hideo Hamaguchi, Takeshi Aoki, Takako Maki, Hisako Saitoh, Kenzo Hamano, Masahiro Kikuchi, Akira Matsui, Ryuta Tanaka, Yumi Horigome, Tadao Arinami, Makoto Hasegawa
Publikováno v:
Scopus-Elsevier
Febrile seizures (FSs) represent the most common form of childhood seizure. In the Japanese population, the incidence rate is as high as 7%. It has been recognized that there is a significant genetic component for susceptibility to this type of seizu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::958499192e59a33afe1e0205fcfa7070
http://www.scopus.com/inward/record.url?eid=2-s2.0-17344375789&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-17344375789&partnerID=MN8TOARS