Zobrazeno 1 - 10
of 59
pro vyhledávání: '"Tomohiro, Kumada"'
Autor:
Yuji Kanazawa, Yasuhisa Kurata, Miki Nagai, Kenji Inoue, Fumihito Nozaki, Atsushi Mori, Mariko Ishihara, Mioko Mori, Tomohiro Kumada, Minoru Shibata, Takeo Kato, Masako Nakai, Makoto Kano
Publikováno v:
BMC Surgery, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Surgery to prevent aspiration has complications related to tracheostomy tube, such as the trachea-brachiocephalic artery fistula. Glottic closure procedure makes tracheostoma at a position higher than the first ring of the trachea
Externí odkaz:
https://doaj.org/article/9447d749442243809c12e9bd5f08acc4
Autor:
Yu Hiramatsu, Yuji Okamoto, Akiko Yoshimura, Jun-Hui Yuan, Masahiro Ando, Yujiro Higuchi, Akihiro Hashiguchi, Eiji Matsuura, Fumihito Nozaki, Tomohiro Kumada, Kei Murayama, Mikiya Suzuki, Yuki Yamamoto, Naoko Matsui, Yoshimichi Miyazaki, Masamitsu Yamaguchi, Youji Suzuki, Jun Mitsui, Hiroyuki Ishiura, Masaki Tanaka, Shinichi Morishita, Ichizo Nishino, Shoji Tsuji, Hiroshi Takashima
Publikováno v:
Journal of Neurology. 269:4129-4140
Mitochondrial disorders are a group of clinically and genetically heterogeneous multisystem disorders and peripheral neuropathy is frequently described in the context of mutations in mitochondrial-related nuclear genes. This study aimed to identify t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f893b211b0287b22986e09af4ce16b
https://doi.org/10.1007/s00415-022-11026-w
https://doi.org/10.1007/s00415-022-11026-w
Autor:
Mamiko Yamada, Hisato Suzuki, Katsuyuki Matsui, Yoshihiro Maruo, Kenjiro Kosaki, Fumihito Nozaki, Tomohiro Kumada, Kenji Inoue, Minoru Shibata, Mioko Mori
Publikováno v:
Brain and Development. 43:724-728
Background The MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity) syndrome, which is caused by a hemizygous variant in the EIF2S3 gene on chromosome Xp22, is associated with significant morbidit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04c27847803dc65f43df38bc7ac11097
https://doi.org/10.1016/j.braindev.2021.02.002
https://doi.org/10.1016/j.braindev.2021.02.002
Publikováno v:
Pediatrics International. 64
A growing number of studies have demonstrated the efficacy of high-flow nasal cannula therapy (HFNC) for treating children with acute respiratory distress. However, it remains unknown whether HFNC is effective in bedridden patients with acute respira
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c06311cbcb452b2c003568571bcde14
https://doi.org/10.1111/ped.14756
https://doi.org/10.1111/ped.14756
Autor:
Yuji Kanazawa, Yasuhisa Kurata, Miki Nagai, Kenji Inoue, Fumihito Nozaki, Atsushi Mori, Mariko Ishihara, Mioko Mori, Tomohiro Kumada, Minoru Shibata, Takeo Kato, Masako Nakai, Makoto Kano
Publikováno v:
BMC Surgery, Vol 22, Iss 1, Pp 1-8 (2022)
Background Surgery to prevent aspiration has complications related to tracheostomy tube, such as the trachea-brachiocephalic artery fistula. Glottic closure procedure makes tracheostoma at a position higher than the first ring of the trachea and theo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3f585278c332a4e0815e28f19d7d00f
https://pubmed.ncbi.nlm.nih.gov/35148723
https://pubmed.ncbi.nlm.nih.gov/35148723
Autor:
Eri Takeshita, Mioko Mori, Fumihito Nozaki, Hiroyuki Yajima, Yasuyuki Iwata, Tomohiro Kumada, Tatsuya Fujii
Publikováno v:
Brain and Development. 41:796-802
Objectives Quantitative or semiquantitative outcome measures for patients with Duchenne muscular dystrophy (DMD) are important, as they can be objective indicators of the natural history of DMD; these measures also aid in the evaluation of the effica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55ac16de976c112fb1fa2e602c2b9e0a
https://doi.org/10.1016/j.braindev.2019.06.002
https://doi.org/10.1016/j.braindev.2019.06.002
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 28:2453-2458
Background: Although the incidence of cerebral infarction is higher in Duchenne muscular dystrophy (.75 per 100) than in the general population (7.5-11.4 per 100 000), only 18 cases have been reported, and prevention and management guidelines for inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3275d198370bb72d031bc1eabe66773
https://doi.org/10.1016/j.jstrokecerebrovasdis.2019.06.023
https://doi.org/10.1016/j.jstrokecerebrovasdis.2019.06.023
Autor:
Ryuichi Nishii, Toshinori Hirai, Tatsuya Fujii, Tomohiro Kumada, Tatsuya Higashi, Shinya Kagawa, Yoshihiko Kishibe, Masaaki Takahashi, Hiroshi Yamauchi, Chio Okuyama, Shigeki Nagamachi
Publikováno v:
Imaging in Medicine. 10(1):9-16
Objectives :- A ketogenic diet (KD) is a strict dietary protocol that incorporates high-fat, low-protein, and low-carbohydrate foods. Increasing the levels of ketones became an eventual and effective treatment strategy for medically refractory epilep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87762136a7692677f2205888ea7a9c50
https://repo.qst.go.jp/records/49010
https://repo.qst.go.jp/records/49010
Autor:
Anri Hayashi, Minoru Shibata, Tatsuya Fujii, Fumihito Nozaki, Takashi Kusunoki, Ikuko Hiejima, Tomohiro Kumada
Publikováno v:
American Journal of Medical Genetics Part A. 173:1947-1950
Left ventricular noncompaction cardiomyopathy (LVNC) is characterized by prominent trabecular meshwork, and it is thought to result from arrest of the normal compaction process during embryogenesis. Patients with LVNC may be asymptomatic or have symp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::130f5d3cced3413e51d00b9a30fd0382
https://doi.org/10.1002/ajmg.a.38270
https://doi.org/10.1002/ajmg.a.38270
Autor:
Makiko Saitoh, Naoko Nishimura, Nobusuke Kimura, Masashi Mizuguchi, Tomohiro Kumada, Fumihito Nozaki, Yoshihisa Higuchi, Ai Hoshino
Publikováno v:
Pediatrics International. 58:1215-1218
Most childhood cases of acute necrotizing encephalopathy (ANE) involve neither family history nor recurrence. ANE occasionally occurs, however, as a familial disorder or recurs in Caucasian patients. A mutation of RAN-binding protein 2 (RANBP2) has b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d83adc221daced54d2b8eab91ea0279
https://doi.org/10.1111/ped.13119
https://doi.org/10.1111/ped.13119