Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Sanae Kawakami"'
Autor:
Kenji Yamada, Hideaki Shiraishi, Eishin Oki, Mika Ishige, Toshiyuki Fukao, Yusuke Hamada, Norio Sakai, Fumihiro Ochi, Asami Watanabe, Sanae Kawakami, Kazuyo Kuzume, Kenji Watanabe, Koji Sameshima, Kiyotaka Nakamagoe, Akira Tamaoka, Naoko Asahina, Saki Yokoshiki, Takashi Miyakoshi, Kota Ono, Koji Oba, Toshiyuki Isoe, Hiroshi Hayashi, Seiji Yamaguchi, Norihiro Sato
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 15, Iss , Pp 55-63 (2018)
Introduction: Fatty acid oxidation disorders (FAODs) are rare diseases caused by defects in mitochondrial fatty acid oxidation (FAO) enzymes. While the efficacy of bezafibrate, a peroxisome proliferator-activated receptor agonist, on the in vitro FAO
Externí odkaz:
https://doaj.org/article/36d7a86db88242389cb8b2cc33a34d39
Autor:
Hideaki Shiraishi, Kenji Yamada, Eishin Oki, Mika Ishige, Toshiyuki Fukao, Yusuke Hamada, Norio Sakai, Fumihiro Ochi, Asami Watanabe, Sanae Kawakami, Kazuyo Kuzume, Kenji Watanabe, Koji Sameshima, Kiyotaka Nakamagoe, Akira Tamaoka, Naoko Asahina, Saki Yokoshiki, Takashi Miyakoshi, Koji Oba, Toshiyuki Isoe, Hiroshi Hayashi, Seiji Yamaguchi, Norihiro Sato
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 20, Iss , Pp - (2019)
Introduction: Fatty acid oxidation disorders (FAODs) are rare diseases caused by a defective mitochondrial fatty acid oxidation (FAO) enzyme. We recently reported that bezafibrate improved patient quality of life (QOL) based on the SF-36 questionnair
Externí odkaz:
https://doaj.org/article/485479e07814483c920b57c0dc96b489
Autor:
Koji Oba, Seiji Yamaguchi, Naoko Asahina, Saki Yokoshiki, Sanae Kawakami, Kiyotaka Nakamagoe, Mika Ishige, Toshiyuki Isoe, Kiyoshi Egawa, Koji Sameshima, Norihiro Sato, Fumihiro Ochi, Kazuyo Kuzume, Akira Tamaoka, Kenji Yamada, Hideaki Shiraishi, Asami Watanabe, Kenji Watanabe, Keiko Kobayashi, Hiroshi Hayashi, Takashi Miyakoshi
Publikováno v:
Brain and Development. 43:214-219
Background Very long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is a mitochondrial fatty acid oxidation disorder that causes episodic attacks, such as general fatigue, hypotonia, myalgia, and rhabdomyolysis accompanied by lack of energy. As yet
Autor:
Hironori Kobayashi, Kenji Yamada, Fumihiro Ochi, Yuko Matsubara, Asami Watanabe, Kozue Kuwabara, Takeshi Taketani, Seiji Fukuda, Keiichi Matsubara, Yuichi Mushimoto, Yuki Hasegawa, Seiji Yamaguchi, Sanae Kawakami
Publikováno v:
JIMD Reports, Vol 49, Iss 1, Pp 17-20 (2019)
JIMD Reports
JIMD Reports
Very long‐chain acyl‐CoA dehydrogenase (VLCAD) deficiency is an autosomal recessive mitochondrial fatty acid oxidation disorder that manifests in three clinical forms: (a) severe, (b) milder, and (c) myopathic. Patients with the myopathic form pr
Autor:
Asami Watanabe, Yusuke Hamada, Saki Yokoshiki, Kenji Watanabe, Kiyotaka Nakamagoe, Takashi Miyakoshi, Hideaki Shiraishi, Norihiro Sato, Fumihiro Ochi, Seiji Yamaguchi, Naoko Asahina, Kota Ono, Toshiyuki Isoe, Koji Oba, Toshiyuki Fukao, Mika Ishige, Hiroshi Hayashi, Norio Sakai, Kazuyo Kuzume, Akira Tamaoka, Kenji Yamada, Eishin Oki, Koji Sameshima, Sanae Kawakami
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 15, Iss, Pp 55-63 (2018)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Introduction: Fatty acid oxidation disorders (FAODs) are rare diseases caused by defects in mitochondrial fatty acid oxidation (FAO) enzymes. While the efficacy of bezafibrate, a peroxisome proliferator-activated receptor agonist, on the in vitro FAO
Autor:
Toshiyuki Fukao, Mika Ishige, Hiroshi Hayashi, Hideaki Shiraishi, Asami Watanabe, Takashi Miyakoshi, Koji Oba, Yusuke Hamada, Seiji Yamaguchi, Norihiro Sato, Fumihiro Ochi, Naoko Asahina, Norio Sakai, Eishin Oki, Akira Tamaoka, Kenji Yamada, Kazuyo Kuzume, Sanae Kawakami, Koji Sameshima, Saki Yokoshiki, Toshiyuki Isoe, Kiyotaka Nakamagoe, Kenji Watanabe
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 20, Iss, Pp-(2019)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Introduction: Fatty acid oxidation disorders (FAODs) are rare diseases caused by a defective mitochondrial fatty acid oxidation (FAO) enzyme. We recently reported that bezafibrate improved patient quality of life (QOL) based on the SF-36 questionnair
Publikováno v:
Journal of Research in Science Education. 52:115-122
Autor:
Eiichi Ishii, Jun Kuwabara, Hisamichi Tauchi, Atsushi Horiuchi, Yuji Watanabe, Sanae Kawakami, Kazuhiro Kameoka
Publikováno v:
Pediatrics International. 54:712-714
Iliopsoas abscess (IPA) is rare in children, particularly in neonates. A male neonate was born at 38 weeks of gestation with a weight of 2915 g. On day 22 after birth, his family noticed that his right thigh was swollen. Abdominal computed tomography
Autor:
Hisamichi Tauchi, Mariko Eguchi, Hidehiko Iwabuki, Eiichi Ishii, Sanae Kawakami, Minenori Eguchi-Ishimae, Kiriko Tokuda
Publikováno v:
European journal of haematology. 94(2)
Juvenile myelomonocytic leukemia (JMML) is a clonal disease arising from abnormal hematopoietic stem cells, although the involvement of lymphoid lineage differs among reported cases. Here, we present a case of JMML with a KRAS G13D mutation. The muta
Autor:
Atsushi, Horiuchi, Kazuhiro, Kameoka, Jun, Kuwabara, Yuji, Watanabe, Sanae, Kawakami, Hisamichi, Tauchi, Eiichi, Ishii
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 54(5)
Iliopsoas abscess (IPA) is rare in children, particularly in neonates. A male neonate was born at 38 weeks of gestation with a weight of 2915 g. On day 22 after birth, his family noticed that his right thigh was swollen. Abdominal computed tomography