Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Erika Ogawa"'
Autor:
Sayaka Hamaguchi, Kiwako Yamamoto-Hanada, Erika Ogawa, Satoko Uematsu, Shima Ohnishi, Yushi Ito, Kenji Toyokuni, Miori Sato, Tatsuki Fukuie, Yukihiro Ohya, Ichiro Nomura
Publikováno v:
Allergology International, Vol 73, Iss 4, Pp 603-606 (2024)
Externí odkaz:
https://doaj.org/article/50a872beb0c04bab9182a6d878e2a3e3
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 38, Iss , Pp 101047- (2024)
Externí odkaz:
https://doaj.org/article/0da18bd7a8714981be77d155969d9143
Autor:
Chika Takano, Brendan H. Grubbs, Mika Ishige, Erika Ogawa, Ichiro Morioka, Satoshi Hayakawa, Toshio Miki
Publikováno v:
Stem Cells Translational Medicine, Vol 10, Iss 6, Pp 829-835 (2021)
Abstract Congenital metabolic diseases are a group of hereditary disorders caused by the deficiency of a single specific enzyme activity. Without appropriate therapy, affected patients suffer severe neurologic disability and eventual death. The curre
Externí odkaz:
https://doaj.org/article/cab063ccfdc34e078ce18ce85c921a62
Publikováno v:
Biomolecules, Vol 13, Iss 1, p 126 (2023)
Mitochondrial diabetes (MD) is generally classified as a genetic defect of β-cells. The main pathophysiology is insulin secretion failure in pancreatic β-cells due to impaired mitochondrial ATP production. However, several reports have mentioned th
Externí odkaz:
https://doaj.org/article/7bbb4d738c4340c9bd55306d2b208194
Autor:
Chika Takano, Mika Ishige, Erika Ogawa, Nobuhiko Nagano, Tamaki Morohashi, Aya Okahashi, Kaori Kawakami, Atsushi Komatsu, Kei Kawana, Tatsuhiko Urakami, Ichiro Morioka
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss , Pp 100711- (2021)
Women with congenital amino acid disorders, including maple syrup urine disease (MSUD), are at risk of metabolic crisis at delivery. There are still only a few case reports of maternal MSUD globally, and we are the first to report the successful peri
Externí odkaz:
https://doaj.org/article/800a262b23434561abe29c940d54a8e8
Autor:
Satoshi Hayakawa, Brendan H. Grubbs, Toshio Miki, Chika Takano, Mika Ishige, Ichiro Morioka, Erika Ogawa
Publikováno v:
Stem Cells Translational Medicine, Vol 10, Iss 6, Pp 829-835 (2021)
Stem Cells Translational Medicine
Stem Cells Translational Medicine
Congenital metabolic diseases are a group of hereditary disorders caused by the deficiency of a single specific enzyme activity. Without appropriate therapy, affected patients suffer severe neurologic disability and eventual death. The current mainst
Autor:
Tomoko Tsuruoka, Atsuko Imai-Okazaki, Akira Ohtake, Makiko Tajika, Minako Ogawa-Tominaga, Masaru Shimura, Taro Yamazaki, Ayako Matsunaga, Yasushi Okazaki, Erika Ogawa, Yoshihito Kishita, Takuya Fushimi, Keiko Ichimoto, Ichiro Morioka, Kei Murayama, Tatsuo Fuchigami, Masakazu Kohda, Mika Ishige
Publikováno v:
Journal of Inherited Metabolic Disease
Leigh syndrome is a major phenotype of mitochondrial diseases in children. With new therapeutic options being proposed, assessing the mortality and clinical condition of Leigh syndrome patients is crucial for evaluating therapeutics. As data are scar
Autor:
Tomohiro Morio, Kenichi Kashimada, Makoto Fujiwara, Keiichi Ozono, Kei Takasawa, Yasuki Ishihara, Takuo Kubota, Yasuhisa Ohata, Erika Ogawa, Nozomi Matsuda, Shigeru Takishima
Publikováno v:
Endocrine Journal. 67:1227-1232
Hypophosphatasia (HPP; OMIM 241510, 241500, and 146300) is an inherited metabolic disease characterized by defects of bone and tooth mineralization, which is caused by loss-of-function mutations in the ALPL gene encoding tissue non-specific alkaline
Autor:
Tatsuo Fuchigami, Maki Furukawa, Koji Hashimoto, Toshiyuki Fukao, Nobuyuki Ishige, Mika Ishige, Ryoji Fujiki, Ichiro Morioka, Yasuji Inamo, Hideo Sasai, Erika Ogawa, Hironori Kobayashi
Publikováno v:
Journal of Infection and Chemotherapy. 25:913-916
Rotavirus infection is a major cause of gastroenteritis, which occurs mainly in children. Liver dysfunction due to rotavirus gastroenteritis has been reported; however, acute hepatitis due to this disease is very rare. We present a rare case in which
Autor:
Tamaki Morohashi, Tatsuhiko Urakami, Kaori Kawakami, Atsushi Komatsu, Kei Kawana, Nobuhiko Nagano, Ichiro Morioka, Mika Ishige, Erika Ogawa, Chika Takano, Aya Okahashi
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss, Pp 100711-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Women with congenital amino acid disorders, including maple syrup urine disease (MSUD), are at risk of metabolic crisis at delivery. There are still only a few case reports of maternal MSUD globally, and we are the first to report the successful peri