Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Tadashi Nagata"'
Autor:
Kenichi Mishima, Atsushi Fujita, Seiji Mizuno, Masaki Matsushita, Tadashi Nagata, Yasunari Kamiya, Noriko Miyake, Naomichi Matsumoto, Shiro Imagama, Hiroshi Kitoh
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 3109-3114 (2020)
Abstract This article reports a girl with Bardet‐Biedl syndrome (BBS) having a novel causative mutation who developed Legg‐Calvé‐Perthes disease (LCPD). There exists a possibility that the prognosis of LCPD had been adversely affected by the c
Externí odkaz:
https://doaj.org/article/c903355b8ee74bb685bdffe65ba9f109
Autor:
Tadashi Nagata, Masaki Matsushita, Kenichi Mishima, Yasunari Kamiya, Kohji Kato, Miho Toyama, Tomoo Ogi, Naoki Ishiguro, Hiroshi Kitoh
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Achondroplasia (ACH), the most common form of short‐limbed skeletal dysplasia, is caused by gain‐of‐function mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. More than 97% of patients result from a heterozy
Externí odkaz:
https://doaj.org/article/6c57499fa41845d598302f1439131a92
Autor:
Hiroshi Kitoh, Masaki Matsushita, Kenichi Mishima, Tadashi Nagata, Yasunari Kamiya, Kohei Ueda, Yachiyo Kuwatsuka, Hiroshi Morikawa, Yasuhiro Nakai, Naoki Ishiguro
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0229639 (2020)
Achondroplasia (ACH) is the most common short-limbed skeletal dysplasia caused by activating mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. We identified that meclizine hydrochloride inhibited FGFR3 signaling in various chondrocyt
Externí odkaz:
https://doaj.org/article/dfebcf488aa544068e1bb6e42e213aed
Autor:
Kenichi Mishima, Hiroshi Kitoh, Masaki Matsushita, Tadashi Nagata, Yasunari Kamiya, Naoki Ishiguro
Publikováno v:
Case Reports in Orthopedics, Vol 2018 (2018)
Localized scleroderma, also known as morphea, is a rare condition characterized by progressive sclerosis of the skin and associated atrophy of the underlying tissues. The linear type of localized scleroderma is the most frequent form in childhood, us
Externí odkaz:
https://doaj.org/article/a3ca27954c4d48dca79cf4762d100dac
Autor:
Kenichi Mishima, Shiro Imagama, Tadashi Nagata, Masaki Matsushita, Hiroshi Kitoh, Yasunari Kamiya
Publikováno v:
Clinical Pediatric Endocrinology
Hypophosphatasia (HPP) is a rare skeletal dysplasia characterized by impaired bone mineralization, caused by loss-of-function mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene. Enzyme replacement therapy (ERT) by administration o
Autor:
Atsushi Fujita, Masaki Matsushita, Shiro Imagama, Noriko Miyake, Tadashi Nagata, Hiroshi Kitoh, Yasunari Kamiya, Seiji Mizuno, Kenichi Mishima, Naomichi Matsumoto
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 12, Pp 3109-3114 (2020)
Clinical Case Reports, Vol 8, Iss 12, Pp 3109-3114 (2020)
This article reports a girl with Bardet‐Biedl syndrome (BBS) having a novel causative mutation who developed Legg‐Calvé‐Perthes disease (LCPD). There exists a possibility that the prognosis of LCPD had been adversely affected by the concomitan
Autor:
Tadashi Hattori, Hiroshi Kaneko, Masaki Matsushita, Kenichi Mishima, Hiroshi Kitoh, Yasunari Kamiya, Naoki Ishiguro, Tadashi Nagata
Publikováno v:
J Clin Orthop Trauma
Purpose A multiaxial correction (MAC) fixator is a monolateral type of fixator that can correct multi-planer deformities. The purpose of this study is to compare the clinical outcome of correction for tibial deformities with the MAC fixator and the c
Autor:
Kenichi Mishima, Tadashi Nagata, Hiroshi Kitoh, Yasunari Kamiya, Tomoo Ogi, Masaki Matsushita, Naoki Ishiguro, Kohji Kato, Miho Toyama
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Background Achondroplasia (ACH), the most common form of short‐limbed skeletal dysplasia, is caused by gain‐of‐function mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. More than 97% of patients result from a heterozygous p.G3
Autor:
Naoki Ishiguro, Hiroshi Morikawa, Tadashi Nagata, Kohei Ueda, Kenichi Mishima, Hiroshi Kitoh, Yasunari Kamiya, Yachiyo Kuwatsuka, Yasuhiro Nakai, Masaki Matsushita
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0229639 (2020)
PLoS ONE
PLoS ONE
Achondroplasia (ACH) is the most common short-limbed skeletal dysplasia caused by activating mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. We identified that meclizine hydrochloride inhibited FGFR3 signaling in various chondrocyt
Autor:
Hiroshi Kitoh, Yasunari Kamiya, Masaki Matsushita, Tadashi Nagata, Naoki Ishiguro, Kenichi Mishima
Publikováno v:
Case Reports in Orthopedics, Vol 2018 (2018)
Case Reports in Orthopedics
Case Reports in Orthopedics
Localized scleroderma, also known as morphea, is a rare condition characterized by progressive sclerosis of the skin and associated atrophy of the underlying tissues. The linear type of localized scleroderma is the most frequent form in childhood, us