Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Yousuke Higuchi"'
Publikováno v:
Pediatrics and Neonatology, Vol 64, Iss 5, Pp 505-511 (2023)
Background: Although the etiology of Kawasaki disease (KD) remains unknown, the most common view is that an infectious agent triggers the activation of the inflammatory cascade in predisposed children. The coronavirus disease 2019 (COVID-19) pandemic
Externí odkaz:
https://doaj.org/article/60e9b156ad47485c82a8482e43622efb
Autor:
Yousuke Higuchi, Kosei Hasegawa, Natsuko Futagawa, Miho Yamashita, Hiroyuki Tanaka, Hirokazu Tsukahara
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Abstract Background Osteogenesis imperfecta (OI) is a rare connective‐tissue disorder characterized by bone fragility. Approximately 90% of all OI cases are caused by variants in COL1A1 or COL1A2. Additionally, IFITM5 variants are responsible for t
Externí odkaz:
https://doaj.org/article/873d4c1dec394a3ea8bdfb0371df8feb
Publikováno v:
Pediatrics and Neonatology, Vol 62, Iss 5, Pp 563-564 (2021)
Externí odkaz:
https://doaj.org/article/405b3dccbd1c45f98c45b32b0b52d43f
Autor:
Yousuke Higuchi, Takayuki Motoki, Hisashi Ishida, Kiichiro Kanamitsu, Kana Washio, Takanori Oyama, Takuo Noda, Yasuko Tsurumaru, Ayumi Okada, Hirokazu Tsukahara, Akira Shimada
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-5 (2017)
Abstract Background Pediatric papillary thyroid carcinoma frequently presents with lymph node involvement and distant metastases. Sorafenib, an oral multikinase inhibitor, has been used to treat radioactive iodine (RAI) therapy-refractory thyroid car
Externí odkaz:
https://doaj.org/article/0ae03d31d0d249ecb8d311f161b25f80
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-6 (2017)
Abstract Background Stickler syndrome is a group of collagenopathies characterized by ophthalmic, skeletal, and orofacial abnormalities, with the degree of symptoms varying among patients. Mutations in the COL2A1, COL11A1, and COL11A2 procollagen gen
Externí odkaz:
https://doaj.org/article/bb613891d1b64148af81f3842d530f43
Autor:
Yousuke Higuchi1,2, Kosei Hasegawa3 haseyan@md.okayama-u.ac.jp, Toshihide Kubo2, Hiroyuki Tanaka4, Hirokazu Tsukahara1
Publikováno v:
Clinical Pediatric Endocrinology. 2022, Vol. 31 Issue 1, p38-43. 6p.
Autor:
Hiroyuki Miyahara, Kosei Hasegawa, Natsuko Futagawa, Yousuke Higuchi, Hirokazu Tsukahara, Hiroyuki Tanaka
Publikováno v:
American Journal of Medical Genetics Part A. 188:249-252
Pathogenic-activating variants of interferon induced with Helicase C domain 1 (IFIH1) cause Singleton-Merten (S-M) syndrome, which accompanies acro-osteolysis, loss of permanent teeth, and aortic calcification, as well as causing Aicardi-Goutieres (A
Autor:
Mahoko Furujo, Motoharu Ochi, Yousuke Higuchi, Takahiro Namba, Yuki Ebuchi, Hiroki Tsuchiya, Shoko Fujinaga, Naoko Urata, Toshihide Kubo, Michiko Kishi, Narumi Hara
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 33:1417-1423
Background The relationship between growth hormone (GH)-replacement therapy and the thyroid axis in GH-deficient (GHD) children remains controversial. Furthermore, there have been few reports regarding non-GHD children. We aimed to determine the effe
Autor:
Shintaro Fujiwara, Yousuke Higuchi, Yuki Ebuchi, Yu Fukushima, Takahiro Ohkura, Mahoko Furujo
Publikováno v:
Journal of Paediatrics and Child Health. 59:590-591
Autor:
Miho Yamashita, Natsuko Futagawa, Yousuke Higuchi, Kosei Hasegawa, Hirokazu Tsukahara, Hiroyuki Tanaka
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Background Osteogenesis imperfecta (OI) is a rare connective‐tissue disorder characterized by bone fragility. Approximately 90% of all OI cases are caused by variants in COL1A1 or COL1A2. Additionally, IFITM5 variants are responsible for the unique