Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Yutaka Saikawa"'
Autor:
Chiaki Shibayama, M.D., Mariko Doai, M.D.,Ph.D., Munetaka Matoba, M.D.,Ph.D., Mari Morikawa, M.D., Hitoshi Sato, M.D.,Ph.D., Naoki Okada, M.D., Yutaka Saikawa, M.D.,Ph.D., Akira Tamase, M.D.,Ph.D., Hideaki Iizuka, M.D.,Ph.D., Akihiro Shioya, M.D.,Ph.D., Sohsuke Yamada, M.D.,Ph.D.
Publikováno v:
Radiology Case Reports, Vol 16, Iss 12, Pp 3982-3986 (2021)
Externí odkaz:
https://doaj.org/article/2f95a149d0af4078bae283ecab286c33
Publikováno v:
Bone Reports, Vol 16, Iss , Pp 101569- (2022)
Pseudohypoparathyroidism type 1a (PHP1a) is a genetic disorder caused by heterozygous loss-of-function mutations on the maternal allele of the GNAS gene. Patients with PHP1a predominantly exhibit parathyroid hormone (PTH) resistance and physical feat
Externí odkaz:
https://doaj.org/article/2e60615b3bc44c17a3cab46e56abf080
Publikováno v:
Cells, Vol 12, Iss 5, p 741 (2023)
The developmental origins of health and disease (DOHaD) indicate that fetal tissues and organs in critical and sensitive periods of development are susceptible to structural and functional changes due to the adverse environment in utero. Maternal imm
Externí odkaz:
https://doaj.org/article/f0ec7029bd964177941d672955c0d3d3
Autor:
Munetaka Matoba, Mari Morikawa, Hideaki Iizuka, Mariko Doai, Hitoshi Sato, Akira Tamase, Chiaki Shibayama, Sohsuke Yamada, Yutaka Saikawa, Akihiro Shioya, Naoki Okada
Publikováno v:
Radiology Case Reports
Radiology Case Reports, Vol 16, Iss 12, Pp 3982-3986 (2021)
Radiology Case Reports, Vol 16, Iss 12, Pp 3982-3986 (2021)
Autor:
Daisuke Sakai, Yo Shimizu, Yutaka Saikawa, Toshihisa Hatta, Tsuyoshi Tsukada, Hiroki Shoji, Hiromi Sakata-Haga
Publikováno v:
Journal of Inflammation Research
Yo Shimizu,1 Tsuyoshi Tsukada,2 Hiromi Sakata-Haga,2 Daisuke Sakai,3 Hiroki Shoji,3 Yutaka Saikawa,1 Toshihisa Hatta2 1Department of Pediatrics, Kanazawa Medical University, Uchinada, Ishikawa, Japan; 2Department of Anatomy, Kanazawa Medical Universi
Autor:
Masatsune Itoh1 p-itou@kanazawa-med.ac.jp, Yutaka Saikawa1
Publikováno v:
Clinical Pediatric Endocrinology. Jan2017, Vol. 26 Issue 1, p25-28. 4p. 2 Diagrams.
Autor:
Yutaka Saikawa, Masatsune Itoh
Publikováno v:
Clinical Pediatric Endocrinology. 26:25-28
Autor:
Osamu Komiyama, Hisao Yoshida, Noriko Onishi, Masataka Ishimura, Shouichi Ohga, Chie Kobayashi, Eiji Ota, Hiroko Kozan, Yachiyo Kurihara, Ryo Niiya, Toshio Heike, Ryo Kadoya, Toshiro Hara, Tomohiro Katsuta, Toshihiko Mori, Yoshiyuki Yamada, Tomoko Waragai, Takashi Ishige, Takahiro Yasumi, Takahiro Uehara, Hiroyuki Toda, Akira Hayakawa, Satoru Kumaki, Yutaka Suzuki, Masumi Seto, Kanako Kudo, Masako Kikuchi, Hisanori Nishio, Takayuki Hoshina, Takuya Hara, Yumi Mizuno, Hidetoshi Takada, Noriko Ohbuchi, Tomoyuki Imagawa, Hiroyuki Shimizu, Maiko Igarashi, Etsuro Nanishi, Yuko Ishizaki, Masayoshi Nagao, Yutaka Saikawa, Shuhei Yajima, Yoshio Kusumoto, Shunji Hasegawa, Tomoko Sato, Hideo Tsuda, Takuro Ohno, Shohei Ogata, Yoji Sasahara, Kyouko Suzuki, Toshihiko Shirakawa
Publikováno v:
Journal of Infection. 73:358-368
Summary Objectives Patients with primary immunodeficiency diseases (PID) are highly susceptible to various microorganisms. However, no population-based studies have been performed among common viral pathogens, such as respiratory syncytial virus (RSV
Publikováno v:
Modern Rheumatology. 28:1058-1062
We report three patients with non-bacterial osteitis (NBO) who had fever of unknown origin (FUO) as an initial symptom. 18-Fluoro-2-deoxyglucose positron emission tomography (18F-FDG-PET) can be used to detect acute inflammatory lesions. There seems
Publikováno v:
Clinical Pediatric Endocrinology. 25:115-118
Tricho-rhino-phalangeal syndrome (TRPS) is a heritable congenital syndrome characterized by craniofacial and skeletal abnormalities. TRPS is an autosomal dominant syndrome with high penetrance and wide phenotypic variability. TRPS is classified into