Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shoko Fujinaga"'
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:
Mariko Hattori, Mahoko Furujo, Shoko Fujinaga, Toshihide Kubo, Hiroki Tsuchiya, Yuki Hyodo, Kenji Urayama, Kyohei Takahashi
Publikováno v:
Indian journal of pediatrics. 85(4)
To assess the effects of growth hormone (GH) on lipid profiles in children and whether the effect is pharmacological. The authors determined serum levels of total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), non-high-density lipopr
Autor:
Mahoko Furujo, Kyohei Takahashi, Yuki Hyodo, Shoko Fujinaga, Hiroki Tsuchiya, Kenji Urayama, Toshihide Kubo, Mariko Hattori
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 30(1)
Background:This study assessed whether non-fasting lipid markers could be substituted for fasting markers in screening for dyslipidemia, whether direct measurement of non-fasting low-density lipoprotein cholesterol [LDL-C (D)] could be substituted fo
Autor:
Shoko Fujinaga, Nobuhiko Okamoto, Junya Shimizu, Shinsuke Ninomiya, Hirosuke Morita, Tomoyuki Akiyama, Jun-ichi Takanashi, Akihito Takeuchi, Toshihide Kubo
Publikováno v:
European journal of medical genetics. 58(8)
Schinzel-Giedion syndrome is a rare congenital malformation syndrome. Recently, SETBP1 was identified as the causative gene. Herein, we present a Japanese boy with Schinzel-Giedion syndrome resulting from a novel mutation in SETBP1 in order to establ