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Works matching IS 09185739 AND DT 2015 AND VI 24 AND IP 3

Results: 5

1

Two Japanese patients with the renal form of pseudohypoaldosteronism type 1 caused by mutations of NR3C2.

Published in:

2015

By:

Shuntaro Morikawa;
Nagisa Komatsu;
Sonoko Sakata;
Akari Nakamura-Utsunomiya;
Satoshi Okada;
Toshihiro Tajima

Publication type:

Case Study

2

Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision).

Published in:

Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 107

By:

Keisuke Nagasaki;
Kanshi Minamitani;
Makoto Anzo;
Masanori Adachi;
Tomohiro Ishii;
Kazumichi Onigata;
Satoshi Kusuda;
Shohei Harada;
Reiko Horikawa;
Masanori Minagawa;
Haruo Mizuno;
Yuji Yamakami;
Masaru Fukushi;
Toshihiro Tajima

Publication type:

Article

3

Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision).

Published in:

Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 77

By:

Tomohiro Ishii;
Makoto Anzo;
Masanori Adachi;
Kazumichi Onigata;
Satoshi Kusuda;
Keisuke Nagasaki;
Shohei Harada;
Reiko Horikawa;
Masanori Minagawa;
Kanshi Minamitani;
Haruo Mizuno;
Yuji Yamakami;
Masaru Fukushi;
Toshihiro Tajima

Publication type:

Article

4

Single serum cortisol values at 09:00 h can be indices of adrenocortical function in children with Kawasaki disease treated with intravenous immunoglobulin plus prednisolone.

Published in:

Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 69, doi. 10.1297/cpe.24.69

By:

Masahiro Goto;
Naoyuki Miyagawa;
Kaori Kikunaga;
Masaru Miura;
Yukihiro Hasegawa

Publication type:

Article

5

A case of spondyloepiphyseal dysplasia tarda caused by a novel intragenic deletion of TRAPPC2.

Published in:

2015

By:

Masaki Takagi;
Hiroko Yagi;
Yoshie Nakamura;
Hiroyuki Shinohara;
Ryojun Takeda;
Aya Shimada;
Gen Nishimura;
Yukihiro Hasegawa

Publication type:

Case Study