Publications by authors named "Rei Nishimura"

Claim this Profile
A
Anesthetic consideration for a patient with EEC syndrome and cardiac disease.
Masanori Tsukamoto, Maho Goto, Rei Nishimura, Takashi Hitosugi, Takeshi Yokoyama

Saudi J Anaesth· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
J
Juvenile Granulosa Cell Tumor with Elevated Peripheral Interleukin-6 Level Shows Prolonged Fever and Delayed Puberty.
Keisuke Okuno, Naohiro Yoneda, Rei Nishimura, Hitoshi Sano, Jun-Ichi Ueyama

Yonago Acta Med· September 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Increased IRS2 mRNA Expression in SGA Neonates: PCR Analysis of Insulin/IGF Signaling in Cord Blood.
Masanobu Fujimoto, Yuki Kawashima Sonoyama, Kenji Fukushima, Aya Imamoto, Fumiko Miyahara, Rei Nishimura

J Endocr Soc· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel frameshift mutation in NR3C2 leads to decreased expression of mineralocorticoid receptor: a family with renal pseudohypoaldosteronism type 1.
Yuki Kawashima Sonoyama, Toshihiro Tajima, Masanobu Fujimoto, Akiko Hasegawa, Naoki Miyahara, Rei Nishimura

Endocr J· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cholesterol ester storage disease with a novel LIPA mutation (L264P) that presented massive hepatomegaly: A case report.
Naomi Kuranobu, Jun Murakami, Ken Okamoto, Rei Nishimura, Kei Murayama

Hepatol Res· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A rare CYP 21 mutation (p.E431K) induced deactivation of CYP 21A2 and resulted in congenital adrenal hyperplasia.
Yuki Kawashima, Takeshi Usui, Masanobu Fujimoto, Naoki Miyahara, Rei Nishimura

Endocr J· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Heterozygous nonsense mutations near the C-terminal region of IGF1R in two patients with small-for-gestational-age-related short stature.
Masanobu Fujimoto, Yuki Kawashima Sonoyama, Naoki Hamajima, Takashi Hamajima, Yumiko Kumura, Rei Nishimura

Clin Endocrinol (Oxf)· December 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Familial short stature is associated with a novel dominant-negative heterozygous insulin-like growth factor 1 receptor (IGF1R) mutation.
Yuki Kawashima, Fumihiko Hakuno, Shin-ichi Okada, Tomoyuki Hotsubo, Tomoe Kinoshita, Rei Nishimura

Clin Endocrinol (Oxf)· August 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical overview of nephrogenic diabetes insipidus based on a nationwide survey in Japan.
Masanobu Fujimoto, Shin-Ichi Okada, Yuki Kawashima, Rei Nishimura, Naoki Miyahara

Yonago Acta Med· June 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Leprechaunism (Donohue syndrome): a case bearing novel compound heterozygous mutations in the insulin receptor gene.
Yuki Kawashima, Rei Nishimura, Akari Utsunomiya, Reiko Kagawa, Hiroaki Funata

Endocr J· July 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis