E-LIB Suche - Ergebnisse für: Mizuno, Haruo

1

Genotype–Phenotype Correlations in 30 Japanese Patients Wit..:

Tanase-Nakao, Kanako ; Iwahashi-Odano, Megumi ; Sugisawa, Chiho...
The Journal of Clinical Endocrinology & Metabolism. 109 (2024) 9 - p. 2358-2365 , 2024

Link: https://doi.org/10.1210/..

2

Japanese siblings with cartilage‐hair hypoplasia exhibiting..:

Kumagai, Naonori ; Funato, Yusuke ; Wakamatsu, Manabu..
Pediatrics International. 65 (2023) 1 - p. , 2023

Link: https://doi.org/10.1111/..

3

An infant with a heterozygous variant of ABCG5presented wit..:

Yoshida, Aya ; Aoyama, Kohei ; Yamaguchi, Naoya...
Clinical Pediatric Endocrinology. 32 (2023) 2 - p. 114-118 , 2023

Link: https://doi.org/10.1297/..

4

The iodide transporter Slc26a7 impacts thyroid function mor..:

Yamaguchi, Naoya ; Suzuki, Atsushi ; Yoshida, Aya...
Scientific Reports. 12 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

5

Partial nephrogenic diabetes insipidus with a novel arginin..:

Ishida, Atsushi ; Mizuno, Haruo ; Aoyama, Kohei...
Clinical Pediatric Endocrinology. 31 (2022) 1 - p. 44-49 , 2022

Link: https://doi.org/10.1297/..

6

Regional Difference in Myelination in Monocarboxylate Trans..:

Iwayama, Hideyuki ; Tanaka, Tatsushi ; Aoyama, Kohei...
Frontiers in Neurology. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

7

Pregnancy outcome of Japanese patients with glucokinase–mat..:

Hosokawa, Yuki ; Higuchi, Shinji ; Kawakita, Rie...
Journal of Diabetes Investigation. 10 (2019) 6 - p. 1586-1589 , 2019

Link: https://doi.org/10.1111/..

8

Congenital goitrous hypothyroidism is caused by dysfunction..:

Ishii, Jun ; Suzuki, Atsushi ; Kimura, Toru...
Communications Biology. 2 (2019) 1 - p. , 2019

Link: https://doi.org/10.1038/..

9

Incidence rate and characteristics of symptomatic vitamin D..:

Kubota, Takuo ; Nakayama, Hirofumi ; Kitaoka, Taichi...
Endocrine Journal. 65 (2018) 6 - p. 593-599 , 2018

Link: https://doi.org/10.1507/..

10

Individual Clinically Diagnosed with CHARGE Syndrome but wi..:

Sakata, Sonoko ; Okada, Satoshi ; Aoyama, Kohei...
Frontiers in Genetics. 8 (2017) - p. , 2017

Link: https://doi.org/10.3389/..

11

Guidelines for diagnosis and treatment of 21-hydroxylase de..:

Mass Screening Committee, Japanese Society for Pediatric Endocrinology, and Japanese Society for Mass Screening ; Ishii, Tomohiro ; Anzo, Makoto...
Clinical Pediatric Endocrinology. 24 (2015) 3 - p. 77-105 , 2015

Link: https://doi.org/10.1297/..

12

Guidelines for Mass Screening of Congenital Hypothyroidism ..:

Mass Screening Committee, Japanese Society for Pediatric Endocrinology, and Japanese Society for Mass Screening ; Nagasaki, Keisuke ; Minamitani, Kanshi...
Clinical Pediatric Endocrinology. 24 (2015) 3 - p. 107-133 , 2015

Link: https://doi.org/10.1297/..

13

Clinical features of late-onset circulatory dysfunction in ..:

Koyama, Norihisa ; Kouwaki, Masanori ; Tanaka, Taihei...
Research and Reports in Neonatology. , 2014

Link: https://doi.org/10.2147/..

14

Functional ovarian cysts in a neonate with classical 21-hyd..:

Iwayama, Hideyuki ; Mizuno, Haruo ; Hayashi, Yutaro..
International Journal of Pediatric Endocrinology. 2013 (2013) S1 - p. , 2013

Link: https://doi.org/10.1186/..

15

Usefulness of insulin detemir in Japanese children with typ..:

Jinno, Kazuhiko ; Urakami, Tatsuhiko ; Horikawa, Reiko...
Pediatrics International. 54 (2012) 6 - p. 773-779 , 2012

Link: https://doi.org/10.1111/..