Connecting you to content on EBSCOhost

Works matching IS 09185739 AND DT 2013 AND VI 22 AND IP 4

Results: 5

1

A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient with Allan-Herndon-Dudley Syndrome.

Published in:

Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 83, doi. 10.1297/cpe.22.83

By:

Yamamoto, Sayaka;
Okuhara, Koji;
Tonoki, Hidefumi;
lizuka, Susumu;
Nihei, Noriko;
Tajima, Toshihiro

Publication type:

Article

2

Brain White Matter Abnormality in a Newborn Infant with Congenital Adrenal Hyperplasia.

Published in:

Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 77, doi. 10.1297/cpe.22.77

By:

Kaga, Akimune;
Saito-Hakoda, Akiko;
Uematsu, Mitsugu;
Kamimura, Miki;
Kanno, Junko;
Kure, Shigeo;
Fujiwara, Ikuma

Publication type:

Article

3

A Case of Vitamin D Deficiency without Elevation of Serum Alkaline Phosphatase in a Carrier of Hypophosphatasia.

Published in:

Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 73, doi. 10.1297/cpe.22.73

By:

Matsuo, Kumihiro;
Mukai, Tokuo;
Furuya, Akiko;
Suzuki, Shigeru;
Tanahashi, Yusuke;
Azuma, Hiroshi

Publication type:

Article

4

Therapeutic Efficacy and Safety of GH in Japanese Children with Down Syndrome Short Stature Accompanied by GH Deficiency.

Published in:

Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 65, doi. 10.1297/cpe.22.65

By:

Meguri, Kyoko;
Inoue, Masaru;
Narahara, Koji;
Sato, Takahiro;
Takata, Ami;
Ohki, Nobuhiko;
Ozono, Keiichi

Publication type:

Article

5

Abnormal Adipose Tissue Distribution with Unfavorable Metabolic Profile in Five Children Following Hematopoietic Stem Cell Transplantation: A New Etiology for Acquired Partial Lipodystrophy.

Published in:

Clinical Pediatric Endocrinology, 2013, v. 22, n. 4, p. 53, doi. 10.1297/cpe.22.53

By:

Adachi, Masanori;
Asakura, Yumi;
Muroya, Koji;
Goto, Hiroaki;
Kigasawa, Hisato

Publication type:

Article