Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience-Reference-Cited by-同舟云学术

Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience

Published:2015 Issue:1 Volume:20 Page:27
ISSN:2287-1012
Container-title:Annals of Pediatric Endocrinology & Metabolism
language:en
Short-container-title:Ann Pediatr Endocrinol Metab

Author:

Shin Sun-Jeong¹,Sul Yeonah¹,Kim Ja Hye¹,Cho Ja Hyang¹,Kim Gu-Hwan²,Kim Jae Hyun³,Choi Jin-Ho¹,Yoo Han-Wook¹

Affiliation:

1. Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

2. Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

3. Department of Pediatrics, Inje University Ilsan Paik Hospital, Goyang, Korea.

Publisher

Korean Society of Pediatric Endocrinology

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health

Link

http://e-apem.org/upload/pdf/apem-20-27.pdf

Reference40 articles.

1. The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism

2. Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

3. Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

4. Developmental aspect of the gonadotropin-releasing hormone system

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