Congenital Adrenal Hypoplasia Due to Isolated Familial ACTH Deficiency-Reference-Cited by-同舟云学术

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Congenital Adrenal Hypoplasia Due to Isolated Familial ACTH Deficiency

Published:1994-01 Issue:2 Volume:14 Page:377-380
ISSN:0277-0938
Container-title:Pediatric Pathology
language:en
Short-container-title:Pediatric Pathology

Author:

Déchelotte P.,Darcha C.,Labbé A.,Vanlieféringhen Ph.,Beaufrére A. M.,Malpuech G.

Publisher

Informa UK Limited

Subject

Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.3109/15513819409024266

Reference11 articles.

1. A case of proved adrenocorticotropin deficiency

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature;Hormones;2019-02-12

2. Of old and new diseases: genetics of pituitary ACTH excess (Cushing) and deficiency;Clinical Genetics;2007-08-13

3. Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained byTPITGene Mutations;The Journal of Clinical Endocrinology & Metabolism;2005-03

4. Mutations du facteur de transcription Tpitet différenciation hypophysaire;médecine/sciences;2004-11

5. DAX1 and its network partners: exploring complexity in development;Molecular Genetics and Metabolism;2003-09

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