ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison-Reference-Cited by-同舟云学术

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ROHHAD and Prader-Willi syndrome (PWS): clinical and genetic comparison

Published:2018-07-20 Issue:1 Volume:13 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Barclay Sarah F.^ORCID,Rand Casey M.,Nguyen Lisa,Wilson Richard J. A.,Wevrick Rachel,Gibson William T.,Bech-Hansen N. Torben,Weese-Mayer Debra E.

Funder

Canadian Institutes of Health Research

Alberta Innovates - Health Solutions

BC Children’s Hospital Foundation

ROHHAD Fight Inc.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-018-0860-0.pdf

Reference39 articles.

1. Ize-Ludlow D, Gray JA, Sperling MA, Berry-Kravis EM, Milunsky JM, Farooqi IS, Rand CM, Weese-Mayer DE. Rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation presenting in childhood. Pediatrics. 2007;120(1):e179–88.

2. Fishman LS, Samson JH, Sperling DR. Primary alveolar hypoventilation syndrome (Ondine’s curse). Am J Dis Child. 1965;110:155–61.

3. Katz ES, McGrath S, Marcus CL. Late-onset central hypoventilation with hypothalamic dysfunction: a distinct clinical syndrome. Pediatr Pulmonol. 2000;29(1):62–8.

4. Bougneres P, Pantalone L, Linglart A, Rothenbuhler A, Le Stunff C. Endocrine manifestations of the rapid-onset obesity with hypoventilation, hypothalamic, autonomic dysregulation, and neural tumor syndrome in childhood. J Clin Endocrinol Metab. 2008;93(10):3971–80.

5. De Pontual L, Trochet D, Caillat-Zucman S, Abou Shenab OA, Bougneres P, Crow Y, Cunningham S, Esteva B, Heberle LC, Leger J, et al. Delineation of late onset hypoventilation associated with hypothalamic dysfunction syndrome. Pediatr Res. 2008;64(6):689–94.

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