An Official ATS Clinical Policy Statement: Congenital Central Hypoventilation Syndrome-Reference-Cited by-同舟云学术

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An Official ATS Clinical Policy Statement: Congenital Central Hypoventilation Syndrome

Published:2010-03-15 Issue:6 Volume:181 Page:626-644
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

Weese-Mayer Debra E.,Berry-Kravis Elizabeth M.,Ceccherini Isabella,Keens Thomas G.,Loghmanee Darius A.,Trang Ha

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference148 articles.

1. Idiopathic Congenital Central Hypoventilation Syndrome

2. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

3. Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b

4. Molecular analysis of congenital central hypoventilation syndrome

5. PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

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