Congenital Central Hypoventilation Syndrome-Reference-Cited by-同舟云学术

Congenital Central Hypoventilation Syndrome

Published:2016-03 Issue:3 Volume:149 Page:809-815
ISSN:0012-3692
Container-title:Chest
language:en
Short-container-title:Chest

Author:

Charnay Aaron J.,Antisdel-Lomaglio Jeanne E.,Zelko Frank A.,Rand Casey M.,Le Michele,Gordon Samantha C.,Vitez Sally F.,Tse Jennifer W.,Brogadir Cindy D.,Nelson Michael N.,Berry-Kravis Elizabeth M.,Weese-Mayer Debra E.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Reference25 articles.

1. Failure of automatic control of ventilation (Ondine's curse). Report of an infant born with this syndrome and review of the literature;Mellins;Medicine,1970

2. Idiopathic congenital central hypoventilation syndrome: diagnosis and management;Weese-Mayer;Am J Resp Crit Care,1999

3. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat Genet,2003

4. Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2B;Weese-Mayer;Am J Med Genet A,2003

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;Matera;J Med Genet,2004

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