Response to Latorraca and Palli
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://www.nature.com/articles/pr201298.pdf
Reference11 articles.
1. Latorraca NR, Palli R . A reliable prognosis for congenital central hypoventilation syndrome should reflect a patient's genetic profile and management history. Pediatr Res 2012;this issue.
2. Kumar R, Woo MS, Macey PM, Woo MA, Harper RM . Progressive gray matter changes in patients with congenital central hypoventilation syndrome. Pediatr Res 2012;71:701–6.
3. American Thoracic Society. Idiopathic congenital central hypoventilation syndrome: diagnosis and management. Am J Respir Crit Care Med 1999 160:368–73.
4. Patwari PP, Carroll MS, Rand CM, Kumar R, Harper R, Weese-Mayer DE . Congenital central hypoventilation syndrome and the PHOX2B gene: a model of respiratory and autonomic dysregulation. Respir Physiol Neurobiol 2010;173:322–35.
5. Amiel J, Laudier B, Attié-Bitach T, et al. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Nat Genet 2003;33:459–61.
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