Intermittent Hyperglycemia due to Autonomic Nervous System Dysfunction: A New Feature in Patients with Congenital Central Hypoventilation Syndrome
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference27 articles.
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2. An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management;Weese-Mayer;Am J Respir Crit Care Med,2010
3. The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype;Trang;Chest,2005
4. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat Genet,2003
5. Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype;Berry-Kravis;Am J Respir Crit Care Med,2006
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