Congenital central hypoventilation syndrome mimicking mitochondrial disease-Reference-Cited by-同舟云学术

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Congenital central hypoventilation syndrome mimicking mitochondrial disease

Published:2018-01-19 Issue:3 Volume:6 Page:465-468
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Rojnueangnit Kitiwan¹²^ORCID,Descartes Maria²³

Affiliation:

1. Department of Pediatrics; Faculty of Medicine; Thammasat University; Pathumthani Thailand

2. Department of Genetics; University of Alabama at Birmingham; Birmingham Alabama

3. Department of Pediatrics; University of Alabama at Birmingham; Birmingham Alabama

Publisher

Wiley

Subject

General Medicine

Reference22 articles.

1. The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype;Trang;Chest,2005

2. Genotype-phenotype relationship in Japanese patients with congenital central hypoventilation syndrome;Shimokaze;J. Hum. Genet.,2015

3. An official ATS clinical policy statement: congenital central hypoventilation syndrome: genetic basis, diagnosis, and management;Weese-Mayer;Am. J. Respir. Crit. Care Med.,2010

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

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. HIDEA syndrome: A rare cause of congenital hypoventilation in a premature infant;Pediatric Pulmonology;2022-05-21

2. Neonatal Congenital Central Hypoventilation Syndrome: Why We Should not Sleep on it. Literature Review of Forty-two Neonatal Onset Cases;Current Pediatric Reviews;2019-12-09

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