Literature DB >> 25505867

Congenital central hypoventilation syndrome with PHOX2B mutation in Saudi Arabia: a- single center experience.

Aisha Almutairi1.   

Abstract

Entities:  

Year:  2014        PMID： 25505867      PMCID： PMC4257367          DOI： 10.12816/0023984

Source DB:  PubMed          Journal:  Int J Health Sci (Qassim)        ISSN： 1658-3639


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  5 in total

1.  Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report.

Authors:  Muslim Mohammed Al Saadi
Journal:  Sleep Breath       Date:  2010-11-19       Impact factor: 2.816

2.  Failure of automatic control of ventilation (Ondine's curse). Report of an infant born with this syndrome and review of the literature.

Authors:  R B Mellins; H H Balfour; G M Turino; R W Winters
Journal:  Medicine (Baltimore)       Date:  1970-11       Impact factor: 1.889

3.  The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype.

Authors:  Ha Trang; Michel Dehan; François Beaufils; Isabelle Zaccaria; Jeanne Amiel; Claude Gaultier
Journal:  Chest       Date:  2005-01       Impact factor: 9.410

4.  An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.

Authors:  Debra E Weese-Mayer; Elizabeth M Berry-Kravis; Isabella Ceccherini; Thomas G Keens; Darius A Loghmanee; Ha Trang
Journal:  Am J Respir Crit Care Med       Date:  2010-03-15       Impact factor: 21.405

5.  Epidemiologic survey of 196 patients with congenital central hypoventilation syndrome.

Authors:  Mary Vanderlaan; Cheryl R Holbrook; Mei Wang; Andrew Tuell; David Gozal
Journal:  Pediatr Pulmonol       Date:  2004-03
  5 in total

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