Literature DB >> 9811078

Congenital central hypoventilation syndrome: an update.

D Gozal1.   

Abstract

Awareness of the existence of CCHS has led to increasingly frequent reports of such patients from all over the world. However, the exact pathophysiologic mechanisms underlying the clinical manifestations of this congenital disease entity remain unknown. For the respiratory physiologist, CCHS can be viewed as an experiment of nature that provides an important and unique window into central cardiorespiratory regulation. For the pediatrician, CCHS children represent an unique clinical challenge in coordinating the diagnostic and therapeutic procedures required to enhance the patients' quality of life.

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Year:  1998        PMID: 9811078     DOI: 10.1002/(sici)1099-0496(199810)26:4<273::aid-ppul7>3.0.co;2-c

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  24 in total

Review 1.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

2.  A whole-genome scan for 24-hour respiration rate: a major locus at 10q26 influences respiration during sleep.

Authors:  E J C de Geus; D Posthuma; N Kupper; M van den Berg; G Willemsen; A L Beem; P E Slagboom; D I Boomsma
Journal:  Am J Hum Genet       Date:  2004-11-19       Impact factor: 11.025

3.  Haddad syndrome--congenital central hypoventilation associated with Hirschsprung's disease.

Authors:  Susan D'Souza; R P Khubchandani
Journal:  Indian J Pediatr       Date:  2003-07       Impact factor: 1.967

Review 4.  Retrotrapezoid nucleus, respiratory chemosensitivity and breathing automaticity.

Authors:  Patrice G Guyenet; Douglas A Bayliss; Ruth L Stornetta; Michal G Fortuna; Stephen B G Abbott; Seth D DePuy
Journal:  Respir Physiol Neurobiol       Date:  2009-02-13       Impact factor: 1.931

5.  Airway obstruction in congenital central hypoventilation syndrome.

Authors:  Alexandra K Reverdin; Ricardo Mosquera; Giuseppe N Colasurdo; Cindy K Jon; Roya M Clements
Journal:  BMJ Case Rep       Date:  2014-05-19

6.  PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome.

Authors:  Delphine Trochet; Louise M O'Brien; David Gozal; Ha Trang; Agneta Nordenskjöld; Béatrice Laudier; Pär-Johan Svensson; Sabine Uhrig; Trevor Cole; Stephan Niemann; Arnold Munnich; Claude Gaultier; Stanislas Lyonnet; Jeanne Amiel
Journal:  Am J Hum Genet       Date:  2005-01-18       Impact factor: 11.025

Review 7.  Central respiratory chemoreception.

Authors:  Patrice G Guyenet; Ruth L Stornetta; Douglas A Bayliss
Journal:  J Comp Neurol       Date:  2010-10-01       Impact factor: 3.215

8.  A case of congenital central hypoventilation syndrome with PHOX2B gene mutation in a Korean neonate.

Authors:  Kyoung-Ah Kwon; Su-Eun Park; Shin-Yun Byun; Shine-Young Kim; Sang-Hyoun Hwang
Journal:  J Korean Med Sci       Date:  2010-07-20       Impact factor: 2.153

9.  Congenital central hypoventilation syndrome.

Authors:  P G Samdani; Vinit Samdani; Mahesh Balsekar; Akhil Goel
Journal:  Indian J Pediatr       Date:  2007-10       Impact factor: 1.967

Review 10.  The 2008 Carl Ludwig Lecture: retrotrapezoid nucleus, CO2 homeostasis, and breathing automaticity.

Authors:  Patrice G Guyenet
Journal:  J Appl Physiol (1985)       Date:  2008-06-05
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