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Journal Abstract Search

163 related items for PubMed ID: 17097025

  • 21. Late onset congenital central hypoventilation syndrome after exposure to general anesthesia.
    Mahfouz AK, Rashid M, Khan MS, Reddy P.
    Can J Anaesth; 2011 Dec; 58(12):1105-9. PubMed ID: 21989548
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  • 22. Congenital Central Hypoventilation syndrome (Ondine's curse): prenatal diagnosis and fetal breathing characteristics.
    Rajendran GP, Kessler MS, Manning FA.
    J Perinatol; 2009 Oct; 29(10):712-3. PubMed ID: 19784002
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  • 23. Case report of Haddad syndrome in a newborn: congenital central hypoventilation syndrome and Hirschsprung's disease.
    Dejhalla M, Parton P, Golombek SG.
    J Perinatol; 2006 Apr; 26(4):259-60. PubMed ID: 16570083
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  • 24. [Congenital central hypoventilation syndrome: analysis of PHOX2B gene mutation in a case].
    Yan Y, Yi B, Liu D, Zhao F, Zhang C, Chen X, Hao S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Oct; 32(5):665-9. PubMed ID: 26418987
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  • 25. Haddad syndrome: a case of an infant with central congenital hypoventilation syndrome and Hirschsprung disease.
    Lai D, Schroer B.
    J Child Neurol; 2008 Mar; 23(3):341-3. PubMed ID: 18230845
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  • 30. Congenital central hypoventilation syndrome.
    Ramanantsoa N, Gallego J.
    Respir Physiol Neurobiol; 2013 Nov 01; 189(2):272-9. PubMed ID: 23692929
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  • 31. In pursuit (and discovery) of a genetic basis for congenital central hypoventilation syndrome.
    Weese-Mayer DE, Berry-Kravis EM, Marazita ML.
    Respir Physiol Neurobiol; 2005 Nov 15; 149(1-3):73-82. PubMed ID: 16054879
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  • 32. Characterization of dermatoglyphics in PHOX2B-confirmed congenital central hypoventilation syndrome.
    Todd ES, Scott NM, Weese-Mayer DE, Weinberg SM, Berry-Kravis EM, Silvestri JM, Kenny AS, Hauptman SA, Zhou L, Marazita ML.
    Pediatrics; 2006 Aug 15; 118(2):e408-14. PubMed ID: 16882781
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  • 33. Structural abnormalities in the brainstem and cerebellum in congenital central hypoventilation syndrome: commentary on the article by Kumar et al. on page 275.
    Kinney HC.
    Pediatr Res; 2008 Sep 15; 64(3):226-7. PubMed ID: 18714200
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  • 34. Congenital central hypoventilation syndrome: a case report.
    Crowell BA, Bissinger RL, Conway-Orgel M.
    Adv Neonatal Care; 2011 Jun 15; 11(3):167-72. PubMed ID: 21730909
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  • 37. [ATS clinical policy statement: congenital central hypoventilation syndrome. Genetic basis, diagnosis and management].
    Weese-Mayer DE, Berry-Kravis EM, Ceccherini I, Keens TG, Loghmanee DA, Trang H, sous-commission « syndrome d’hypoventilation alvéolaire centrale congénitale » de l’American Thoracic Society.
    Rev Mal Respir; 2013 Oct 15; 30(8):706-33. PubMed ID: 24182656
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  • 38. Heterozygous 24-polyalanine repeats in the PHOX2B gene with different manifestations across three generations.
    Chuen-im P, Marwan S, Carter J, Kemp J, Rivera-Spoljaric K.
    Pediatr Pulmonol; 2014 Feb 15; 49(2):E13-6. PubMed ID: 23460419
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  • 39. Genetics of congenital central hypoventilation syndrome: lessons from a seemingly orphan disease.
    Weese-Mayer DE, Berry-Kravis EM.
    Am J Respir Crit Care Med; 2004 Jul 01; 170(1):16-21. PubMed ID: 15105164
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