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Journal Abstract Search

101 related items for PubMed ID: 15105164

  • 1. 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
    [No Abstract] [Full Text] [Related]

  • 2. Congenital central hypoventilation syndrome and the PHOX2B gene mutation.
    Marion TL, Bradshaw WT.
    Neonatal Netw; 2011 Jul 01; 30(6):397-401. PubMed ID: 22052119
    [Abstract] [Full Text] [Related]

  • 3. Case reports of congenital central hypoventilation syndrome.
    Marsh K, Ehrhardt E.
    Neonatal Netw; 2012 Jul 01; 31(3):157-61. PubMed ID: 22564311
    [Abstract] [Full Text] [Related]

  • 4. Adult identified with congenital central hypoventilation syndrome--mutation in PHOX2b gene and late-onset CHS.
    Weese-Mayer DE, Berry-Kravis EM, Zhou L.
    Am J Respir Crit Care Med; 2005 Jan 01; 171(1):88. PubMed ID: 15615891
    [No Abstract] [Full Text] [Related]

  • 5. Sinus vein thrombosis as presenting finding in the congenital central hypoventilation syndrome: an insight on the pathophysiology of the association.
    Joseph L, Goldberg S, Shahroor S, Gomori M, Mimouni FB, Picard E.
    Pediatr Pulmonol; 2011 Aug 01; 46(8):826-8. PubMed ID: 21465679
    [Abstract] [Full Text] [Related]

  • 6. [Ondine syndrome or central congenital hypoventilation syndrome].
    Trang H.
    Rev Prat; 2006 Jan 31; 56(2):125-8. PubMed ID: 16584036
    [Abstract] [Full Text] [Related]

  • 7. Congenital central hypoventilation syndrome: a neurocristopathy with disordered respiratory control and autonomic regulation.
    Rand CM, Carroll MS, Weese-Mayer DE.
    Clin Chest Med; 2014 Sep 31; 35(3):535-45. PubMed ID: 25156769
    [Abstract] [Full Text] [Related]

  • 8. Late onset congenital central hypoventilation syndrome after exposure to general anesthesia.
    Mahfouz AK, Rashid M, Khan MS, Reddy P.
    Can J Anaesth; 2011 Dec 31; 58(12):1105-9. PubMed ID: 21989548
    [Abstract] [Full Text] [Related]

  • 9. Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report.
    Al Saadi MM.
    Sleep Breath; 2011 Dec 31; 15(4):875-8. PubMed ID: 21088916
    [No Abstract] [Full Text] [Related]

  • 10. [Ondine syndrome].
    Schenk M.
    Dtsch Med Wochenschr; 2010 Jun 31; 135(24):p24. PubMed ID: 20556722
    [No Abstract] [Full Text] [Related]

  • 11. PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome.
    Or SF, Tong MF, Lo FM, Law CW, Miu TY, Trochet D, Lam TS.
    Chin Med J (Engl); 2006 Oct 20; 119(20):1749-52. PubMed ID: 17097025
    [No Abstract] [Full Text] [Related]

  • 12. PHOX2B gene mutation in a patient with late-onset central hypoventilation.
    Trang H, Laudier B, Trochet D, Munnich A, Lyonnet S, Gaultier C, Amiel J.
    Pediatr Pulmonol; 2004 Oct 20; 38(4):349-51. PubMed ID: 15334515
    [Abstract] [Full Text] [Related]

  • 13. [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 20; 30(8):706-33. PubMed ID: 24182656
    [No Abstract] [Full Text] [Related]

  • 14. Late-onset central hypoventilation syndrome: a family genetic study.
    Doherty LS, Kiely JL, Deegan PC, Nolan G, McCabe S, Green AJ, Ennis S, McNicholas WT.
    Eur Respir J; 2007 Feb 20; 29(2):312-6. PubMed ID: 17264323
    [Abstract] [Full Text] [Related]

  • 15. 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 20; 26(4):259-60. PubMed ID: 16570083
    [Abstract] [Full Text] [Related]

  • 16. Congenital central hypoventilation syndrome: a case report.
    Crowell BA, Bissinger RL, Conway-Orgel M.
    Adv Neonatal Care; 2011 Jun 20; 11(3):167-72. PubMed ID: 21730909
    [Abstract] [Full Text] [Related]

  • 17. Pupillometry in congenital central hypoventilation syndrome (CCHS): quantitative evidence of autonomic nervous system dysregulation.
    Patwari PP, Stewart TM, Rand CM, Carroll MS, Kuntz NL, Kenny AS, Brogadir CD, Weese-Mayer DE.
    Pediatr Res; 2012 Mar 20; 71(3):280-5. PubMed ID: 22278185
    [Abstract] [Full Text] [Related]

  • 18. Unusual case of central alveolar hypoventilation. Lessons learned from ventilatory management of patients with alveolar hypoventilation in critical care conditions.
    Briones Claudett KH, Grunauer M.
    Saudi Med J; 2018 May 20; 39(5):534-535. PubMed ID: 29738021
    [Abstract] [Full Text] [Related]

  • 19. Teaching NeuroImages: alternating ptosis and Marcus Gunn jaw-winking phenomenon with PHOX2B mutation.
    Basu AP, Bellis P, Whittaker RG, McKean MC, Devlin AM.
    Neurology; 2012 Oct 23; 79(17):e153. PubMed ID: 23091080
    [No Abstract] [Full Text] [Related]

  • 20. PHOX2B in respiratory control: lessons from congenital central hypoventilation syndrome and its mouse models.
    Amiel J, Dubreuil V, Ramanantsoa N, Fortin G, Gallego J, Brunet JF, Goridis C.
    Respir Physiol Neurobiol; 2009 Aug 31; 168(1-2):125-32. PubMed ID: 19712905
    [Abstract] [Full Text] [Related]

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