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Journal Abstract Search

214 related items for PubMed ID: 19784002

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).
    Trochet D, de Pontual L, Estêvao MH, Mathieu Y, Munnich A, Feingold J, Goridis C, Lyonnet S, Amiel J.
    Hum Mutat; 2008 May; 29(5):770. PubMed ID: 18407552
    [Abstract] [Full Text] [Related]

  • 3. PHOX2B mutation in a Taiwanese newborn with congenital central hypoventilation syndrome.
    Wang TC, Su YN, Lai MC.
    Pediatr Neonatol; 2014 Feb; 55(1):68-70. PubMed ID: 23597545
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 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 31; 46(8):826-8. PubMed ID: 21465679
    [Abstract] [Full Text] [Related]

  • 6. Congenital central hypoventilation syndrome and the PHOX2B gene mutation.
    Marion TL, Bradshaw WT.
    Neonatal Netw; 2011 Aug 31; 30(6):397-401. PubMed ID: 22052119
    [Abstract] [Full Text] [Related]

  • 7. Congenital central hypoventilation syndrome: a case report.
    Crowell BA, Bissinger RL, Conway-Orgel M.
    Adv Neonatal Care; 2011 Jun 31; 11(3):167-72. PubMed ID: 21730909
    [Abstract] [Full Text] [Related]

  • 8. Congenital central hypoventilation syndrome (CCHS) with Hirschsprung disease (Haddad syndrome): an unusual cause of reduced baseline variability of the fetal heart rate.
    Majumdar S, Wood P.
    J Obstet Gynaecol; 2009 Feb 31; 29(2):152-3. PubMed ID: 19274556
    [No Abstract] [Full Text] [Related]

  • 9. Cardiovascular abnormalities and arrhythmias in patients with Ondine's curse (congenital central hypoventilation) syndrome.
    Movahed MR, Jalili M, Kiciman N.
    Pacing Clin Electrophysiol; 2005 Nov 31; 28(11):1226-30. PubMed ID: 16359292
    [Abstract] [Full Text] [Related]

  • 10. Congenital central hypoventilation syndrome with hirschsprung's disease due to PHOX2B gene mutation in a Turkish infant.
    Kaymakçi A, Narter F, Yazar AS, Yilmaz MS.
    Turk J Pediatr; 2012 Nov 31; 54(5):519-22. PubMed ID: 23427517
    [Abstract] [Full Text] [Related]

  • 11. Peculiar respiratory response observed during sleep-onset REM sleep of an infant with Ondine's curse.
    Takahashi R, Kakizawa H, Itou T, Yamada M, Nakae S.
    Neuropediatrics; 2000 Oct 31; 31(5):269-72. PubMed ID: 11204285
    [Abstract] [Full Text] [Related]

  • 12. 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 31; 26(4):259-60. PubMed ID: 16570083
    [Abstract] [Full Text] [Related]

  • 13. [Otoneurological findings in a case of congenital central hypoventilation syndrome (Ondine's curse)].
    Gallina S, Restivo S, Cupido G, Speciale R, Giammanco AM, Cimino G.
    Acta Otorhinolaryngol Ital; 2000 Apr 31; 20(2):121-4. PubMed ID: 10992604
    [Abstract] [Full Text] [Related]

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

  • 15. Later-onset congenital central hypoventilation syndrome due to a heterozygous 24-polyalanine repeat expansion mutation in the PHOX2B gene.
    Repetto GM, Corrales RJ, Abara SG, Zhou L, Berry-Kravis EM, Rand CM, Weese-Mayer DE.
    Acta Paediatr; 2009 Jan 31; 98(1):192-5. PubMed ID: 18798833
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse).
    de Pontual L, Népote V, Attié-Bitach T, Al Halabiah H, Trang H, Elghouzzi V, Levacher B, Benihoud K, Augé J, Faure C, Laudier B, Vekemans M, Munnich A, Perricaudet M, Guillemot F, Gaultier C, Lyonnet S, Simonneau M, Amiel J.
    Hum Mol Genet; 2003 Dec 01; 12(23):3173-80. PubMed ID: 14532329
    [Abstract] [Full Text] [Related]

  • 18. Congenital central hypoventilation syndrome from past to future: model for translational and transitional autonomic medicine.
    Weese-Mayer DE, Rand CM, Berry-Kravis EM, Jennings LJ, Loghmanee DA, Patwari PP, Ceccherini I.
    Pediatr Pulmonol; 2009 Jun 01; 44(6):521-35. PubMed ID: 19422034
    [Abstract] [Full Text] [Related]

  • 19. [Central sleep apnea (Ondine's curse syndrome) in medullary infarction].
    Planjar-Prvan M, Krmpotić P, Jergović I, Bielen I.
    Acta Med Croatica; 2010 Oct 01; 64(4):297-301. PubMed ID: 21688613
    [Abstract] [Full Text] [Related]

  • 20. [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]

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