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Journal Abstract Search

93 related items for PubMed ID: 18714200

  • 1. 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; 64(3):226-7. PubMed ID: 18714200
    [No Abstract] [Full Text] [Related]

  • 2. Diffusion tensor imaging demonstrates brainstem and cerebellar abnormalities in congenital central hypoventilation syndrome.
    Kumar R, Macey PM, Woo MA, Alger JR, Harper RM.
    Pediatr Res; 2008 Sep; 64(3):275-80. PubMed ID: 18458651
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. 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]

  • 5. 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]

  • 6. PHOX2B mutation-confirmed congenital central hypoventilation syndrome: presentation in adulthood.
    Antic NA, Malow BA, Lange N, McEvoy RD, Olson AL, Turkington P, Windisch W, Samuels M, Stevens CA, Berry-Kravis EM, Weese-Mayer DE.
    Am J Respir Crit Care Med; 2006 Oct 15; 174(8):923-7. PubMed ID: 16873766
    [Abstract] [Full Text] [Related]

  • 7. Functional brain deficits in congenital central hypoventilation syndrome: commentary on the articles by Woo et al. on page 510 and Macey et al. on page 500.
    Gaultier C.
    Pediatr Res; 2005 Apr 15; 57(4):471-2. PubMed ID: 15718351
    [No 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 15; 29(2):152-3. PubMed ID: 19274556
    [No Abstract] [Full Text] [Related]

  • 9. 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 15; 38(4):349-51. PubMed ID: 15334515
    [Abstract] [Full Text] [Related]

  • 10. 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 15; 26(4):259-60. PubMed ID: 16570083
    [Abstract] [Full Text] [Related]

  • 11. Late onset congenital central hypoventilation syndrome after exposure to general anesthesia.
    Mahfouz AK, Rashid M, Khan MS, Reddy P.
    Can J Anaesth; 2011 Dec 15; 58(12):1105-9. PubMed ID: 21989548
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 46(8):826-8. PubMed ID: 21465679
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. 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]

  • 15. [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]

  • 16. 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]

  • 17. Late-onset hypoventilation without PHOX2B mutation or hypothalamic abnormalities.
    D'Alessandro V, Mason T, Pallone MN, Patano J, Marcus CL.
    J Clin Sleep Med; 2005 Apr 15; 1(2):169-72. PubMed ID: 17561633
    [Abstract] [Full Text] [Related]

  • 18. [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
    [No Abstract] [Full Text] [Related]

  • 19. 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 15; 44(6):521-35. PubMed ID: 19422034
    [Abstract] [Full Text] [Related]

  • 20. 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 15; 98(1):192-5. PubMed ID: 18798833
    [Abstract] [Full Text] [Related]

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