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Journal Abstract Search

214 related items for PubMed ID: 19784002

  • 21. 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; 38(4):349-51. PubMed ID: 15334515
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  • 22. [Congenital central hypoventilation syndrome, report of three cases].
    Wang Y, He XY, Yang Y, Chen XC.
    Zhonghua Er Ke Za Zhi; 2013 Nov; 51(11):852-5. PubMed ID: 24484562
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  • 23. An unusual presentation of congenital central hypoventilation syndrome (Ondine's Curse).
    Lovell BL, Bullock RE, Anderson KN.
    Emerg Med J; 2010 Mar; 27(3):237-8. PubMed ID: 20304901
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  • 27. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
    Geifman-Holtzman O, Fay K.
    Am J Med Genet; 1998 Jul 07; 78(3):250-3. PubMed ID: 9677060
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  • 28. ["Ondine's curse" in adults].
    Bullemer F, Heindl S, Karg O.
    Pneumologie; 1999 Oct 07; 53 Suppl 2():S91-2. PubMed ID: 10613051
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  • 29. 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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  • 30. Short-term blood pressure and heart rate variability in congenital central hypoventilation syndrome (Ondine's curse).
    Trang H, Girard A, Laude D, Elghozi JL.
    Clin Sci (Lond); 2005 Mar 01; 108(3):225-30. PubMed ID: 15544572
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  • 31. 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 01; 71(3):280-5. PubMed ID: 22278185
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  • 33. Haddad syndrome: a case of an infant with central congenital hypoventilation syndrome and Hirschsprung disease.
    Lai D, Schroer B.
    J Child Neurol; 2008 Mar 01; 23(3):341-3. PubMed ID: 18230845
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  • 34. Neurotrophic factor expression in three infants with Ondine's curse.
    Chiaretti A, Zorzi G, Di Rocco C, Genovese O, Antonelli A, Piastra M, Polidori G, Aloe L.
    Pediatr Neurol; 2005 Nov 01; 33(5):331-6. PubMed ID: 16243220
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  • 35. 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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  • 36. Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers.
    Jennings LJ, Yu M, Zhou L, Rand CM, Berry-Kravis EM, Weese-Mayer DE.
    Diagn Mol Pathol; 2010 Dec 15; 19(4):224-31. PubMed ID: 21051998
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  • 37. [The congenital central hypoventilation syndrome (CCHS): a late presentation].
    Lamon T, Pontier S, Têtu L, Riviere D, Didier A.
    Rev Mal Respir; 2012 Mar 15; 29(3):426-9. PubMed ID: 22440308
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  • 38. Haddad syndrome: a case study.
    Shuman L, Youmans D.
    Neonatal Netw; 2005 Mar 15; 24(4):41-4. PubMed ID: 16117243
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  • 39. 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
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  • 40. Recurrence of CCHS associated PHOX2B poly-alanine expansion mutation due to maternal mosaicism.
    Bachetti T, Di Duca M, Della Monica M, Grappone L, Scarano G, Ceccherini I.
    Pediatr Pulmonol; 2014 Mar 15; 49(3):E45-7. PubMed ID: 23460545
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