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PUBMED FOR HANDHELDS

Journal Abstract Search

515 related items for PubMed ID: 22052119

  • 21. Residual chemosensitivity to ventilatory challenges in genotyped congenital central hypoventilation syndrome.
    Carroll MS, Patwari PP, Kenny AS, Brogadir CD, Stewart TM, Weese-Mayer DE.
    J Appl Physiol (1985); 2014 Feb 15; 116(4):439-50. PubMed ID: 24381123
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  • 24. A case of congenital central hypoventilation syndrome with a novel mutation of the PHOX2B gene presenting as central sleep apnea.
    Amimoto Y, Okada K, Nakano H, Sasaki A, Hayasaka K, Odajima H.
    J Clin Sleep Med; 2014 Mar 15; 10(3):327-9. PubMed ID: 24634632
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  • 28. Hyperthyroidism hidden by congenital central hypoventilation syndrome.
    Fox DA, Weese-Mayer DE, Wensley DF, Stewart LL.
    J Pediatr Endocrinol Metab; 2015 May 15; 28(5-6):705-8. PubMed ID: 25581741
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  • 35. Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS).
    Rand CM, Yu M, Jennings LJ, Panesar K, Berry-Kravis EM, Zhou L, Weese-Mayer DE.
    Am J Med Genet A; 2012 Sep 15; 158A(9):2297-301. PubMed ID: 22821709
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  • 36. Congenital Central Hypoventilation Syndrome: Neurocognition Already Reduced in Preschool-Aged Children.
    Charnay AJ, Antisdel-Lomaglio JE, Zelko FA, Rand CM, Le M, Gordon SC, Vitez SF, Tse JW, Brogadir CD, Nelson MN, Berry-Kravis EM, Weese-Mayer DE.
    Chest; 2016 Mar 15; 149(3):809-15. PubMed ID: 26378991
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  • 37. Late-onset congenital central hypoventilation syndrome and a rare PHOX2B gene mutation.
    Magalhães J, Madureira N, Medeiros R, Fernandes PC, Oufadem M, Amiel J, Estêvão MH, Reis MG.
    Sleep Breath; 2015 Mar 15; 19(1):55-60. PubMed ID: 24792884
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  • 38. [Ondine syndrome or central congenital hypoventilation syndrome].
    Trang H.
    Rev Prat; 2006 Jan 31; 56(2):125-8. PubMed ID: 16584036
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  • 39. Later Onset Congenital Central Hypoventilation Syndrome.
    Amos L.
    Med Clin North Am; 2024 Jan 31; 108(1):215-226. PubMed ID: 37951652
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