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Journal Abstract Search

460 related items for PubMed ID: 26378991

  • 21. Carbamazepine Improves Apneic Episodes in Congenital Central Hypoventilation Syndrome (CCHS) With a Novel PHOX2B Exon 1 Missense Mutation.
    Schirwani S, Pysden K, Chetcuti P, Blyth M.
    J Clin Sleep Med; 2017 Nov 15; 13(11):1359-1362. PubMed ID: 28992836
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  • 22. Life-threatening cardiac arrhythmias in congenital central hypoventilation syndrome.
    Laifman E, Keens TG, Bar-Cohen Y, Perez IA.
    Eur J Pediatr; 2020 May 15; 179(5):821-825. PubMed ID: 31950261
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  • 27. PHOX2B mutation in a Taiwanese newborn with congenital central hypoventilation syndrome.
    Wang TC, Su YN, Lai MC.
    Pediatr Neonatol; 2014 Feb 15; 55(1):68-70. PubMed ID: 23597545
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  • 29. Congenital central hypoventilation syndrome with PHOX2B gene mutation in a Taiwanese infant.
    Chen LR, Tsao PN, Su YN, Fan PC, Chou HC, Chen CY, Chang YH, Hsieh WS.
    J Formos Med Assoc; 2007 Jan 15; 106(1):69-73. PubMed ID: 17282973
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  • 37. Three-Generation Family With Congenital Central Hypoventilation Syndrome and Novel PHOX2B Gene Non-Polyalanine Repeat Mutation.
    Kasi AS, Jurgensen TJ, Yen S, Kun SS, Keens TG, Perez IA.
    J Clin Sleep Med; 2017 Jul 15; 13(7):925-927. PubMed ID: 28633714
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  • 38. Neurocognition in Congenital Central Hypoventilation Syndrome: influence of genotype and ventilation method.
    Trang H, Bourgeois P, Cheliout-Heraut F.
    Orphanet J Rare Dis; 2020 Nov 17; 15(1):322. PubMed ID: 33203435
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