These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

345 related items for PubMed ID: 26418987

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Genetic study of a patient with congenital central hypoventilation syndrome in Iran: a case report.
    Khorasanian R, Mojbafan M, Khosravi N.
    Mol Biol Rep; 2021 Dec; 48(12):8239-8243. PubMed ID: 34626313
    [Abstract] [Full Text] [Related]

  • 26. Adult cases of late-onset congenital central hypoventilation syndrome and paired-like homeobox 2B-mutation carriers: an additional case report and pooled analysis.
    Hino A, Terada J, Kasai H, Shojima H, Ohgino K, Sasaki A, Hayasaka K, Tatsumi K.
    J Clin Sleep Med; 2020 Nov 15; 16(11):1891-1900. PubMed ID: 32741443
    [Abstract] [Full Text] [Related]

  • 27. Characteristics and outcomes in children with congenital central hypoventilation syndrome on long-term mechanical ventilation in the Netherlands.
    Evers-Bikker EE, de Weerd W, Wijkstra PJ, Corel L, Verweij LP, Vosse BAH.
    Eur J Pediatr; 2024 Feb 15; 183(2):791-797. PubMed ID: 38001308
    [Abstract] [Full Text] [Related]

  • 28. A Novel c.676_677insG PHOX2B Mutation in Congenital Central Hypoventilation Syndrome.
    Ye G, Han D, Jiang Y, Wang Z, Zhou Y, Lin X, Chen W, Chen M, Xu J, Yang Y, Guo Q.
    J Clin Sleep Med; 2019 Mar 15; 15(3):509-513. PubMed ID: 30853048
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Congenital central hypoventilation syndrome: a case report.
    Crowell BA, Bissinger RL, Conway-Orgel M.
    Adv Neonatal Care; 2011 Jun 15; 11(3):167-72. PubMed ID: 21730909
    [Abstract] [Full Text] [Related]

  • 36. 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
    [Abstract] [Full Text] [Related]

  • 37. 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
    [Abstract] [Full Text] [Related]

  • 38. [Congenital central hypoventilation syndrome: paradigm shifts and future prospects].
    Hayasaka K, Sasaki A.
    Nihon Rinsho; 2014 Feb 15; 72(2):363-70. PubMed ID: 24605541
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype.
    Berry-Kravis EM, Zhou L, Rand CM, Weese-Mayer DE.
    Am J Respir Crit Care Med; 2006 Nov 15; 174(10):1139-44. PubMed ID: 16888290
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 18.