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PUBMED FOR HANDHELDS

Journal Abstract Search


926 related items for PubMed ID: 19853744

  • 1. Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.
    Moore SW, Zaahl M.
    J Pediatr Surg; 2009 Oct; 44(10):1899-903. PubMed ID: 19853744
    [Abstract] [Full Text] [Related]

  • 2. A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2008 Feb; 43(2):325-9. PubMed ID: 18280283
    [Abstract] [Full Text] [Related]

  • 3. Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 "Janus" genetic variation.
    Moore SW, Zaahl M.
    J Pediatr Surg; 2010 Feb; 45(2):393-6. PubMed ID: 20152359
    [Abstract] [Full Text] [Related]

  • 4. Clinical and genetic correlations of familial Hirschsprung's disease.
    Moore SW, Zaahl M.
    J Pediatr Surg; 2015 Feb; 50(2):285-8. PubMed ID: 25638620
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  • 5. Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2.
    Moore SW, Appfelstaedt J, Zaahl MG.
    J Pediatr Surg; 2007 Feb; 42(2):326-32. PubMed ID: 17270543
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  • 6. Tissue specific somatic mutations and aganglionosis in Hirschsprung's disease.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2014 Feb; 49(2):258-61; discussion 261. PubMed ID: 24528961
    [Abstract] [Full Text] [Related]

  • 7. The ITGB2 immunomodulatory gene (CD18), enterocolitis, and Hirschsprung's disease.
    Moore SW, Sidler D, Zaahl MG.
    J Pediatr Surg; 2008 Aug; 43(8):1439-44. PubMed ID: 18675632
    [Abstract] [Full Text] [Related]

  • 8. RET proto-oncogene testing in infants presenting with Hirschsprung disease identifies 2 new multiple endocrine neoplasia 2A kindreds.
    Fialkowski EA, DeBenedetti MK, Moley JF, Bachrach B.
    J Pediatr Surg; 2008 Jan; 43(1):188-90. PubMed ID: 18206480
    [Abstract] [Full Text] [Related]

  • 9. Within-gene interaction between c.135 G/A genotypes and RET proto-oncogene germline mutations in HSCR families.
    Fitze G, Cramer J, Serra A, Schreiber M, Roesner D, Schackert HK.
    Eur J Pediatr Surg; 2003 Jun; 13(3):152-7. PubMed ID: 12939698
    [Abstract] [Full Text] [Related]

  • 10. Mutation analysis of endothelin-B receptor gene in patients with Hirschsprung disease in Taiwan.
    Lin YC, Lai HS, Hsu WM, Lee PI, Chen HL, Chang MH.
    J Pediatr Gastroenterol Nutr; 2008 Jan; 46(1):36-40. PubMed ID: 18162831
    [Abstract] [Full Text] [Related]

  • 11. Allele dosage-dependent penetrance of RET proto-oncogene in an Israeli-Arab inbred family segregating Hirschsprung disease.
    Basel-Vanagaite L, Pelet A, Steiner Z, Munnich A, Rozenbach Y, Shohat M, Lyonnet S.
    Eur J Hum Genet; 2007 Feb; 15(2):242-5. PubMed ID: 17091122
    [Abstract] [Full Text] [Related]

  • 12. Association of endothelin-beta receptor (EDNRB) gene variants in anorectal malformations.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2007 Jul; 42(7):1266-70. PubMed ID: 17618893
    [Abstract] [Full Text] [Related]

  • 13. Cys611Ser mutation in RET proto-oncogene in a kindred with medullary thyroid carcinoma and Hirschsprung's disease.
    Nishikawa M, Murakumo Y, Imai T, Kawai K, Nagaya M, Funahashi H, Nakao A, Takahashi M.
    Eur J Hum Genet; 2003 May; 11(5):364-8. PubMed ID: 12734540
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  • 15. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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