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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]