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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

200 related articles for article (PubMed ID: 36857021)

  • 1. Comprehensive characterization of the genetic landscape of familial Hirschsprung's disease.
    Xiao J; Hao LW; Wang J; Yu XS; You JY; Li ZJ; Mao HD; Meng XY; Feng JX
    World J Pediatr; 2023 Jul; 19(7):644-651. PubMed ID: 36857021
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.
    Edery P; Pelet A; Mulligan LM; Abel L; Attié T; Dow E; Bonneau D; David A; Flintoff W; Jan D
    J Med Genet; 1994 Aug; 31(8):602-6. PubMed ID: 7815416
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung's disease.
    Ding HY; Lei W; Xiao SJ; Deng H; Yuan LK; Xu L; Zhou JL; Huang R; Fang YL; Wang QY; Zhang Y; Zhang L; Zhu XC
    Pediatr Surg Int; 2024 Jan; 40(1):38. PubMed ID: 38253735
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locus.
    de Pontual L; Pelet A; Trochet D; Jaubert F; Espinosa-Parrilla Y; Munnich A; Brunet JF; Goridis C; Feingold J; Lyonnet S; Amiel J
    J Med Genet; 2006 May; 43(5):419-23. PubMed ID: 16443855
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease.
    Dvoráková S; Dvoráková K; Malíková M; Skába R; Vlcek P; Bendlová B
    J Pediatr Surg; 2005 Jun; 40(6):e1-6. PubMed ID: 15991157
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The association between Hirschsprung's disease and multiple endocrine neoplasia type 2a: a systematic review.
    Coyle D; Friedmacher F; Puri P
    Pediatr Surg Int; 2014 Aug; 30(8):751-6. PubMed ID: 24972642
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.
    Attié T; Pelet A; Edery P; Eng C; Mulligan LM; Amiel J; Boutrand L; Beldjord C; Nihoul-Fékété C; Munnich A
    Hum Mol Genet; 1995 Aug; 4(8):1381-6. PubMed ID: 7581377
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hirschsprung's disease as a model of complex genetic etiology.
    Borrego S; Ruiz-Ferrer M; Fernández RM; Antiñolo G
    Histol Histopathol; 2013 Sep; 28(9):1117-36. PubMed ID: 23605783
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Occurrence of MEN 2a in familial Hirschsprung's disease: a new indication for genetic testing of the RET proto-oncogene.
    Decker RA; Peacock ML
    J Pediatr Surg; 1998 Feb; 33(2):207-14. PubMed ID: 9498388
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fine mapping of the 9q31 Hirschsprung's disease locus.
    Tang CS; Sribudiani Y; Miao XP; de Vries AR; Burzynski G; So MT; Leon YY; Yip BH; Osinga J; Hui KJ; Verheij JB; Cherny SS; Tam PK; Sham PC; Hofstra RM; Garcia-Barceló MM
    Hum Genet; 2010 Jun; 127(6):675-83. PubMed ID: 20361209
    [TBL] [Abstract][Full Text] [Related]  

  • 14. RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's disease.
    Pasini B; Rossi R; Ambrosio MR; Zatelli MC; Gullo M; Gobbo M; Collini P; Aiello A; Pansini G; Trasforini G; degli Uberti EC
    Surgery; 2002 Apr; 131(4):373-81. PubMed ID: 11935126
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
    Salomon R; Attié T; Pelet A; Bidaud C; Eng C; Amiel J; Sarnacki S; Goulet O; Ricour C; Nihoul-Fékété C; Munnich A; Lyonnet S
    Nat Genet; 1996 Nov; 14(3):345-7. PubMed ID: 8896569
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [From monogenic to polygenic: model of Hirschsprung disease].
    Salomon R; Amiel J; Attié T; Pelet A; Munnich A; Lyonnet S
    Pathol Biol (Paris); 1998 Nov; 46(9):705-7. PubMed ID: 9885824
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular biology, basic research and diagnosis of Hirschsprung's disease].
    Martucciello G; Luinetti O; Romano P; Magrini U
    Pathologe; 2007 Mar; 28(2):119-24. PubMed ID: 17279407
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distinctive genetic variation of long-segment Hirschsprung's disease in Taiwan.
    Yang W; Chen SC; Lai JY; Ming YC; Chen JC; Chen PL
    Neurogastroenterol Motil; 2019 Nov; 31(11):e13665. PubMed ID: 31240788
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial Hirschsprung's disease: a systematic review.
    Mc Laughlin D; Puri P
    Pediatr Surg Int; 2015 Aug; 31(8):695-700. PubMed ID: 26179259
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.