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 *

363 related articles for article (PubMed ID: 37828049)

  • 1. Hirschsprung disease.
    Montalva L; Cheng LS; Kapur R; Langer JC; Berrebi D; Kyrklund K; Pakarinen M; de Blaauw I; Bonnard A; Gosain A
    Nat Rev Dis Primers; 2023 Oct; 9(1):54. PubMed ID: 37828049
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease.
    de Pontual L; Pelet A; Clement-Ziza M; Trochet D; Antonarakis SE; Attie-Bitach T; Beales PL; Blouin JL; Dastot-Le Moal F; Dollfus H; Goossens M; Katsanis N; Touraine R; Feingold J; Munnich A; Lyonnet S; Amiel J
    Hum Mutat; 2007 Aug; 28(8):790-6. PubMed ID: 17397038
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transanal pull-through for Hirschsprung disease.
    Dasgupta R; Langer JC
    Semin Pediatr Surg; 2005 Feb; 14(1):64-71. PubMed ID: 15770590
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.
    Moore SW
    Pediatr Surg Int; 2012 Nov; 28(11):1045-58. PubMed ID: 23001136
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. The developmental etiology and pathogenesis of Hirschsprung disease.
    Butler Tjaden NE; Trainor PA
    Transl Res; 2013 Jul; 162(1):1-15. PubMed ID: 23528997
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Glial cell line-derived neurotrophic factor family receptors are abnormally expressed in aganglionic bowel of a subpopulation of patients with Hirschsprung's disease.
    Lui VC; Samy ET; Sham MH; Mulligan LM; Tam PK
    Lab Invest; 2002 Jun; 82(6):703-12. PubMed ID: 12065680
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Long-term functional outcomes of patients with Hirschsprung disease following pull-through.
    Gunadi ; Monica Carissa T; Stevie ; Daulay EF; Yulianda D; Iskandar K; Dwihantoro A
    BMC Pediatr; 2022 May; 22(1):246. PubMed ID: 35505310
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hirschsprung's disease: genetic and functional associations of Down's and Waardenburg syndromes.
    Moore SW; Johnson AG
    Semin Pediatr Surg; 1998 Aug; 7(3):156-61. PubMed ID: 9718653
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).
    Hofstra RM; Osinga J; Tan-Sindhunata G; Wu Y; Kamsteeg EJ; Stulp RP; van Ravenswaaij-Arts C; Majoor-Krakauer D; Angrist M; Chakravarti A; Meijers C; Buys CH
    Nat Genet; 1996 Apr; 12(4):445-7. PubMed ID: 8630503
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hirschsprung's disease in children with Mowat-Wilson syndrome.
    Coyle D; Puri P
    Pediatr Surg Int; 2015 Aug; 31(8):711-7. PubMed ID: 26156877
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Remodeling of Rectal Innervation After Pullthrough Surgery for Hirschsprung Disease: Relevance to Criteria for the Determination of Retained Transition Zone.
    Kapur RP; Arnold MA; Conces MR; Ambartsumyan L; Avansino J; Levitt M; Wood R; Mast KJ
    Pediatr Dev Pathol; 2019; 22(4):292-303. PubMed ID: 30541422
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.
    Amiel J; Attié T; Jan D; Pelet A; Edery P; Bidaud C; Lacombe D; Tam P; Simeoni J; Flori E; Nihoul-Fékété C; Munnich A; Lyonnet S
    Hum Mol Genet; 1996 Mar; 5(3):355-7. PubMed ID: 8852660
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [Syndromic Hirschsprung′s disease and its mode of inheritance].
    Zhang JR; Zhang ZB
    Zhongguo Dang Dai Er Ke Za Zhi; 2018 May; 20(5):428-432. PubMed ID: 29764583
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acquired aganglionosis: a rare occurrence following pull-through procedures for Hirschsprung's disease.
    West KW; Grosfeld JL; Rescorla FJ; Vane DW
    J Pediatr Surg; 1990 Jan; 25(1):104-8; discussion 108-9. PubMed ID: 2299533
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ultrashort-segment Hirschsprung disease in a 4-year-old female.
    Rodas A; Barillas S; Ardebol J
    J Surg Case Rep; 2020 Sep; 2020(9):rjaa320. PubMed ID: 33024529
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A De Novo novel mutation of the EDNRB gene in a Taiwanese boy with Hirschsprung disease.
    Chen WC; Chang SS; Sy ED; Tsai MC
    J Formos Med Assoc; 2006 Apr; 105(4):349-54. PubMed ID: 16618617
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Outcomes in patients with Hirschsprung disease following definitive surgery.
    Gunadi ; Karina SM; Dwihantoro A
    BMC Res Notes; 2018 Sep; 11(1):644. PubMed ID: 30180876
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 19.