BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

266 related articles for article (PubMed ID: 24972642)

  • 1. 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]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET.
    Moore SW; Zaahl MG
    Pediatr Surg Int; 2008 May; 24(5):521-30. PubMed ID: 18365214
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Oncological implications of RET gene mutations in Hirschsprung's disease.
    Sijmons RH; Hofstra RM; Wijburg FA; Links TP; Zwierstra RP; Vermey A; Aronson DC; Tan-Sindhunata G; Brouwers-Smalbraak GJ; Maas SM; Buys CH
    Gut; 1998 Oct; 43(4):542-7. PubMed ID: 9824583
    [TBL] [Abstract][Full Text] [Related]  

  • 9. RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest.
    Vaclavikova E; Dvorakova S; Sykorova V; Bilek R; Dvorakova K; Vlcek P; Skaba R; Zelinka T; Bendlova B
    Endocrine; 2009 Dec; 36(3):419-24. PubMed ID: 19826964
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.
    Angrist M; Bolk S; Thiel B; Puffenberger EG; Hofstra RM; Buys CH; Cass DT; Chakravarti A
    Hum Mol Genet; 1995 May; 4(5):821-30. PubMed ID: 7633441
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biological effects of the dual phenotypic Janus mutation of ret cosegregating with both multiple endocrine neoplasia type 2 and Hirschsprung's disease.
    Arighi E; Popsueva A; Degl'Innocenti D; Borrello MG; Carniti C; Perälä NM; Pierotti MA; Sariola H
    Mol Endocrinol; 2004 Apr; 18(4):1004-17. PubMed ID: 14715928
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mechanisms of development of multiple endocrine neoplasia type 2 and Hirschsprung's disease by ret mutations.
    Takahashi M; Asai N; Iwashita T; Murakami H; Ito S
    Recent Results Cancer Res; 1998; 154():229-36. PubMed ID: 10027003
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. A MEN2A family with two asymptomatic carriers affected by unilateral renal agenesis.
    Hibi Y; Ohye T; Ogawa K; Shimizu Y; Shibata M; Kagawa C; Mizuno Y; Kurahashi H; Iwase K
    Endocr J; 2014; 61(1):19-23. PubMed ID: 24152999
    [TBL] [Abstract][Full Text] [Related]  

  • 15. C618R mutation in exon 10 of the RET proto-oncogene in a kindred with multiple endocrine neoplasia type 2A and Hirschsprung's disease.
    Caron P; Attié T; David D; Amiel J; Brousset F; Roger P; Munnich A; Lyonnet S
    J Clin Endocrinol Metab; 1996 Jul; 81(7):2731-3. PubMed ID: 8675603
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Co-segregation of MEN2 and Hirschsprung's disease: the same mutation of RET with both gain and loss-of-function?
    Takahashi M; Iwashita T; Santoro M; Lyonnet S; Lenoir GM; Billaud M
    Hum Mutat; 1999; 13(4):331-6. PubMed ID: 10220148
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Glial cell line-derived neurotrophic factor differentially stimulates ret mutants associated with the multiple endocrine neoplasia type 2 syndromes and Hirschsprung's disease.
    Carlomagno F; Melillo RM; Visconti R; Salvatore G; De Vita G; Lupoli G; Yu Y; Jing S; Vecchio G; Fusco A; Santoro M
    Endocrinology; 1998 Aug; 139(8):3613-9. PubMed ID: 9681515
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RET proto-oncogene mutations are restricted to codons 634 and 918 in mainland Chinese families with MEN2A and MEN2B.
    Zhou Y; Zhao Y; Cui B; Gu L; Zhu S; Li J; Liu J; Yin M; Zhao T; Yin Z; Yu C; Chen C; Wang L; Xiao B; Hong J; Zhang Y; Tang Z; Wang S; Li X; Ning G
    Clin Endocrinol (Oxf); 2007 Oct; 67(4):570-6. PubMed ID: 17573899
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.
    Romeo G; Ceccherini I; Celli J; Priolo M; Betsos N; Bonardi G; Seri M; Yin L; Lerone M; Jasonni V; Martucciello G
    J Intern Med; 1998 Jun; 243(6):515-20. PubMed ID: 9681852
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular analysis of the ret and GDNF genes in a family with multiple endocrine neoplasia type 2A and Hirschsprung disease.
    Borrego S; Eng C; Sánchez B; Sáez ME; Navarro E; Antiñolo G
    J Clin Endocrinol Metab; 1998 Sep; 83(9):3361-4. PubMed ID: 9745455
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.