BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 38146137)

  • 21. SMAD4 juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia presenting in a middle-aged man as a large fungating gastric mass, polyposis in both upper and lower GI tract and iron deficiency anaemia, with no known family history.
    Chang W; Renaut P; Pretorius C
    BMJ Case Rep; 2020 Dec; 13(12):. PubMed ID: 33370972
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Familial juvenile polyposis syndrome with a novel SMAD4 germline mutation.
    Honda Y; Sato Y; Yokoyama J; Kobayashi M; Narisawa R; Kawauchi Y; Hoshi T; Yajima K; Kanda T; Ajioka Y; Hatakeyama K; Aoyagi Y
    Clin J Gastroenterol; 2013 Oct; 6(5):361-7. PubMed ID: 26181832
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Juvenile polyposis syndrome: a study of genotype, phenotype, and long-term outcome.
    Latchford AR; Neale K; Phillips RK; Clark SK
    Dis Colon Rectum; 2012 Oct; 55(10):1038-43. PubMed ID: 22965402
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia.
    Aagaard KS; Brusgaard K; Miceikaite I; Larsen MJ; Kjeldsen AD; Lester EB; Ousager LB; Tørring PM
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1498. PubMed ID: 33058509
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Manifestations of juvenile polyposis syndrome in SMAD4 mutation carriers of a kindred.
    Schwetz V; Uhrig S; Spuller E; Deutschmann A; Högenauer C
    Eur J Gastroenterol Hepatol; 2012 Aug; 24(8):988-94. PubMed ID: 22617360
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A case report of adult juvenile polyposis syndrome with SMAD4 pathogenic variant.
    Liu Y; Wang Z; Zhang Z; Sun Y; Zhang Y; Yang J
    Front Oncol; 2023; 13():1114097. PubMed ID: 36950548
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Gastrointestinal juvenile-like (inflammatory/hyperplastic) mucosal polyps in neurofibromatosis type 1 with no concurrent genetic or clinical evidence of other syndromes.
    Ravegnini G; Quero G; Sammarini G; Giustiniani MC; Castri F; Pomponi MG; Angelini S; Alfieri S; Genuardi M; Zamboni G; Ricci R
    Virchows Arch; 2019 Feb; 474(2):259-264. PubMed ID: 30276464
    [TBL] [Abstract][Full Text] [Related]  

  • 28. JP-HHT phenotype in Danish patients with SMAD4 mutations.
    Jelsig AM; Tørring PM; Kjeldsen AD; Qvist N; Bojesen A; Jensen UB; Andersen MK; Gerdes AM; Brusgaard K; Ousager LB
    Clin Genet; 2016 Jul; 90(1):55-62. PubMed ID: 26572829
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Gastrointestinal Bleeding in the Setting of Juvenile Polyposis Syndrome Due to SMAD4 Mutation.
    Smith PM; Tan MC
    Am Surg; 2023 Jul; 89(7):3328-3330. PubMed ID: 36809082
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genotype-defined cancer risk in juvenile polyposis syndrome.
    Aytac E; Sulu B; Heald B; O'Malley M; LaGuardia L; Remzi FH; Kalady MF; Burke CA; Church JM
    Br J Surg; 2015 Jan; 102(1):114-8. PubMed ID: 25389115
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Occurrence of gastric cancer in patients with juvenile polyposis syndrome: a systematic review and meta-analysis.
    Singh AD; Gupta A; Mehta N; Heald B; Macaron C; Liska D; Bhatt A; Burke CA
    Gastrointest Endosc; 2023 Mar; 97(3):407-414.e1. PubMed ID: 36265529
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
    Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
    Gastroenterology; 2022 Jun; 162(7):2063-2085. PubMed ID: 35487791
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
    Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
    Am J Gastroenterol; 2022 Jun; 117(6):846-864. PubMed ID: 35471415
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A novel germline SMAD4 variant detected in a Japanese family with juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia.
    Kananazawa Y; Yamada T; Yamaguchi T; Saito Y; Kakinuma D; Masuda Y; Ando F; Ohashi R; Eguchi H; Okazaki Y; Ishida H; Yoshida H
    Jpn J Clin Oncol; 2023 Mar; 53(3):275-279. PubMed ID: 36546711
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [A young man with intestinal polyposis and epistaxis].
    Menko FH; Jacobs MA; Mager JJ; Nicolaï JJ; Mensenkamp AR; Aalfs CM
    Ned Tijdschr Geneeskd; 2014; 158():A7398. PubMed ID: 25269631
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Juvenile polyposis syndrome].
    Vasovčák P; Foretová L; Puchmajerová A; Křepelová A
    Klin Onkol; 2012; 25 Suppl():S16-7. PubMed ID: 22920200
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [A case of combined syndrome of juvenile polyposis and hereditary hemorrhagic telangiectasia associated with SMAD4 mutation].
    Sumitomo Y; Yamashita Y; Itai R; Ono H; Yamada S; Matsumoto Y; Kimura Y; Ikeda E; Takada M; Mikami S
    Nihon Shokakibyo Gakkai Zasshi; 2013 Jan; 110(1):64-73. PubMed ID: 23303231
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Diagnosis and management of cancer risk in the gastrointestinal hamartomatous polyposis syndromes: recommendations from the U.S. Multi-Society Task Force on Colorectal Cancer.
    Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
    Gastrointest Endosc; 2022 Jun; 95(6):1025-1047. PubMed ID: 35487765
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Juvenile polyposis syndrome-hereditary hemorrhagic telangiectasia associated with a SMAD4 mutation in a girl.
    Hashimoto Y; Yokoyama K; Kumagai H; Okada Y; Yamagata T
    Clin J Gastroenterol; 2020 Dec; 13(6):1096-1101. PubMed ID: 32944796
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Histologic variations in juvenile polyp phenotype correlate with genetic defect underlying juvenile polyposis.
    van Hattem WA; Langeveld D; de Leng WW; Morsink FH; van Diest PJ; Iacobuzio-Donahue CA; Giardiello FM; Offerhaus GJ; Brosens LA
    Am J Surg Pathol; 2011 Apr; 35(4):530-6. PubMed ID: 21412070
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.