153 related articles for article (PubMed ID: 28555354)
21. A cohort analysis of men with a family history of BRCA1/2 and Lynch mutations for prostate cancer.
Kerr L; Rewhorn MJ; Longmuir M; Fraser S; Walsh S; Andrew N; Leung HY
BMC Cancer; 2016 Jul; 16():529. PubMed ID: 27456091
[TBL] [Abstract][Full Text] [Related]
22. Lynch syndrome (hereditary nonpolyposis colorectal cancer) diagnostics.
Lagerstedt Robinson K; Liu T; Vandrovcova J; Halvarsson B; Clendenning M; Frebourg T; Papadopoulos N; Kinzler KW; Vogelstein B; Peltomäki P; Kolodner RD; Nilbert M; Lindblom A
J Natl Cancer Inst; 2007 Feb; 99(4):291-9. PubMed ID: 17312306
[TBL] [Abstract][Full Text] [Related]
23. Working through a diagnostic challenge: colonic polyposis, Amsterdam criteria, and a mismatch repair mutation.
Jasperson KW; Blazer KR; Lowstuter K; Weitzel JN
Fam Cancer; 2008; 7(4):281-5. PubMed ID: 18176851
[TBL] [Abstract][Full Text] [Related]
24. Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome.
Carneiro da Silva F; Ferreira JR; Torrezan GT; Figueiredo MC; Santos ÉM; Nakagawa WT; Brianese RC; Petrolini de Oliveira L; Begnani MD; Aguiar-Junior S; Rossi BM; Ferreira Fde O; Carraro DM
PLoS One; 2015; 10(10):e0139753. PubMed ID: 26437257
[TBL] [Abstract][Full Text] [Related]
25. Women with synchronous primary cancers of the endometrium and ovary: do they have Lynch syndrome?
Soliman PT; Broaddus RR; Schmeler KM; Daniels MS; Gonzalez D; Slomovitz BM; Gershenson DM; Lu KH
J Clin Oncol; 2005 Dec; 23(36):9344-50. PubMed ID: 16361634
[TBL] [Abstract][Full Text] [Related]
26. Identification of a Variety of Mutations in Cancer Predisposition Genes in Patients With Suspected Lynch Syndrome.
Yurgelun MB; Allen B; Kaldate RR; Bowles KR; Judkins T; Kaushik P; Roa BB; Wenstrup RJ; Hartman AR; Syngal S
Gastroenterology; 2015 Sep; 149(3):604-13.e20. PubMed ID: 25980754
[TBL] [Abstract][Full Text] [Related]
27. [Recognition of congenital endometrial carcinoma: the importance of family history and investigation of microsatellite instability in the tumour].
Hoogerbrugge N; Overbeek LI; de Hullu J; Kets CM; Hebeda KM; Ligtenberg MJ
Ned Tijdschr Geneeskd; 2007 Jun; 151(26):1441-4. PubMed ID: 17633970
[TBL] [Abstract][Full Text] [Related]
28. Lynch Syndrome/Hereditary Non-polyposis Colorectal Cancer (HNPCC).
Stoffel EM
Minerva Gastroenterol Dietol; 2010 Mar; 56(1):45-53. PubMed ID: 20190724
[TBL] [Abstract][Full Text] [Related]
29. Clinical implications of advances in the molecular genetics of colorectal cancer.
Lynch HT; Lynch JF
Tumori; 1995; 81(3 Suppl):19-29. PubMed ID: 7571049
[TBL] [Abstract][Full Text] [Related]
30. Mismatch repair deficiency testing in clinical practice.
Buza N; Ziai J; Hui P
Expert Rev Mol Diagn; 2016; 16(5):591-604. PubMed ID: 26895074
[TBL] [Abstract][Full Text] [Related]
31. Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
Hampel H; Frankel W; Panescu J; Lockman J; Sotamaa K; Fix D; Comeras I; La Jeunesse J; Nakagawa H; Westman JA; Prior TW; Clendenning M; Penzone P; Lombardi J; Dunn P; Cohn DE; Copeland L; Eaton L; Fowler J; Lewandowski G; Vaccarello L; Bell J; Reid G; de la Chapelle A
Cancer Res; 2006 Aug; 66(15):7810-7. PubMed ID: 16885385
[TBL] [Abstract][Full Text] [Related]
32. A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.
Liu Q; Hesson LB; Nunez AC; Packham D; Williams R; Ward RL; Sloane MA
Carcinogenesis; 2016 Jan; 37(1):10-17. PubMed ID: 26498247
[TBL] [Abstract][Full Text] [Related]
33. [Lynch Syndrome].
Akagi K
Gan To Kagaku Ryoho; 2019 Jul; 46(7):1097-1102. PubMed ID: 31296810
[TBL] [Abstract][Full Text] [Related]
34. First description of mutational analysis of MLH1, MSH2 and MSH6 in Algerian families with suspected Lynch syndrome.
Ziada-Bouchaar H; Sifi K; Filali T; Hammada T; Satta D; Abadi N
Fam Cancer; 2017 Jan; 16(1):57-66. PubMed ID: 27468915
[TBL] [Abstract][Full Text] [Related]
35. Phenotypic Heterogeneity by Germline Mismatch Repair Gene Defect in Lynch Syndrome Patients.
Hernâni-Eusébio J; Barbosa E
Acta Med Port; 2016 Oct; 29(10):587-596. PubMed ID: 28103454
[TBL] [Abstract][Full Text] [Related]
36. Identification of MSH2 inversion of exons 1-7 in clinical evaluation of families with suspected Lynch syndrome.
Mork ME; Rodriguez A; Taggart MW; Rodriguez-Bigas MA; Lynch PM; Bannon SA; You YN; Vilar E
Fam Cancer; 2017 Jul; 16(3):357-361. PubMed ID: 28004223
[TBL] [Abstract][Full Text] [Related]
37. Lynch syndrome and MYH-associated polyposis: review and testing strategy.
Goodenberger M; Lindor NM
J Clin Gastroenterol; 2011 Jul; 45(6):488-500. PubMed ID: 21325953
[TBL] [Abstract][Full Text] [Related]
38. Co-occurrence of Lynch syndrome and juvenile polyposis syndrome confirmed by multigene panel testing.
Silva-Smith R; Sussman DA
Fam Cancer; 2018 Jan; 17(1):87-90. PubMed ID: 28600700
[TBL] [Abstract][Full Text] [Related]
39. Genetic/Familial High-Risk Assessment: Colorectal Version 1.2016, NCCN Clinical Practice Guidelines in Oncology.
Provenzale D; Gupta S; Ahnen DJ; Bray T; Cannon JA; Cooper G; David DS; Early DS; Erwin D; Ford JM; Giardiello FM; Grady W; Halverson AL; Hamilton SR; Hampel H; Ismail MK; Klapman JB; Larson DW; Lazenby AJ; Lynch PM; Mayer RJ; Ness RM; Regenbogen SE; Samadder NJ; Shike M; Steinbach G; Weinberg D; Dwyer M; Darlow S
J Natl Compr Canc Netw; 2016 Aug; 14(8):1010-30. PubMed ID: 27496117
[TBL] [Abstract][Full Text] [Related]
40. Three molecular pathways model colorectal carcinogenesis in Lynch syndrome.
Ahadova A; Gallon R; Gebert J; Ballhausen A; Endris V; Kirchner M; Stenzinger A; Burn J; von Knebel Doeberitz M; Bläker H; Kloor M
Int J Cancer; 2018 Jul; 143(1):139-150. PubMed ID: 29424427
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
