124 related articles for article (PubMed ID: 22180144)
1. Oncologic surveillance for subjects with biallelic mismatch repair gene mutations: 10 year follow-up of a kindred.
Durno CA; Aronson M; Tabori U; Malkin D; Gallinger S; Chan HS
Pediatr Blood Cancer; 2012 Oct; 59(4):652-6. PubMed ID: 22180144
[TBL] [Abstract][Full Text] [Related]
2. Challenges in the diagnosis and management of Lynch Syndrome in an Indigenous family living in a remote West Australian community.
Schofield L; Goldblatt J; Iacopetta B
Rural Remote Health; 2011; 11(4):1836. PubMed ID: 22188021
[TBL] [Abstract][Full Text] [Related]
3. Genetic testing in gastroenterology: Lynch syndrome.
Grover S; Syngal S
Best Pract Res Clin Gastroenterol; 2009; 23(2):185-96. PubMed ID: 19414145
[TBL] [Abstract][Full Text] [Related]
4. Microsatellite instability in saliva from patients with hereditary non-polyposis colon cancer and siblings carrying germline mismatch repair gene mutations.
Hu P; Lee CW; Xu JP; Simien C; Fan CL; Tam M; Ramagli L; Brown BW; Lynch P; Frazier ML; Siciliano MJ; Coolbaugh-Murphy M
Ann Clin Lab Sci; 2011; 41(4):321-30. PubMed ID: 22166501
[TBL] [Abstract][Full Text] [Related]
5. The gastrointestinal phenotype of germline biallelic mismatch repair gene mutations.
Durno CA; Holter S; Sherman PM; Gallinger S
Am J Gastroenterol; 2010 Nov; 105(11):2449-56. PubMed ID: 20531397
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Lynch syndrome: a pediatric perspective.
Huang SC; Durno CA; Erdman SH
J Pediatr Gastroenterol Nutr; 2014 Feb; 58(2):144-52. PubMed ID: 24051481
[TBL] [Abstract][Full Text] [Related]
8. Scoping the family history: assessment of Lynch syndrome (hereditary nonpolyposis colorectal cancer) in primary care settings--a primer for nurse practitioners.
Maradiegue A; Jasperson K; Edwards QT; Lowstuter K; Weitzel J
J Am Acad Nurse Pract; 2008 Feb; 20(2):76-84. PubMed ID: 18271762
[TBL] [Abstract][Full Text] [Related]
9. Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome.
Durno CA; Sherman PM; Aronson M; Malkin D; Hawkins C; Bakry D; Bouffet E; Gallinger S; Pollett A; Campbell B; Tabori U;
Eur J Cancer; 2015 May; 51(8):977-83. PubMed ID: 25883011
[TBL] [Abstract][Full Text] [Related]
10. Attenuated familial adenomatous polyposis and Muir-Torre syndrome linked to compound biallelic constitutional MYH gene mutations.
Ponti G; Ponz de Leon M; Maffei S; Pedroni M; Losi L; Di Gregorio C; Gismondi V; Scarselli A; Benatti P; Roncari B; Seidenari S; Pellacani G; Varotti C; Prete E; Varesco L; Roncucci L
Clin Genet; 2005 Nov; 68(5):442-7. PubMed ID: 16207212
[TBL] [Abstract][Full Text] [Related]
11. First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
Morak M; Massdorf T; Sykora H; Kerscher M; Holinski-Feder E
Eur J Cancer; 2011 May; 47(7):1046-55. PubMed ID: 21195604
[TBL] [Abstract][Full Text] [Related]
12. Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor.
Plaschke J; Linnebacher M; Kloor M; Gebert J; Cremer FW; Tinschert S; Aust DE; von Knebel Doeberitz M; Schackert HK
Eur J Hum Genet; 2006 May; 14(5):561-6. PubMed ID: 16418736
[TBL] [Abstract][Full Text] [Related]
13. Who should be sent for genetic testing in hereditary colorectal cancer syndromes?
Lynch HT; Boland CR; Rodriguez-Bigas MA; Amos C; Lynch JF; Lynch PM
J Clin Oncol; 2007 Aug; 25(23):3534-42. PubMed ID: 17687158
[TBL] [Abstract][Full Text] [Related]
14. Prediction of Lynch syndrome in consecutive patients with colorectal cancer.
Green RC; Parfrey PS; Woods MO; Younghusband HB
J Natl Cancer Inst; 2009 Mar; 101(5):331-40. PubMed ID: 19244167
[TBL] [Abstract][Full Text] [Related]
15. Colorectal adenocarcinoma: a pediatric case review with a focus on mismatch repair gene mutations and E-cadherin expression.
Gonzalez RS; Shulman SC; Katzenstein HM; Steelman CK; Wulkan ML; Abramowsky CR; Cohen C; Davis GK; Shehata BM
Pediatr Dev Pathol; 2012; 15(3):192-8. PubMed ID: 21985494
[TBL] [Abstract][Full Text] [Related]
16. [Hereditary non polyposis colorectal cancer].
Dieumegard B
Ann Med Interne (Paris); 2001 Sep; 152(5):317-21. PubMed ID: 11593143
[TBL] [Abstract][Full Text] [Related]
17. The genetics of hereditary colon cancer.
Rustgi AK
Genes Dev; 2007 Oct; 21(20):2525-38. PubMed ID: 17938238
[TBL] [Abstract][Full Text] [Related]
18. A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome.
Perera S; Ramyar L; Mitri A; Pollett A; Gallinger S; Speevak MD; Aronson M; Bapat B
J Hum Genet; 2010 Jan; 55(1):37-41. PubMed ID: 19911012
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. The Lynch syndrome: a management dilemma.
Palumbo P; Amatucci C; Perotti B; Dezzi C; Girolami M; Illuminati G; Angelici AM
Anticancer Res; 2013 May; 33(5):2147-52. PubMed ID: 23645768
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
