103 related articles for article (PubMed ID: 24070729)
1. Unifying diagnosis for adenomatous polyps, café-au-lait macules, and a brain mass?
Durno C; Pollett A; Gallinger S
Gastroenterology; 2013 Nov; 145(5):e3-4. PubMed ID: 24070729
[No Abstract] [Full Text] [Related]
2. Café-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.
Jackson CC; Holter S; Pollett A; Clendenning M; Chou S; Senter L; Ramphal R; Gallinger S; Boycott K
Pediatr Blood Cancer; 2008 Jun; 50(6):1268-70. PubMed ID: 18273873
[TBL] [Abstract][Full Text] [Related]
3. How helpful is age at colorectal cancer onset in finding hereditary nonpolyposis colorectal cancer?
Lynch PM
Clin Gastroenterol Hepatol; 2011 Jun; 9(6):458-60. PubMed ID: 21440092
[No Abstract] [Full Text] [Related]
4. Cell-free assay breakthrough for MLH1 variants.
Hofstra RM; Sijmons RH
Hum Mutat; 2010 Mar; 31(3):v. PubMed ID: 20162719
[No Abstract] [Full Text] [Related]
5. [Selection criteria for search for germ mutations in colorectal cancer hereditary nonpolyposis].
Ríos A; Rodríguez JM; Carbonel P; Parrilla P
Med Clin (Barc); 2015 Feb; 144(4):185-6. PubMed ID: 25458510
[No Abstract] [Full Text] [Related]
6. Café au lait macules and juvénile polyps.
Pacheco TR; Scatena LS; Hoffenberg EJ; Gralla J; Lee LA
Pediatr Dermatol; 2007; 24(3):E17-21. PubMed ID: 17509109
[TBL] [Abstract][Full Text] [Related]
7. Establishing a clinical and molecular diagnosis for hereditary colorectal cancer syndromes: Present tense, future perfect?
Jansen M; Menko FH; Brosens LA; Giardiello FM; Offerhaus GJ
Gastrointest Endosc; 2014 Dec; 80(6):1145-55. PubMed ID: 25434663
[No Abstract] [Full Text] [Related]
8. Constitutional Mismatch Repair Gene Defect Syndrome Presenting With Adenomatous Polyposis and Cafe au Lait Spots: A Case Report.
Sağ E; Erkut M; Saygin İ; Çebi AH; Bahadir A; Erduran E; Saruhan H; Cakir M
J Pediatr Hematol Oncol; 2020 Oct; 42(7):e689-e691. PubMed ID: 31599855
[TBL] [Abstract][Full Text] [Related]
9. [Standardized and structured histopathological evaluation of colorectal polyps: a practical checklist against the background of the new WHO classification].
Baretton GB; Tannapfel A; Schmitt W
Pathologe; 2011 Jul; 32(4):289-96. PubMed ID: 21678043
[TBL] [Abstract][Full Text] [Related]
10. Identifying Lynch syndrome.
de la Chapelle A; Palomaki G; Hampel H
Int J Cancer; 2009 Sep; 125(6):1492-3. PubMed ID: 19536819
[No Abstract] [Full Text] [Related]
11. Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?
Trimbath JD; Petersen GM; Erdman SH; Ferre M; Luce MC; Giardiello FM
Fam Cancer; 2001; 1(2):101-5. PubMed ID: 14574005
[TBL] [Abstract][Full Text] [Related]
12. Molecular screening for Lynch syndrome: from bench to bedside.
Jensen LH; Lindebjerg J; Kølvraa S; Crüger DG
J Clin Oncol; 2009 Dec; 27(34):e224; author reply e225. PubMed ID: 19858372
[No Abstract] [Full Text] [Related]
13. Evaluation and management of Lynch syndrome.
Boland CR
Clin Adv Hematol Oncol; 2007 Nov; 5(11):851,873. PubMed ID: 18185481
[No Abstract] [Full Text] [Related]
14. Advances in defective mismatch repair colon cancer.
Sargent DJ
Clin Adv Hematol Oncol; 2008 Sep; 6(9):639-41. PubMed ID: 18827786
[No Abstract] [Full Text] [Related]
15. A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots.
Whiteside D; McLeod R; Graham G; Steckley JL; Booth K; Somerville MJ; Andrew SE
Cancer Res; 2002 Jan; 62(2):359-62. PubMed ID: 11809679
[TBL] [Abstract][Full Text] [Related]
16. [Coexistence of Peutz-Jeghers' syndrome and Lynch's syndrome in the same patient].
Martínez Amate E; Carreño González R; Jorge Cerrudo J; Esteban Carretero J
Gastroenterol Hepatol; 2012; 35(6):395-9. PubMed ID: 22516349
[TBL] [Abstract][Full Text] [Related]
17. The hMSH2 and hMLH1 genes in hereditary nonpolyposis colorectal cancer.
Lynch PM
Surg Oncol Clin N Am; 2009 Oct; 18(4):611-24. PubMed ID: 19793569
[TBL] [Abstract][Full Text] [Related]
18. Decoding hereditary colorectal cancer.
Boland CR
N Engl J Med; 2006 Jun; 354(26):2815-7. PubMed ID: 16807419
[No Abstract] [Full Text] [Related]
19. Uterine carcinosarcoma associated with hereditary nonpolyposis colorectal cancer.
South SA; Hutton M; Farrell C; Mhawech-Fauceglia P; Rodabaugh KJ
Obstet Gynecol; 2007 Aug; 110(2 Pt 2):543-5. PubMed ID: 17666659
[TBL] [Abstract][Full Text] [Related]
20. [Methylation is a frequent mechanism of inactivation of the hMLH1 gene copies in sporadic colonic cancer].
Larsen CJ
Bull Cancer; 1998 Sep; 85(9):741-2. PubMed ID: 9817055
[No Abstract] [Full Text] [Related]
[Next] [New Search]
