Detalhe da pesquisa
1.
Differences in neuropsychological and behavioral parameters and brain structure in patients with familial adenomatous polyposis: a sibling-paired study.
Hered Cancer Clin Pract
; 14: 20, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-27777639
2.
Selective Versus Universal Screening for Lynch Syndrome: A Six-Year Clinical Experience.
Dig Dis Sci
; 60(8): 2463-9, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24903654
3.
Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome.
Cancer
; 119(1): 215-25, 2013 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22786716
4.
Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome.
Gynecol Oncol
; 127(3): 544-51, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22940489
5.
Performance of Lynch syndrome predictive models in a multi-center US referral population.
Am J Gastroenterol
; 106(10): 1822-7; quiz 1828, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21747416
6.
Prevalence and predictors of appropriate colorectal cancer surveillance in Lynch syndrome.
Am J Gastroenterol
; 105(8): 1851-60, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20354509
7.
Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome.
N Engl J Med
; 354(3): 261-9, 2006 Jan 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-16421367
8.
Sharing genetic test results in Lynch syndrome: communication with close and distant relatives.
Clin Gastroenterol Hepatol
; 6(3): 333-8, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18258490
9.
Tumor histology helps to identify Lynch syndrome among colorectal cancer patients.
Fam Cancer
; 7(3): 267-74, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18283560
10.
Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study.
Clin Cancer Res
; 12(11 Pt 1): 3389-93, 2006 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-16740762
11.
Haploinsufficiency in tumor predisposition syndromes: altered genomic transcription in morphologically normal cells heterozygous for VHL or TSC mutation.
Oncotarget
; 8(11): 17628-17642, 2017 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-27682873
12.
Awareness of gynecologic surveillance in women from hereditary non-polyposis colorectal cancer families.
Fam Cancer
; 5(4): 405-9, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16937235
13.
A comparison of the phenotype and genotype in adenomatous polyposis patients with and without a family history.
Fam Cancer
; 4(2): 127-33, 2005.
Artigo
em Inglês
| MEDLINE | ID: mdl-15951963
14.
Gynecologic cancer as a "sentinel cancer" for women with hereditary nonpolyposis colorectal cancer syndrome.
Obstet Gynecol
; 105(3): 569-74, 2005 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-15738026
15.
Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X.
JAMA
; 293(16): 1979-85, 2005 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-15855431
16.
Genotype and phenotype of patients with both familial adenomatous polyposis and thyroid carcinoma.
Fam Cancer
; 2(2): 95-9, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-14574158
17.
Prospective multicenter randomized intermediate biomarker study of oral contraceptive versus depo-provera for prevention of endometrial cancer in women with Lynch syndrome.
Cancer Prev Res (Phila)
; 6(8): 774-81, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23639481
18.
APC +/- alters colonic fibroblast proteome in FAP.
Oncotarget
; 2(3): 197-208, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21411865
19.
Colorectal cancer risk perception on the basis of genetic test results in individuals at risk for Lynch syndrome.
J Clin Oncol
; 27(24): 3981-6, 2009 Aug 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-19620492
20.
One-hit effects in cancer: altered proteome of morphologically normal colon crypts in familial adenomatous polyposis.
Cancer Res
; 68(18): 7579-86, 2008 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-18794146