Detalhe da pesquisa
1.
Monoallelic deleterious MUTYH germline variants as a driver for tumorigenesis.
J Pathol
; 256(2): 214-222, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34816434
2.
Dominantly inherited micro-satellite instable cancer - the four Lynch syndromes - an EHTG, PLSD position statement.
Hered Cancer Clin Pract
; 21(1): 19, 2023 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37821984
3.
Cancer risk-reducing surgery: Brazilian society of surgical oncology guideline part 1 (gynecology and breast).
J Surg Oncol
; 126(1): 10-19, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35689574
4.
Cancer risk-reducing surgery: Brazilian Society of Surgical Oncology Guideline Part 2 (Gastrointestinal and thyroid).
J Surg Oncol
; 126(1): 20-27, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35689578
5.
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium.
Hered Cancer Clin Pract
; 20(1): 36, 2022 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36182917
6.
Expanding the phenotype of E318K (c.952G > A) MITF germline mutation carriers: case series and review of the literature.
Hered Cancer Clin Pract
; 19(1): 32, 2021 Jul 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-34289891
7.
From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America.
Int J Cancer
; 145(2): 318-326, 2019 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30303536
8.
Evaluation of MLH1 variants of unclear significance.
Genes Chromosomes Cancer
; 57(7): 350-358, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29520894
9.
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
BMC Cancer
; 17(1): 623, 2017 Sep 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28874130
10.
Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes.
Int J Cancer
; 138(8): 1928-35, 2016 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26620301
11.
ROBO1 deletion as a novel germline alteration in breast and colorectal cancer patients.
Tumour Biol
; 37(3): 3145-53, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26427657
12.
A proposed staging system and stage-specific interventions for familial adenomatous polyposis.
Gastrointest Endosc
; 84(1): 115-125.e4, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26769407
13.
Angiogenesis-related protein expression in bevacizumab-treated metastatic colorectal cancer: NOTCH1 detrimental to overall survival.
BMC Cancer
; 15: 643, 2015 Sep 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26394830
14.
Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.
BMC Med Genet
; 15: 55, 2014 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24884479
15.
A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin America.
Fam Cancer
; 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38687439
16.
Mutation spectrum in South American Lynch syndrome families.
Hered Cancer Clin Pract
; 11(1): 18, 2013 Dec 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-24344984
17.
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database.
EClinicalMedicine
; 58: 101909, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37181409
18.
A novel SYBR-based duplex qPCR for the detection of gene dosage: detection of an APC large deletion in a familial adenomatous polyposis patient with an unusual phenotype.
BMC Med Genet
; 13: 55, 2012 Jul 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-22799487
19.
Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries.
BMC Cancer
; 12: 64, 2012 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22321913
20.
Breast Cancer Phenotype Associated With Li-Fraumeni Syndrome: A Brazilian Cohort Enriched by TP53 p.R337H Carriers.
Front Oncol
; 12: 836937, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35371985