Detalhe da pesquisa
1.
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
2.
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
3.
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
4.
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
5.
Evaluation of MLH1 variants of unclear significance.
Genes Chromosomes Cancer
; 57(7): 350-358, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29520894
6.
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
7.
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
8.
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
9.
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
10.
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
11.
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
12.
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
13.
Pathologic complete response with neoadjuvant imatinib for locally advanced pelvic GIST.
Int J Clin Oncol
; 16(3): 279-83, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20922448
14.
Palliative pelvic exenteration for patients with gynecological malignancies.
Arch Gynecol Obstet
; 283(5): 1107-12, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20563730
15.
The Development of the Study of Hereditary Cancer in South America.
Genet Mol Biol
; 39(2): 166-7, 2016 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-27223489
16.
MLH1 intronic variants mapping to + 5 position of splice donor sites lead to deleterious effects on RNA splicing.
Fam Cancer
; 19(4): 323-336, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32363481
17.
A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries.
Eur J Cancer
; 119: 112-121, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31442815
18.
Disparities in colorectal cancer mortality across Brazilian States. / Disparidades na mortalidade de câncer colorretal nos estados brasileiros.
Rev Bras Epidemiol
; 21: e180012, 2018 Aug 27.
Artigo
em Português, Inglês
| MEDLINE | ID: mdl-30156659
19.
The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.
Cancer Lett
; 245(1-2): 96-102, 2007 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-16494995
20.
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