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JCO Global Oncology|May 20, 2026
Cancer Spectrum and Gene-Specific Patterns in Lynch Syndrome: Insights From 47 Families in a Brazilian Institutional CohortThiago Bassaneze, Fábio Oliveira Ferreira, Renata Lazari Sandoval, et al.
Hereditary Cancer in Clinical Practice|July 22, 2021
Expanding the phenotype of E318K (c.952G > A) MITF germline mutation carriers: case series and review of the literatureLeandro Jonata Carvalho Oliveira, Aline Bobato Lara Gongora, Fabiola Ambrosio Silveira Lima, et al.
BMC Microbiology|July 17, 2016
E2 multimeric scaffold for vaccine formulation: immune response by intranasal delivery and transcriptome profile of E2-pulsed dendritic cellsMaria Trovato, Francesco Maurano, Luciana D'Apice, et al.
Journal of Surgical Oncology|June 2, 2004
Pelvic exenteration and sphincter preservation: an analysis of 96 casesAntonio Henrique Oliveira Poletto, Ademar Lopes, André Lopes Carvalho, et al.
Frontiers in Oncology|April 4, 2022
Breast Cancer Phenotype Associated With Li-Fraumeni Syndrome: A Brazilian Cohort Enriched by <i>TP53</i> p.R337H CarriersRenata Lazari Sandoval, Natalia Polidorio, Ana Carolina Rathsam Leite, et al.
Familial Cancer|April 30, 2024
A comprehensive characterization of the spectrum of MUTYH germline pathogenic variants in Latin AmericaPatricia Esperon, Florencia Neffa, Walter Pavicic, et al.
The Journal of Thoracic and Cardiovascular Surgery|October 29, 2008
The short esophagus: intraoperative assessment of esophageal lengthSandro Mattioli, Maria Luisa Lugaresi, Mario Costantini, et al.
BMC Cancer|September 24, 2015
Angiogenesis-related protein expression in bevacizumab-treated metastatic colorectal cancer: NOTCH1 detrimental to overall survivalTadeu Ferreira Paiva, Victor Hugo Fonseca de Jesus, Raul Amorim Marques, et al.
International Journal of Clinical Oncology|October 6, 2010
Pathologic complete response with neoadjuvant imatinib for locally advanced pelvic GISTCarla Rameri Alexandre Silva de Azevedo, Tadeu Ferreira Paiva, Benedito Mauro Rossi, et al.
Cancer Letters|February 24, 2006
The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian familiesMaria Isabel Waddington Achatz, Magali Olivier, Florence Le Calvez, et al.
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