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Page 1
Epidemiological characterization of rare diseases in Brazil: A retrospective study of the Brazilian Rare Diseases Network.
de Oliveira BM, Bernardi FA, Baiochi JF, Neiva MB, Artifon M, Vergara AA, Martins AM, Grumach AS, Acosta AX, Husny ASE, de Freitas Rodrigues Ribeiro B, Ramos CF, Steiner CE, Kim CA, Christofolini DM, Yamada DB, Carvalho EDF, Ribeiro EM, de Arruda Bastos F, Serpa FS, Brandão FR, Adjuto GMAF, Carvalho I, Saute JAM, Junior JCL, Bueno LSM, da Silva LCS, Santos MLSF, Costa MCM, Giusti MMCG, Galera MF, Filho MEC, de Andrade MDFC, De Oliveira Cardoso MT, de Menezes Ferreira MM, Zeny M, Caldato MCF, Sorte NB, Musolino NRC, de Medeiros PFV, Zen PRG, Da Silva RTB, Maia RE, Fock R, Almeida RES, Valle SOR, Amorim T, Teixeira TB, Prazeres VMG, de Faria Ferraz VE, Lima VC, Paiva WJM, Schwartz IVD, Alves D, Félix TM; Raras Network Group. de Oliveira BM, et al. Among authors: de faria ferraz ve. Orphanet J Rare Dis. 2024 Oct 30;19(1):405. doi: 10.1186/s13023-024-03392-7. Orphanet J Rare Dis. 2024. PMID: 39478612 Free PMC article.
Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population.
da Costa E Silva Carvalho S, Cury NM, Brotto DB, de Araujo LF, Rosa RCA, Texeira LA, Plaça JR, Marques AA, Peronni KC, Ruy PC, Molfetta GA, Moriguti JC, Carraro DM, Palmero EI, Ashton-Prolla P, de Faria Ferraz VE, Silva WA Jr. da Costa E Silva Carvalho S, et al. Among authors: de faria ferraz ve. BMC Med Genomics. 2020 Feb 10;13(1):21. doi: 10.1186/s12920-019-0652-y. BMC Med Genomics. 2020. PMID: 32039725 Free PMC article.
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers.
Fitarelli-Kiehl M, Giacomazzi J, Santos-Silva P, Graudenz MS, Palmero EI, Michelli RA, Achatz MI, de Toledo Osório CA, de Faria Ferraz VE, Picanço CG, Ashton-Prolla P. Fitarelli-Kiehl M, et al. Among authors: de faria ferraz ve. Fam Cancer. 2015 Jun;14(2):333-6. doi: 10.1007/s10689-015-9779-y. Fam Cancer. 2015. PMID: 25564201
Genetics and genomics in Brazil: a promising future.
Passos-Bueno MR, Bertola D, Horovitz DD, de Faria Ferraz VE, Brito LA. Passos-Bueno MR, et al. Among authors: de faria ferraz ve. Mol Genet Genomic Med. 2014 Jul;2(4):280-91. doi: 10.1002/mgg3.95. Mol Genet Genomic Med. 2014. PMID: 25077170 Free PMC article. No abstract available.
Erratum to: Genetic services and testing in Brazil.
Horovitz DD, de Faria Ferraz VE, Dain S, Marques-de-Faria AP. Horovitz DD, et al. Among authors: de faria ferraz ve. J Community Genet. 2013 Jul;4(3):377-8. doi: 10.1007/s12687-012-0108-y. J Community Genet. 2013. PMID: 22777608 Free PMC article.
Genetic services and testing in Brazil.
Horovitz DD, de Faria Ferraz VE, Dain S, Marques-de-Faria AP. Horovitz DD, et al. Among authors: de faria ferraz ve. J Community Genet. 2013 Jul;4(3):355-75. doi: 10.1007/s12687-012-0096-y. Epub 2012 May 5. J Community Genet. 2013. PMID: 22565417 Free PMC article. No abstract available.
Predictive models for mutations in mismatch repair genes: implication for genetic counseling in developing countries.
Monteiro Santos EM, Valentin MD, Carneiro F, de Oliveira LP, de Oliveira Ferreira F, Junior SA, Nakagawa WT, Gomy I, de Faria Ferraz VE, da Silva Junior WA, Carraro DM, Rossi BM. Monteiro Santos EM, et al. Among authors: de faria ferraz ve. BMC Cancer. 2012 Feb 9;12:64. doi: 10.1186/1471-2407-12-64. BMC Cancer. 2012. PMID: 22321913 Free PMC article.