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Evaluation of MLH1 variants of unclear significance.
Köger N, Paulsen L, López-Kostner F, Della Valle A, Vaccaro CA, Palmero EI, Alvarez K, Sarroca C, Neffa F, Kalfayan PG, Gonzalez ML, Rossi BM, Reis RM, Brieger A, Zeuzem S, Hinrichsen I, Dominguez-Valentin M, Plotz G. Köger N, et al. Among authors: rossi bm. Genes Chromosomes Cancer. 2018 Jul;57(7):350-358. doi: 10.1002/gcc.22536. Epub 2018 Apr 30. Genes Chromosomes Cancer. 2018. PMID: 29520894
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.
Park JG, Kim DW, Hong CW, Nam BH, Shin YK, Hong SH, Kim IJ, Lim SB, Aronson M, Bisgaard ML, Brown GJ, Burn J, Chow E, Conrad P, Douglas F, Dunlop M, Ford J, Greenblatt MS, Heikki J, Heinimann K, Lynch EL, Macrae F, McKinnon WC, Möeslein G, Rossi BM, Rozen P, Schofield L, Vaccaro C, Vasen H, Velthuizen M, Viel A, Wijnen J; International Society for Gastrointestinal Hereditary Tumours. Park JG, et al. Among authors: rossi bm. Clin Cancer Res. 2006 Jun 1;12(11 Pt 1):3389-93. doi: 10.1158/1078-0432.CCR-05-2452. Clin Cancer Res. 2006. PMID: 16740762
Mutation spectrum in South American Lynch syndrome families.
Dominguez-Valentin M, Nilbert M, Wernhoff P, López-Köstner F, Vaccaro C, Sarroca C, Palmero EI, Giraldo A, Ashton-Prolla P, Alvarez K, Ferro A, Neffa F, Caris J, Carraro DM, Rossi BM. Dominguez-Valentin M, et al. Among authors: rossi bm. Hered Cancer Clin Pract. 2013 Dec 18;11(1):18. doi: 10.1186/1897-4287-11-18. Hered Cancer Clin Pract. 2013. PMID: 24344984 Free PMC article.
Lynch syndrome in South America: past, present and future.
Vaccaro CA, Sarroca C, Rossi B, Lopez-Kostner F, Dominguez M, Calo NC, Cutait R, Valle AD, Nuñez L, Neffa F, Alvarez K, Gonzalez ML, Kalfayan P, Lynch HT, Church J. Vaccaro CA, et al. Fam Cancer. 2016 Jul;15(3):437-45. doi: 10.1007/s10689-016-9903-7. Fam Cancer. 2016. PMID: 27007491
The Development of the Study of Hereditary Cancer in South America.
Rossi BM, Sarroca C, Vaccaro C, Lopez F, Ashton-Prolla P, Ferreira Fde O, Santos EM. Rossi BM, et al. Genet Mol Biol. 2016 May 24;39(2):166-7. doi: 10.1590/1678-4685-GMB-2014-0366. Genet Mol Biol. 2016. PMID: 27223489 Free PMC article. No abstract available.
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America.
Rossi BM, Palmero EI, López-Kostner F, Sarroca C, Vaccaro CA, Spirandelli F, Ashton-Prolla P, Rodriguez Y, de Campos Reis Galvão H, Reis RM, Escremim de Paula A, Capochin Romagnolo LG, Alvarez K, Della Valle A, Neffa F, Kalfayan PG, Spirandelli E, Chialina S, Gutiérrez Angulo M, Castro-Mujica MDC, Sanchez de Monte J, Quispe R, da Silva SD, Rossi NT, Barletta-Carrillo C, Revollo S, Taborga X, Morillas LL, Tubeuf H, Monteiro-Santos EM, Piñero TA, Dominguez-Barrera C, Wernhoff P, Martins A, Hovig E, Møller P, Dominguez-Valentin M. Rossi BM, et al. Among authors: rossi nt. BMC Cancer. 2017 Sep 5;17(1):623. doi: 10.1186/s12885-017-3599-4. BMC Cancer. 2017. PMID: 28874130 Free PMC article.
Identification of hereditary cancer in the general population: development and validation of a screening questionnaire for obtaining the family history of cancer.
Campacci N, de Lima JO, Carvalho AL, Michelli RD, Haikel R Jr, Mauad E, Viana DV, Melendez ME, Vazquez FL, Zanardo C, Reis RM, Rossi BM, Palmero EI. Campacci N, et al. Among authors: rossi bm. Cancer Med. 2017 Dec;6(12):3014-3024. doi: 10.1002/cam4.1210. Epub 2017 Oct 21. Cancer Med. 2017. PMID: 29055968 Free PMC article.
76 results