Zobrazeno 1 - 10 of 22 pro vyhledávání: '"Benedito M. Rossi"'
1
Akademický článek
Genotype‐phenotype correlation in 99 familial adenomatous polyposis patients: A prospective prevention protocol
Autor: Junea C. de Oliveira, Danilo V. Viana, Cleyton Zanardo, Erika M. M. Santos, André E. de Paula, Edenir I. Palmero, Benedito M. Rossi
Publikováno v: Cancer Medicine, Vol 8, Iss 5, Pp 2114-2122 (2019)
Abstract Background Familial adenomatous polyposis (FAP) is a syndrome caused by germline pathogenic variants in the tumor suppressor gene adenomatous polyposis coli (APC). Identification of APC pathogenic variants sites and the genotype‐phenotype
Externí odkaz: https://doaj.org/article/9cba22f40c924004835e8a01de599ccf
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2
Cancer risk‐reducing surgery: Brazilian Society of Surgical Oncology Guideline Part 2 (Gastrointestinal and thyroid)
Autor: Vandré C. G. Carneiro, Ana C. L. V. C. Gifoni, Benedito M. Rossi, Carlos E. M. da Cunha Andrade, Fernanda T. de Lima, Henrique de Campos Reis Galvão, Jose C. C. da Rocha, Leonardo S. da Silva Barreto, Patrícia Ashton‐Prolla, Rodrigo S. C. Guindalini, Terence P. de Farias, Wesley P. Andrade, Paulo H. de Sousa Fernandes, Reitan Ribeiro, Andre Lopes, Audrey T. Tsunoda, Bruno R. B. Azevedo, Carlos A. M. Marins, Diego N. de Albuquerque Oliveira Uchôa, Evandro A. S. Dos Santos, Felipe J. F. Coimbra, Francisco A. D. Filho, Francisco C. de Oliveira Lopes, Francisco G. Fernandes, Guilherme F. Ritt, Gustavo A. Laporte, Gustavo C. Guimaraes, Heládio Feitosa e Castro Neto, Jocela C. dos Santos, Jordana B. de Carvalho Vilela, Jorge G. M. Junior, Juliano R. da Cunha, Leonardo M. Milhomem, Luciana M. da Silva, Luiza de Freitas Maciel, Nathalia M. Ramalho, Rafael L. Nunes, Rodrigo G. de Araújo, Rogério de Assunção Ehrhardt, Ronald E. D. Bocanegra, Tyrone C. S. Junior, Viviane R. de Oliveira, Walyson S. Surimã, Miriam de Melo Melquiades, Heber S. de Castro Ribeiro, Alexandre F. Oliveira
Publikováno v: Journal of Surgical Oncology. 126:20-27
Risk-reducing operations are an important part of the management of hereditary predisposition to cancer. In selected cases, they can considerably reduce the morbidity and mortality associated with cancer in this population.The Brazilian Society of Su
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48af3b118781cc711359781f187f303c
https://doi.org/10.1002/jso.26813
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3
Contribution of rare germline copy number variations and common susceptibility loci in Lynch syndrome patients negative for mutations in the mismatch repair genes
Autor: Rolando A R, Villacis, Priscila M, Miranda, Israel, Gomy, Erika M M, Santos, Dirce M, Carraro, Maria I, Achatz, Benedito M, Rossi, Silvia R, Rogatto
Publikováno v: International journal of cancer. 138(8)
In colorectal carcinoma (CRC), 35% of cases are known to have a hereditary component, while a lower proportion (∼ 5%) can be explained by known genetic factors. In this study, copy number variations (CNVs) were evaluated in 45 unrelated patients wi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d922a2460c9ae0efa8aa48a73999b207
https://pubmed.ncbi.nlm.nih.gov/26620301
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4
Prognostic factors in locally advanced colon cancer treated by extended resection Fatores prognósticos em câncer de cólon localmente avançado tratado com ressecção extendida
Autor: René A.C. Vieira, Ademar Lopes, Paulo A.C. Almeida, Benedito M. Rossi, Wilson T. Nakagawa, Fabio O. Ferreira, Celso A. Melo
Publikováno v: Revista do Hospital das Clínicas, Vol 59, Iss 6, Pp 361-368 (2004)
The impact of clinical, pathologic, and surgical variables on the postoperative morbidity, mortality, and survival of patients undergoing extended resections of colon carcinoma were evaluated. METHODS: The medical records of 95 patients who underwent
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doajarticles::093067b2156a6443a4b31407f600eb5a
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812004000600009
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5
Less DeltamtDNA4977 than normal in various types of tumors suggests that cancer cells are essentially free of this mutation
Autor: Maria Angela C, Dani, Sergio U, Dani, Silmara P G, Lima, Alfredo, Martinez, Benedito M, Rossi, Fernando, Soares, Marco A, Zago, Andrew J G, Simpson
Publikováno v: Genetics and molecular research : GMR. 3(3)
Levels of mtDNA(4977) deletions (DeltamtDNA(4977)) have been found to be lower in tumors than in adjacent non-tumoral tissues. In 87 cancer patients, DeltamtDNA(4977) was detected by multiplex polymerase chain reaction (PCR) amplification in 43 (49%)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bf8dcbf1c634e93c7b769284d7f428d6
https://pubmed.ncbi.nlm.nih.gov/15614730
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10
Akademický článek
Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients.
Autor: Silva, Felipe C.1 felipe.silva@accamargo.org.br, Lisboa, Bianca C. G.1 lisboa.bianca@gmail.com, Figueiredo, Marcia C. P.1 marcia.figueiredo@accamargo.org.br, Torrezan, Giovana T.1 giovana.torrezan@accamargo.org.br, Santos, Érika M. M.2 erikammsantos@gmail.com, Krepischi, Ana C.1,3 ana.krepischi@gmail.com, Rossi, Benedito M.2 rossibm@gmail.com, Achatz, Maria I.3,4 miachatz@cipe.accamargo.org.br, Carraro, Dirce M.1,3 dirce.carraro@cipe.accamargo.org.br
Publikováno v: BMC Medical Genetics. 2014, Vol. 15 Issue 1, p1-24. 24p.
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