Výsledky vyhledávání - "Benedito M. Rossi"

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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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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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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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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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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A novel germline mutation at exon 7 of the MSH2 gene (1249delG) in a large HNPCC Brazilian kindred Communicated by: R.G.H. Cotton Online Citation: Human Mutation, Mutation and Polymorphism Report #52 (1999) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr52.pdf Acknowledgments: We thank Ricardo P. Moura for technical assistance and the famiy that participated in this study. CMC holds a Brazilian Research Council (CNPq) post-doctoral fellowship

Autor: Cassandra M. Corvello, Roberta A.U. Bevilacqua, Benedito M. Rossi, Andrew J.G. Simpson

Publikováno v: Human Mutation. 13:506

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::437b7996402cf97e913a0f46d8c9b08c
https://doi.org/10.1002/(sici)1098-1004(1999)13:6<506::aid-humu17>3.3.co

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Akademický článek

Double‐barreled wet colostomy is a safe option for simultaneous urinary and fecal diversion. Analysis of 56 procedures from a single institution.

Autor: Gustavo C. Guimaraes, Fabio O. Ferreira, Benedito M. Rossi, Samuel Aguiar, Stenio C. Zequi, Wilson Bachega, Wilson T. Nakagawa, Francisco P. Fonseca, Alvaro S. Sarkis, Ademar Lopes

Publikováno v: Journal of Surgical Oncology; Feb2006, Vol. 93 Issue 3, p206-211, 6p

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