Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fernanda Teresa de Lima"'
Autor:
Janaina Pontes Batista Cassoli, Ítalo Fernandes, Leonardo Carvalho, Milena Fernandes, Ana Fernanda Centrone, Letícia Taniwaki, Rita de Cássia Lima, Uelson Donizeti Rocioli Junior, Igor Wanderley Reis Dias, Patrícia Taranto, Juliana Beal, Fernanda Teresa de Lima, Fernando Moura, Miguel Cendoroglo, Sergio Eduardo Alonso Araújo, Pedro Luiz Serrano Uson Junior
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 8, Pp 7976-7985 (2024)
HER2-Low is defined as low levels of HER2 expression, based on a score of 1+ on immunohistochemical (IHC) assay or as an IHC score of 2+ and negative results on in situ hybridization (ISH or FISH). They are a heterogeneous population of breast cancer
Externí odkaz:
https://doaj.org/article/52b84d27bf344d359395fe078b4e965a
Autor:
Vandré Cabral Gomes Carneiro, Ana Carolina Leite Vieira Costa Gifoni, Benedito Mauro Rossi, Carlos Eduardo Mattos da Cunha Andrade, Fernanda Teresa de Lima, Henrique de Campos Reis Galvão, Jose Claudio Casali da Rocha, Leonardo Silveira da Silva Barreto, Patrícia Ashton‐Prolla, Rodrigo Santa Cruz Guindalini, Terence Pires de Farias, Wesley Pereira Andrade, Paulo Henrique de Sousa Fernandes, Reitan Ribeiro, Andre Lopes, Audrey Tieko Tsunoda, Bruno Roberto Braga Azevedo, Carlos Augusto Martinez Marins, Diego Nunes de Albuquerque Oliveira Uchôa, Evandro Airton Sordi Dos Santos, Felipe José Fernández Coimbra, Francisco Alcides Dias Filho, Francisco Carlos de Oliveira Lopes, Francisco Guilherme Fernandes, Guilherme Fonteles Ritt, Gustavo Andreazza Laporte, Gustavo Cardoso Guimaraes, Heládio Feitosa e Castro Neto, Jocela Cristina dos Santos, Jordana Botelho de Carvalho Vilela, Jorge Guardiola Meinhardt Junior, Juliano Rodrigues da Cunha, Leonardo Medeiros Milhomem, Luciana Mata da Silva, Luiza de Freitas Maciel, Nathalia Moreira Ramalho, Rafael Leite Nunes, Rodrigo Guido de Araújo, Rogério de Assunção Ehrhardt, Ronald Enrique Delgado Bocanegra, Tyrone Cesar Silva Junior, Viviane Rezende de Oliveira, Walyson Silva Surimã, Miriam de Melo Melquiades, Heber Salvador de Castro Ribeiro, Alexandre Ferreira Oliveira
Publikováno v:
Journal of Surgical Oncology. 126:10-19
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
Autor:
Francinne T. Tostes, Parisina Fraga Dutra Cabral de Carvalho, Raphael L. C. Araújo, Rodrigo Chaves Ribeiro, Franz Robert Apodaca-Torrez, Edson José Lobo, Diogo Bugano Diniz Gomes, Donato Callegaro-Filho, Gustavo Schvartsman, Fernando Moura, Vladimir Schraibman, Alberto Goldenberg, Fernanda Teresa de Lima, Vanderlei Segatelli, Pedro Luiz Serrano Uson Junior
Publikováno v:
Genes; Volume 13; Issue 10; Pages: 1809
Frantz tumors or solid pseudopapillary pancreatic neoplasm (SPN) are rare exocrine neoplasms that carry a favorable prognosis; they represent up to 3% of all tumors located in the region of the pancreas and have specific age and gender predisposition
Autor:
Fabricio T Romagnol, Eliana M Caran, Sérgio Cavalheiro, Marcelo de Toledo Petrilli, Henrique Manoel Lederman, Fernanda Teresa de Lima, Maria Teresa de Seixas Alves, Leticia Yasuda Carreira, Antonio Sérgio Petrilli
Publikováno v:
Clinical Oncology and Research. :1-6
This case report describes the outcomes of tropomyosin receptor kinase (TRK) inhibitor treatment in an infant with an infantile fibrosarcoma (IFS) with a TPM3–NTRK1 gene fusion. The IFS on the left foot was refractory to chemotherapy and was partia
Autor:
Elis Nogara Lisboa, Rita de Cassia Lima, Leticia Taniwaki, Rafael Aliosha Kaliks Guendelmann, Donato Callegaro Filho, Fernando Cotait Maluf, Fernanda Teresa de Lima
Publikováno v:
Mastology.
RAD51C is a gene associated with hereditary predisposition to ovarian cancer, and its association with hereditary breast cancer was controversial for a while. Current evidence demonstrates that RAD51C deleterious variants increase the risk of estroge
Autor:
Fernanda Teresa de Lima, Madeleyne Beatriz Boado Quiroga Cardenas, Gabriela de Almeida Vasconcelos Costa, Mary Miyazawa Simomoto, Afonso Celso Pinto Nazario, Joaquim Teodoro Araujo Neto, Wagner Antonio da Rosa Baratela, Gil Facina
Publikováno v:
Mastology.
Malignant breast neoplasm in men is rare, corresponding to less than 1% of all breast neoplasms, and 100 times less frequent than in women. It is molecularly different from female breast cancer, and germline pathogenic mutations in genes aside from B
Publikováno v:
A pluralidade do conhecimento na saúde, na educação e na tecnologia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f635fab1c961b827e027506800040183
https://doi.org/10.36229/978-65-5866-129-0.cap.07
https://doi.org/10.36229/978-65-5866-129-0.cap.07
Autor:
Sergio Cavalheiro, Andrea Cappellano, Daniela B Almeida, Frederico Adolfo Silva, Fernanda Teresa de Lima, Patricia Alessandra Dastoli, Milena R S Oliveira, Nasjla Saba da Silva
Publikováno v:
Neuro-Oncology
INTRODUCTION Choroid plexus tumors (CPT) are rare intraventricular neoplasms of epithelial origin. They usually occur in the 2nd year of life, corresponding to 0.4–0.6% of intracranial tumors in this age group. They are sub classified, according to
Autor:
Diego Miguel, Maria Isabel Achatz, Taisa Manuela Bonfim Machado-Lopes, Patricia Ashton-Prolla, Pricila Bernardi, Maria Nirvana Formiga, Jeffrey N. Weitzel, Ida Vanessa Doederlein Schwartz, José Bines, Bernardo Garicochea, Cristina Brinckmann Oliveira Netto, Miguel A. M. Moreira, Izabel Maria Monteiro Bernardes, Josef Herzog, Kiyoko Abe-Sandes, Maria Del Pilar Esteves-Diz, Sonia Tereza dos Santos Nogueira, Osvaldo Alfonso Pinto Artigalas, Maria Betânia Pereira Toralles, Gustavo Stumpf da Silva, Rafael Canfield Brianese, Fernando Regla Vargas, Patricia Santos-Silva, Sidney Santos, Anna Cláudia Evangelista dos Santos, Rommel Mario Rodriguez Burbano, Camila Matzenbacher Bittar, Sergio Daniel Simon, Thais Bomfim, Paulo Pimentel Assumpção, Ivana Nascimento, Terezinha Sarquis Cintra, Dirce Maria Carraro, Ana Carolina Leite Vieira Costa Gifoni, Cristiano de Pádua Souza, Anisse Marques Chami, Edenir Inêz Palmero, Kelly Rose Lobo de Souza, Barbara Alemar, Simone Noronha, Hector N. Seuanez, Ândrea Ribeiro-dos-Santos, Fabiana Baroni Alves Makdissi, Tirzah Braz Petta Lajus, Natalia Campacci, Rodrigo Santa Cruz Guindalini, Fernanda Teresa de Lima, Rui Manuel Reis, Henrique de Campos Reis Galvão
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Scientific Reports
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Scientific Reports
The detection of germline mutations in BRCA1 and BRCA2 is essential to the formulation of clinical management strategies, and in Brazil, there is limited access to these services, mainly due to the costs/availability of genetic testing. Aiming at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f64ae4cfd11cf4fced3cf336f2d7b3
https://hdl.handle.net/1822/58214
https://hdl.handle.net/1822/58214
Autor:
Vera Ayres Meloni, M. C. M. Oliveira, Sylvia Satomi Takeno, Fernanda Teresa de Lima, Maria Isabel Melaragno, Gianna Carvalheira
Publikováno v:
Meta Gene
Rearrangements in chromosome 19 are rare. Among the 35 patients with partial 19q trisomy described, only six have a breakpoint defined by array. The 19q duplication results in a variable phenotype, including dysmorphisms, intellectual disability and