Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Thais Bomfim"'
Autor:
Polyanna Oliveira, Paula Correa, Angelina Acosta, Juliana Freitas, Taísa Machado-Lopes, Thais Bomfim-Palma, Ândrea Ribeiro-dos-Santos, Sidney Santos, Roberto Nascimento, Ivana Nascimento, Kiyoko Abe-Sandes
Publikováno v:
Global Medical Genetics, Vol 10, Iss 04, Pp 376-381 (2023)
Introduction Cancer is a multifactorial disease dependent on the influence of genetic and environmental factors. About 10% of cancers are associated with germline mutations, which predispose to a higher risk of developing cancer. Currently, the use o
Externí odkaz:
https://doaj.org/article/07e37ab30a0f4284b513e8a1b03b0848
Autor:
Cagini, Nathália, Mansour, Eli, da Silva, Jane, Giavina-Bianchi, Pedro, Teixeira, Ana Júlia, Valle, Solange Rodrigues, Goudouris, Ekaterini, Serpa, Faradiba Sarquis, Moyses, Therezinha R., Campinhos, Fernanda Lugão, Ensina, Luis Felipe, Aranda, Carolina Sánchez, Rizzo, Maria Cândida, Campos, Régis A., Gonçalves, Rozana Fátima, Minafra, Fernanda Gontijo, de Souza Bernardes, Marli, Chong-Neto, Herberto José, Filho, Nelson Rosário, Guth, Carolina, Toledo, Eliana, Coelho Dias, Gabriela Andrade, Piccirillo, Miguel Alberto, Severo Ferreira, Janáira Fernandes, Marcelino, Fernanda Casares, da Rocha Rolins Neto, Pedro, Franco, Jackeline Motta, Pafume de Sá, Gustavo, Garro, Laila Sabino, Carolina da Matta Ain, Ana, Velasco, Helena F., Fernandes Carvalho, Ellaine Dóris, Fernandes Carvalho de Andrade, Maria Denise, Boll, Cristiane Alves, Ferraroni, Natasha Rebouças, Martins Pinto Swensson, Ana Carolina, Vilela Rabelo, Leandro Augusto, Pacheco de Figueiredo, Joanemile, Figueredo, Raphael Coelho, Mendes, Ronney Corrêa, Sales, Valéria S.F., Bacarini Leite, Luiz Fernando, Beltran Moschione Castro, Ana Paula, Ferreira Mascarenhas, Elke C., Teixeira, Thais Bomfim, Campos Teixeira, Camila A., Pereira de Lira Marques, Adriana, Pires Amaral Resende, Ludmilla Luzia, Sandrin, Leda das Neves Almeida, Tavares, Clarissa Soares, Veronez, Camila Lopes, Mendes, Agatha Ribeiro, Leite, Caroliny Souza, Gomes, Caio Perez, Grumach, Anete Sevciovic, Pesquero, João Bosco
Publikováno v:
In The Journal of Allergy and Clinical Immunology: In Practice June 2021 9(6):2293-2304
Autor:
Inês Élida Aguiar Bezerra, Nayara Balbino Gomes, Héryca Laiz Linhares Balica, Loide Cardoso Farias, Thais Bomfim Viana, Thalia Bomfim Viana
Publikováno v:
Educação e interdisciplinaridade: teoria e prática-Volume 3 ISBN: 9786525811765
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f87a27da74f8c68c35707d4a3cd023c3
https://doi.org/10.22533/at.ed.76523050423
https://doi.org/10.22533/at.ed.76523050423
Akademický článek
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Autor:
Karin Alvarez, Walter Hernán Pavicic, Taisa Manuela Bonfim Machado-Lopes, Tamara Alejandra Piñero, Maria Betânia Pereira Toralles, Francisco López-Köstner, Kiyoko Abe Sandes, Benedito Mauro Rossi, Carlos A. Vaccaro, Marion Rolain, Juliana Côrtes Freitas, Joanna Goes Castro Meira, Alexandra Martins, Thais Bomfim, Ivana Nascimento, Dirce Maria Carraro, Mev Dominguez-Valentin, Omar Soukarieh, Pål Møller, Giovana Tardin Torrezan, Samuel Aguiar Junior
Publikováno v:
Familial Cancer. 19:323-336
Germline pathogenic variants in the DNA mismatch repair genes (MMR): MLH1, MSH2, MSH6, and PMS2, are causative of Lynch syndrome (LS). However, many of the variants mapping outside the invariant splice site positions (IVS ± 1, IVS ± 2) are classifi
Autor:
Paula Francinete Faustino da Silva, Rebeca Mota Goveia, Thais Bomfim Teixeira, Bruno Faulin Gamba, Aliny Pereira de Lima, Sílvia Regina Rogatto, Ruffo de Freitas Júnior, Elisângela de Paula Silveira-Lacerda
Publikováno v:
Mastology.
Objective: We investigate the prevalence of TP53 germline pathogenic variants in a cohort of 83 breast cancer patients and 217 family members from the Midwest Brazilian region. Methods: All patients met the clinical criteria for hereditary breast and
Autor:
Márcia Cristiane Ferreira Mendes, Anaisa Alves de Moura, Vithória Alves de Moura, Thais Bomfim Viana
Publikováno v:
Educação e interdisciplinaridade: Teoria e prática
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c05aa7f308c9440ef23ac66ce537d113
https://doi.org/10.22533/at.ed.8082108091
https://doi.org/10.22533/at.ed.8082108091
Autor:
Rebeca Mota Goveia, Paula Francinete Faustino Silva, Thais Bomfim Teixeira, Isabela Gasparini Arraes, Ruffo Freitas-Júnior, Elisângela Paula Silveira- Lacerda
Publikováno v:
Mastology.
Introduction: Breast cancer is the most frequent type of cancer in the world and the biggest cause of female deaths. About 10%–15% of cases are due to hereditary factors. The profile of genetic variants is still scarcely known among the Brazilian p
Autor:
Gustavo Pafume de Sá, Leda das Neves Almeida Sandrin, Caio Perez Gomes, Regis A. Campos, Eliana de Toledo, Ana Paula Beltran Moschione Castro, Camila Lopes Veronez, Nelson Augusto Rosário Filho, Elke C. Ferreira Mascarenhas, Camila A. Campos Teixeira, Laila Sabino Garro, Solange Rodrigues Valle, Caroliny Souza Leite, Agatha Ribeiro Mendes, Fernanda Casares Marcelino, Leandro Augusto Vilela Rabelo, Ana Julia R. M. Teixeira, Anete Sevciovic Grumach, Fernanda Gontijo Minafra, Luiz Fernando Bacarini Leite, Carolina Sanchez Aranda, Nathália Cagini, Eli Mansour, Joanemile P. Figueiredo, Luis Felipe Ensina, Herberto José Chong-Neto, Clarissa Soares Tavares, Gabriela Andrade Coelho Dias, Pedro Rocha Rolins Neto, Raphael Coelho Figueredo, Pedro Giavina-Bianchi, Ronney Corrêa Mendes, Carolina Guth, Jackeline Motta Franco, Helena F. Velasco, Cristiane Alves Boll, Ekaterini Goudouris, Therezinha Ribeiro Moyses, Ellaine Dóris Fernandes Carvalho, Jane da Silva, Fernanda Lugão Campinhos, Faradiba Sarquis Serpa, Miguel Alberto Piccirillo, Rizzo Mc, M. Bernardes, Maria Denise Fernandes Carvalho de Andrade, Ana Carolina Martins Pinto Swensson, João Bosco Pesquero, Janaíra Fernandes Ferreira, Rozana Fátima Gonçalves, Valéria Soraya de Farias Sales, Ludmilla Luzia Pires Amaral Resende, Natasha Rebouças Ferraroni, Thais Bomfim Teixeira, Adriana Pereira de Lira Marques, Ana Carolina da Matta Ain
Publikováno v:
The journal of allergy and clinical immunology. In practice. 9(6)
Background Primary angioedema (PA) is a complex disorder, presenting multiple hereditary (hereditary angioedema) and acquired subtypes (acquired angioedema). Despite a very similar clinical presentation among subtypes, the differential diagnosis is l
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