Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Thuany Pinto Rocha De Souza"'
Autor:
Francisca Ladyssa Lima Moura, Thuany Pinto Rocha De Souza, Felipe Souza Da Silva, Maria Elena Nobre Soares, Isabelle Joyce de Lima Silva Fernandes
Publikováno v:
Brazilian Journal of Case Reports. 2:951-956
INTRODUÇÃO: Sabe-se o quão importante são as amostras de DNA para avaliação de tecido tu-moral. Tendo em vista que através da sua integridade pode-se ter bons resultados para análises de mutações gênicas. OBJETIVO: Avaliar a qualidade do D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19a8b7cecf9f622f6ab4fb6c1aec1bb0
https://doi.org/10.52600/2763-583x.bjcr.2022.2.suppl.3.951-956
https://doi.org/10.52600/2763-583x.bjcr.2022.2.suppl.3.951-956
Autor:
Francisca Fernanda Barbosa Oliveira, Anna Clara Aragão Matos Carlos, André Alves Crispim, Lívia Moreira Caetano Coelho, Cássia Emanuella Nóbrega Malta, Thuany Pinto Rocha de Souza, Isabelle Joyce de Lima Silva-Fernandes, Paulo Goberlânio de Barros Silva
Purpose To evaluate anxiety and spirituality levels in oncology patients during the coronavirus disease 2019 (COVID-19) pandemic. Methods This short-term cross-sectional study applied a previously validated General Anxiety Disorder-7 (GAD7) scale and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e49b85fb19f4730d815ca589b3414da
https://doi.org/10.21203/rs.3.rs-2177043/v1
https://doi.org/10.21203/rs.3.rs-2177043/v1
Autor:
Francisca Fernanda Barbosa Oliveira, Paulo Goberlânio de Barros Silva, Flávio da Silveira Bitencourt, Rosane Oliveira Sant'Ana, Isabelle Joyce de Lima Silva-Fernandes, Maria Júlia Barbosa Bezerra, Maria Claudia dos Santos Luciano, Clarissa Gondim Picanço-Albuquerque, Thuany Pinto Rocha de Souza, Marcos Venício Alves Lima
Publikováno v:
Journal of Clinical Oncology. 40:e22529-e22529
e22529 Background: Genetic tests have been increasingly requested to identify families at risk of hereditary cancer. In a family with a known mutation, the offspring of a carrier, whether male or female, have a 50% risk of inheriting the mutation. Mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4372a940a84553968962fb2d0ff028b
https://doi.org/10.1200/jco.2022.40.16_suppl.e22529
https://doi.org/10.1200/jco.2022.40.16_suppl.e22529
Autor:
Clarissa Gondim Picanço-Albuquerque, Rosane Oliveira Sant'Ana, Maria Claudia dos Santos Luciano, Maria Júlia Barbosa Bezerra, Flávio da Silveira Bitencourt, Francisca Fernanda Barbosa Oliveira, Thuany Pinto Rocha de Souza, Paulo Goberlânio de Barros Silva, Marcos Venício Alves Lima, Isabelle Joyce de Lima Silva-Fernandes
Publikováno v:
Journal of Clinical Oncology. 40:e22528-e22528
e22528 Background: The familiar history is indispensable to clinical investigation during genetic counseling and the new molecular techniques allowed the identification of hereditary cancer predisposition syndromes (CPS). However, the classification
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::592322ba6598364b891d798d983688b9
https://doi.org/10.1200/jco.2022.40.16_suppl.e22528
https://doi.org/10.1200/jco.2022.40.16_suppl.e22528