Search Results - "EWALD, Ingrid Petroni"

Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil by Palmero, Edenir Inêz, Schüler-Faccini, Lavínia, Caleffi, Maira, Achatz, Maria Isabel Waddington, Olivier, Magali, Martel-Planche, Ghyslaine, Marcel, Virginie, Aguiar, Ernestina, Giacomazzi, Juliana, Ewald, Ingrid Petroni, Giugliani, Roberto, Hainaut, Pierre, Ashton-Prolla, Patricia

“…Abstract Germline TP53 mutations predispose to a rare familial cancer syndrome, the Li–Fraumeni Syndrome (LFS), characterized by the early onset of multiple…”
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IMPLEMENTATION OF ENHANCED RECOVERY AFTER COLORECTAL SURGERY (ERAS) PROTOCOL: INITIAL RESULTS OF THE FIRST BRAZILIAN EXPERIENCE by TEIXEIRA, Uirá Fernandes, FONTES, Paulo Roberto Ott, CONCEIÇÃO, Cristiane Weckerle Nazareth, FARIAS, Carlos Alberto Teixeira, FERNANDES, Daieni, EWALD, Ingrid Petroni, VITOLA, Luciano, MENDES, Florentino Fernandes

“…ABSTRACT Background: Guidelines for enhanced recovery after surgery have their bases in colonic surgery, through the first protocols published in 2012. Since…”
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BRCA1 and BRCA2 rearrangements in Brazilian individuals with Hereditary Breast and Ovarian Cancer Syndrome by Ewald, Ingrid Petroni, Cossio, Silvia Liliana, Palmero, Edenir Inez, Pinheiro, Manuela, Nascimento, Ivana Lucia de Oliveira, Machado, Taisa Manuela Bonfim, Sandes, Kiyoko Abe, Toralles, Betânia, Garicochea, Bernardo, Izetti, Patricia, Pereira, Maria Luiza Saraiva, Bock, Hugo, Vargas, Fernando Regla, Moreira, Miguel Ângelo Martins, Peixoto, Ana, Teixeira, Manuel R, Ashton-Prolla, Patricia

“…Approximately 5-10% of breast cancers are caused by germline mutations in high penetrance predisposition genes. Among these, BRCA1 and BRCA2, which are…”
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Genomic rearrangements in BRCA1 and BRCA2: A literature review by Ewald, Ingrid Petroni, Ribeiro, Patricia Lisboa Izetti, Palmero, Edenir Inêz, Cossio, Silvia Liliana, Giugliani, Roberto, Ashton-Prolla, Patricia

“…Women with mutations in the breast cancer genes BRCA1 or BRCA2 have an increased lifetime risk of developing breast, ovarian and other BRCA-associated cancers…”
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Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil by Palmero, Edenir Inêz, Alemar, Bárbara, Schüler-Faccini, Lavínia, Hainaut, Pierre, Moreira-Filho, Carlos Alberto, Ewald, Ingrid Petroni, Santos, Patricia Koehler Dos, Ribeiro, Patricia Lisbôa Izetti, Oliveira, Cristina Brinkmann de Netto, Calvez-Kelm, Florence Le, Tavtigian, Sean, Cossio, Silvia Liliana, Giugliani, Roberto, Caleffi, Maira, Ashton-Prolla, Patricia

“…In Brazil, breast cancer is a public health care problem due to its high incidence and mortality rates. In this study, we investigated the prevalence of…”
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Enhanced Recovery After Surgery®: resultados iniciales de la implementación del programa en cirugía de colon e hígado en Santa Casa de Porto Alegre, Brasil by Fernandes-Mendes, Florentino, Ott Fontes, Paulo Roberto, Vitola, Luciano, Nazareth Conceição, Cristiane Weckerle, Teixeira Farias, Carlos Alberto, Fernandes, Daieni, Petroni Ewald, Ingrid, Fernandes Teixeira, Uirá

“…El protocolo ERAS tiene como meta reducir la respuesta al estrés asociada a cirugía…”
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Screening and characterization of BRCA2 c.156_157insAlu in Brazil: Results from 1380 individuals from the South and Southeast by Felicio, Paula Silva, Alemar, Barbara, Coelho, Aline Silva, Berardinelli, Gustavo Noriz, Melendez, Matias Eliseo, Lengert, André Van Helvoort, Miche lli, Rodrigo Depieri, Reis, Rui M., Fernandes, Gabriela Carvalho, Ewald, Ingrid Petroni, Bittar, Camila Matzenbacher, Netto, Cristina Brinckmann Oliveira, Artigalas, Osvaldo, Peixoto, Ana, Pinheiro, Manuela, Teixeira, Manuel R., Vargas, Fernando Regla, dos Santos, Anna Cláudia Evangelista, Moreira, Miguel Angelo Martins, Ashton-Prolla, Patricia, Palmero, Edenir Inêz

“…•In our cohort, the frequency of the Portuguese BRCA2 founder mutation (c.156_157insAlu) was 0.65%.•The most frequent ancestry proportions of the mutation…”
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Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion by Silva, Amanda Gonçalves, Ewald, Ingrid Petroni, Sapienza, Marina, Pinheiro, Manuela, Peixoto, Ana, de Nóbrega, Amanda França, Carraro, Dirce M, Teixeira, Manuel R, Ashton-Prolla, Patricia, Achatz, Maria Isabel W, Rosenberg, Carla, Krepischi, Ana C V

“…Li-Fraumeni (LFS) and Li-Fraumeni-like (LFL) syndromes are associated to germline TP53 mutations, and are characterized by the development of central nervous…”
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BRCA1 and BRCA2 rearrangements in Brazilian individuals with Hereditary Breast and Ovarian Cancer Syndrome by Ingrid Petroni Ewald, Silvia Liliana Cossio, Edenir Inez Palmero, Manuela Pinheiro, Ivana Lucia de Oliveira Nascimento, Taisa Manuela Bonfim Machado, Kiyoko Abe Sandes, Betânia Toralles, Bernardo Garicochea, Patricia Izetti, Maria Luiza Saraiva Pereira, Hugo Bock, Fernando Regla Vargas, Miguel Ângelo Martins Moreira, Ana Peixoto, Manuel R. Teixeira, Patricia Ashton-Prolla

“…Abstract Approximately 5-10% of breast cancers are caused by germline mutations in high penetrance predisposition genes. Among these, BRCA1 and BRCA2, which…”
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Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil by Edenir Inêz Palmero, Bárbara Alemar, Lavínia Schüler-Faccini, Pierre Hainaut, Carlos Alberto Moreira-Filho, Ingrid Petroni Ewald, Patricia Koehler dos Santos, Patricia Lisbôa Izetti Ribeiro, Cristina Brinkmann de Oliveira Netto, Florence Le Calvez-Kelm, Sean Tavtigian, Silvia Liliana Cossio, Roberto Giugliani, Maira Caleffi, Patricia Ashton-Prolla

“…Abstract In Brazil, breast cancer is a public health care problem due to its high incidence and mortality rates. In this study, we investigated the prevalence…”
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