Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Patrícia Izetti"'
Autor:
Larissa Souza Mario Bueno, Clévia Rosset, Ernestina Aguiar, Fernando de Souza Pereira, Patrícia Izetti Ribeiro, Rosana Scalco, Camila Matzenbacher Bittar, Cristina Brinckmann Oliveira Netto, Guilherme Gischkow Rucatti, José Artur Chies, Suzi Alves Camey, Patricia Ashton-Prolla
Publikováno v:
International Journal of Endocrinology, Vol 2015 (2015)
Neurofibromatosis type 1 (NF1) patients are more likely to have vitamin D deficiency when compared to the general population. This study aimed to determine the levels of 25-OH-vitamin D [25(OH)D] in individuals with NF1 and disease-unaffected control
Externí odkaz:
https://doaj.org/article/e643fc55dfb546128979d52dae26d63a
Autor:
Gustavo Gössling, Rui D'Avila, Fernando de Souza Pereira, Patrícia Izetti, Marcos Antonio Freiberger Bassan, Gabriel Marques dos Anjos
Publikováno v:
Revista Brasileira de Ortopedia.
ResumoO osteoblastoma é uma doença benigna geralmente tratada com ressecção completa com intenção curativa e é responsável por 14% dos tumores ósseos benignos. Uma apresentação mais incomum refere-se a uma rápida apresentação em massa c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3c9d98efa31046572afa1960e2c8ec7
https://doi.org/10.1055/s-0041-1739300
https://doi.org/10.1055/s-0041-1739300
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
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
Publikováno v:
Genetics and Molecular Biology, Vol 39, Iss 2, Pp 223-231 (2016)
Abstract Approximately 5-10% of breast cancers are caused by germline mutations in high penetrance predisposition genes. Among these, BRCA1 and BRCA2, which are associated with the Hereditary Breast and Ovarian Cancer (HBOC) syndrome, are the most fr
Externí odkaz:
https://doaj.org/article/1d77d237f8334302a3adb2fb5bfe5798