Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Cristina Brinckmann Oliveira Netto"'
Autor:
Clévia Rosset, Mariane da Cunha Jaeger, Eduardo Filippi-Chiela, Larissa Brussa Reis, Ivaine Taís Sauthier Sartor, Cristina Brinckmann Oliveira Netto, Caroline Brunetto de Farias, Rafael Roesler, Patricia Ashton-Prolla
Publikováno v:
Genetics and Molecular Biology, Vol 44, Iss 4 (2021)
Abstract Tuberous sclerosis complex (TSC) is an autosomal dominant cancer predisposition disorder caused by heterozygous mutations in TSC1 or TSC2 genes and characterized by mTORC1 hyperactivation. TSC-associated tumors develop after loss of heterozy
Externí odkaz:
https://doaj.org/article/fe7d672f066a416495abc777371618de
Autor:
Eriza Cristina Hahn, Camila Matzenbacher Bittar, Fernanda Sales Luis Vianna, Cristina Brinckmann Oliveira Netto, Jorge Villanova Biazús, Rodrigo Cericatto, José Antônio Cavalheiro, Márcia Portela de Melo, Carlos Henrique Menke, Eliane Rabin, Sandra Leistner-Segal, Patricia Ashton-Prolla
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0209934 (2018)
Premenopausal breast cancer (BC) is a core tumor of Li-Fraumeni (LFS) and Li-Fraumeni-like (LFL) Syndromes, predisposition disorders caused by germline mutations in TP53 gene. In the Southern and Southeastern regions of Brazil, a specific TP53 germli
Externí odkaz:
https://doaj.org/article/72fe0e8ab080464c9deefadbbc9ed3e4
Autor:
Bárbara Alemar, Cleandra Gregório, Josef Herzog, Camila Matzenbacher Bittar, Cristina Brinckmann Oliveira Netto, Osvaldo Artigalas, Ida Vanessa D Schwartz, Jordy Coffa, Suzi Alves Camey, Jeffrey Weitzel, Patricia Ashton-Prolla
Publikováno v:
PLoS ONE, Vol 13, Iss 5, p e0197529 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0187630.].
Externí odkaz:
https://doaj.org/article/0fc16c85890c46adaa059c560a8fccef
Autor:
Carmen Maria Dornelles Prolla, Patrícia Santos da Silva, Cristina Brinckmann Oliveira Netto, José Roberto Goldim, Patricia Ashton-Prolla
Publikováno v:
Revista Latino-Americana de Enfermagem, Vol 23, Iss 1, Pp 90-97 (2015)
OBJECTIVE: To assess the knowledge of nurses involved in the care of oncology patients in a public university hospital, regarding breast cancer and hereditary breast cancer, and to verify the use of such knowledge in their daily practice.METHODS: Thi
Externí odkaz:
https://doaj.org/article/d806cea7d44e45a1a696e18ae1bd9691
Autor:
Bárbara Alemar, Cleandra Gregório, Josef Herzog, Camila Matzenbacher Bittar, Cristina Brinckmann Oliveira Netto, Osvaldo Artigalas, Ida Vanessa D Schwartz, Jordy Coffa, Suzi Alves Camey, Jeffrey Weitzel, Patricia Ashton-Prolla
Publikováno v:
PLoS ONE, Vol 12, Iss 11, p e0187630 (2017)
BACKGROUND:Germline pathogenic variants in BRCA1 and BRCA2 (BRCA) are the main cause of Hereditary Breast and Ovarian Cancer syndrome (HBOC). METHODS:In this study we evaluated the mutational profile and prevalence of BRCA pathogenic/likely pathogeni
Externí odkaz:
https://doaj.org/article/297973dce97049bbb3e055ddb20ae46e
Autor:
Clévia Rosset, Filippo Vairo, Isabel Cristina Bandeira, Rudinei Luis Correia, Fernanda Veiga de Goes, Raquel Tavares Boy da Silva, Larissa Souza Mario Bueno, Mireille Caroline Silva de Miranda Gomes, Henrique de Campos Reis Galvão, João I C F Neri, Maria Isabel Achatz, Cristina Brinckmann Oliveira Netto, Patricia Ashton-Prolla
Publikováno v:
PLoS ONE, Vol 12, Iss 10, p e0185713 (2017)
Tuberous sclerosis complex (TSC) is an autosomal dominant multisystem disorder characterized by the development of multiple hamartomas in many organs and tissues. It occurs due to inactivating mutations in either of the two genes, TSC1 and TSC2, foll
Externí odkaz:
https://doaj.org/article/1664d8144a7346c39bd9e139dfa76002
Autor:
Tatiane Alves Vieira, Tatiéle Nalin, Bárbara Correa Krug, Camila Matzenbacher Bittar, Cristina Brinckmann Oliveira Netto, Ida Vanessa Doederlein Schwartz
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 3 (2015)
Introduction: Phenylketonuria (PKU) is caused by the deficient activity of phenylalanine hydroxylase. Aim: To identify the factors associated with treatment adherence among patients with PKU seen at a southern Brazil reference center. Methodology: A
Externí odkaz:
https://doaj.org/article/9499c25a43b243db8bce005fb204f366
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:
Antonio Milton Lima Garcia, Norma Martins Menezes Morais, Lygia Ohlweiler, Maria Isabel Bragatti Winckler, Josiane Ranzan, Osvaldo Alfonso Pinto Artigalás, Luise Lapagesse de Camargo Pinto, Cristina Brinckmann Oliveira Netto, Patrícia Ashton-Prolla, Leonardo Vedolin, Rudimar dos Santos Riesgo, Newra Tellechea Rotta
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 68, Iss 5, Pp 816-818 (2010)
Externí odkaz:
https://doaj.org/article/04039e53f5e0485eb1dea6b6470bdd4c
Autor:
José Augusto Bragatti, Carolina Machado Torres, Cristina Brinckmann Oliveira Netto, Leonardo Vedolin, Eliana Garzon, Carlos Roberto de Mello Rieder, Ida Vanessa Doederlein Schwartz, Marino Muxfeldt Bianchin
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 69, Iss 3, Pp 565-566 (2011)
Externí odkaz:
https://doaj.org/article/62550465cc694409bd0b3a07a870e0f4