Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Natalia Quintella Sangiorgi Olivetti"'
Autor:
Gabrielle D'Arezzo Pessente, Luciana Sacilotto, Zaine Oliveira Calil, Natalia Quintella Sangiorgi Olivetti, Fanny Wulkan, Théo Gremen Mimary de Oliveira, Anísio Alexandre Andrade Pedrosa, Tan Chen Wu, Denise Tessariol Hachul, Maurício Ibrahim Scanavacca, José Eduardo Krieger, Francisco Carlos da Costa Darrieux, Alexandre da Costa Pereira
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
ObjectiveMutations in the Lamin A/C(LMNA) gene are commonly associated with cardiac manifestations, such as dilated cardiomyopathy (DCM) and conduction system disease. However, the overall spectrum and penetrance of rare LMNA variants are unknown. Th
Externí odkaz:
https://doaj.org/article/b5ed7aecce1c4981bb078599780a5c74
Autor:
Fabio Grunspun Pitta, Natalia Quintella Sangiorgi Olivetti, Diego Simões Peniche, Andrea Maria Dercht, Paulo Sampaio Gutierrez, Luiz Alberto Benvenuti
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 103, Iss 6, Pp e73-e80 (2014)
Externí odkaz:
https://doaj.org/article/5a8e293e419d4f648fd443ce254b9574
Autor:
Luciana Sacilotto, Natalia Quintella Sangiorgi Olivetti, Cristiano Faria Pisani, Tan Chen Wu, Ludhmila Abrahão Hajjar, Sissy Lara de Melo, Sávia Christina Pereira Bueno, Esteban Wisnivesky Rocca Rivarola, Muhieddine Omar Chokr, Carina Abigail Hardy, Denise Tessariol Hachul, Francisco Carlos da Costa Darrieux, Mauricio Ibrahim Scanavacca
Publikováno v:
Arquivos Brasileiros de Cardiologia
Resumo Desde dezembro de 2019, observamos o rápido avanço da síndrome respiratória aguda grave causada pelo coronavírus 2019 (SARS-CoV-2). O impacto da evolução clínica de uma infecção respiratória é pouco conhecido em pacientes portadore
Externí odkaz:
https://doaj.org/article/b3a1ed857d79484f8046df3a27bf1d8b
Autor:
Gabrielle D'Arezzo, Pessente, Luciana, Sacilotto, Zaine Oliveira, Calil, Natalia Quintella Sangiorgi, Olivetti, Fanny, Wulkan, Théo Gremen Mimary, de Oliveira, Anísio Alexandre Andrade, Pedrosa, Tan Chen, Wu, Denise Tessariol, Hachul, Maurício Ibrahim, Scanavacca, José Eduardo, Krieger, Francisco Carlos da Costa, Darrieux, Alexandre da Costa, Pereira
Publikováno v:
Frontiers in cardiovascular medicine. 9
Mutations in theOne-hundred and one consecutive patients with "lone AF" criteria were initially screened by genetic testing. Genetic variants were classified according to the American College of Genetic and Genomic criteria. All subjects were evaluat
Autor:
Silas Ramos Furquim, Bianca Linnenkamp, Natália Quintella Sangiorgi Olivetti, Fernando Rabioglio Giugni, Layara Fernanda Vicente Pereira Lipari, Fernanda Almeida Andrade, José Eduardo Krieger
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 120, Iss 10 (2023)
Resumo Os testes genéticos para cardiomiopatia dilatada (CMD) apresentam uma positividade de até 40%, mas há uma grande heterogeneidade genética e outros desafios decorrentes de expressividade variável e penetrância incompleta. O heredograma é
Externí odkaz:
https://doaj.org/article/2527e00e693f49b39d25bc15bb2cb87c
Autor:
Guilherme Augusto Teodoro Athayde, Natália Quintella Sangiorgi Olivetti, Francisco Carlos da Costa Darrieux, Luciana Sacilotto, Gabrielle D’Arezzo Pessente, Maurício Ibrahim Scanavacca
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 117, Iss 1 suppl 1, Pp 12-15 (2021)
Externí odkaz:
https://doaj.org/article/b5e679cbd1c9443fb43d683e889a4164
Autor:
Ana Carolina Guimarães Oliveira, Itamara Lucia Itagiba Neves, Luciana Sacilotto, Natália Quintella Sangiorgi Olivetti, Marcela Alves dos Santos‐Paul, Tânia Cristina Pedroso Montano, Cíntia Maria Alencar Carvalho, Tan Chen Wu, Cesar José Grupi, Sílvio Alves Barbosa, Carlos Alberto Pastore, Nelson Samesima, Denise Tessariol Hachul, Maurício Ibrahim Scanavacca, Ricardo Simões Neves, Francisco Carlos Costa Darrieux
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 8, Iss 15 (2019)
Background Brugada syndrome and long‐QT syndrome may account for at least one third of unexplained sudden cardiac deaths. Dental care in patients with cardiac channelopathies is challenging because of the potential risk of life‐threatening events
Externí odkaz:
https://doaj.org/article/5048d8c7ed8e4e2a838ecf629f99af52