Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Cinthia E. Jannes"'
Autor:
Elaine R. Coutinho, Marcio H. Miname, Viviane Z. Rocha, Marcio S. Bittencourt, Cinthia E. Jannes, Jose E. Krieger, Alexandre C. Pereira, Raul D. Santos
Publikováno v:
Atherosclerosis. 365:9-14
Autor:
José Eduardo Krieger, Mauricio Teruo Tada, Alexandre C. Pereira, Raquel Arroyo-Olivares, Ovidio Muñiz-Grijalvo, Luiza Antoniazzi, Márcio Sommer Bittencourt, Pedro Mata, José Luis Díaz-Díaz, Cinthia E. Jannes, Isabella Ramos Lima, Gracia M. Quintana-Navarro, Rodrigo Alonso, Raul D. Santos
Publikováno v:
Nutrition, Metabolism and Cardiovascular Diseases. 31:2014-2022
Familial Hypercholesterolemia (FH) is characterized by elevated LDL-cholesterol (LDL-C) and high atherosclerosis risk. The impact of different dietary patterns on atherosclerosis biomarkers has been poorly studied in FH. This study verified the assoc
Autor:
Karina Braga Gomes, Mauricio Teruo Tada, Júnea Paolucci de Paiva Silvino, Alexandre C. Pereira, Cinthia E. Jannes, Isabella Ramos Lima, Ieda de Fátima Oliveira Silva
Publikováno v:
Molecular Biology Reports. 47:9279-9288
Familial hypercholesterolemia (FH) is an autosomal dominant genetic disease characterized by high levels of low-density lipoprotein-cholesterol (LDLc), associated to premature cardiovascular disease. The detection of the variants related to FH is imp
Autor:
Joana Rita Chora, Margaret Chen, Lukáš Tichý, Sarah Leigh, Tomáš Freiberger, Michael A. Iacocca, Michal Kramarek, Robert A. Hegele, Hannah Wand, Cinthia E. Jannes, Liam R. Brunham, Heather Zimmermann, ClinGen Familial Hypercholesterolemia Expert Panel, Tami Johnston, Eric J.G. Sijbrands, Steve E. Humphries, Serra Kim, C. Lisa Kurtz, Alexandre C. Pereira, Mafalda Bourbon, Amanda J. Hooper, Jessica Chonis, Jian Wang, Mark Trinder, Joshua W. Knowles, Premysl Soucek, Maggie Williams, Annette Leon, Alain Carrié
Publikováno v:
Genetics in Medicine, 24(2), 293-306. Lippincott Williams & Wilkins
The online version of this article (https://doi.org/10.1016/j. gim.2021.09.012) contains supplementary material, which is available to authorized users. Purpose: In 2015, the American College of Medical Genetics and Genomics (ACMG) and the Associatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::339fef96974d58015c82ac362e1f9381
https://hdl.handle.net/10400.18/8289
https://hdl.handle.net/10400.18/8289
Autor:
Mauricio Teruo Tada, Pãmela Rodrigues de Souza Silva, Alexandre Costa Pereira, Isabella Ramos Lima, Theo G M Oliveira, Raul D. Santos, José Eduardo Krieger, Cinthia E. Jannes, Júnea Paolucci de Paiva Silvino
Publikováno v:
Arquivos Brasileiros de Cardiologia n.ahead 2022
Arquivos Brasileiros de Cardiologia
Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC
Arquivos Brasileiros de Cardiologia, Volume: 118, Issue: 4, Pages: 669-677, Published: 07 FEB 2022
Arquivos Brasileiros de Cardiologia (2022)
Arquivos Brasileiros de Cardiologia v.118 n.4 2022
Arquivos Brasileiros de Cardiologia
Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC
Arquivos Brasileiros de Cardiologia, Volume: 118, Issue: 4, Pages: 669-677, Published: 07 FEB 2022
Arquivos Brasileiros de Cardiologia (2022)
Arquivos Brasileiros de Cardiologia v.118 n.4 2022
Resumo Fundamento A hipercolesterolemia familiar (HF) é uma doença genética dominante que se caracteriza por níveis sanguíneos elevados de colesterol de lipoproteína de baixa densidade (LDL-C), e está associada à ocorrência de doença cardio
Autor:
Luciana Bahia, André Arpad Faludi, Valéria A. Machado, Roberta Marcondes Machado, Juliana Tieko Kato, Tania Leme da Rocha Martinez, Raul Dias dos Santos Filho, Elaine Dos Reis Coutinho, Francisco Antonio Helfenstein Fonseca, Adriana Bertolami, Andrei C. Sposito, Wilson Salgado Filho, Renato Jorge Alves, Ana Paula Marte Chacra, DB Araújo, Maria Cristina de Oliveira Izar, Cinthia E. Jannes, Marcelo Heitor Vieira Assad, Hermes Toros Xavier, Ana Maria Lottenberg, Antonio Carlos Palandri Chagas, Marcio H. Miname, Maria Silvia Ferrari Lavrador, Isabela de Carlos Back Giuliano, José Rocha Faria Neto, Fernando H. Y. Cesena, Isabela Cardoso Pimentel Mota, Dennys E. Cintra, Patrícia Guedes de Souza, Cristiane Kovacs Amaral, José Francisco Kerr Saraiva, Viviane Zorzanelli Rocha Giraldez, Marcelo Chiara Bertolami, Maria Helane Costa Gurgel Castelo
Publikováno v:
Arquivos Brasileiros de Cardiologia, Volume: 117, Issue: 4, Pages: 782-844, Published: 25 OCT 2021
Arquivos Brasileiros de Cardiologia, Vol 117, Iss 4, Pp 782-844 (2021)
Arquivos Brasileiros de Cardiologia, Vol 117, Iss 4, Pp 782-844 (2021)
Introduction Familial hypercholesterolemia (FH) is a common genetic cause of premature coronary artery disease (CAD), especially myocardial infarction, related to lifetime exposure to high concentrations of low-density lipoprotein cholesterol (LDL-C)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96311ce50074a5993224ec6a3b6770c4
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2021001200782&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2021001200782&lng=en&tlng=en
Autor:
José Osmar Medina Pestana, Taniela M Bes, Miguel Mitne-Neto, Silvia Figueiredo Costa, Carla M Dinardo, Alexandre C. Pereira, Cinthia E. Jannes, José Eduardo Krieger, Mariliza Velho, Alberto José da Silva Duarte, Karina Ramos Valino, Emanuelle Marques, Alexandre R Santos
The Covid-19 pandemic has changed the paradigms for disease surveillance and rapid deployment of scientific-based evidence for understanding disease biology, susceptibility, and treatment. We have organized a large-scale genome-wide association study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79acb20bf8e4c9cf0294c99b73e6ee17
https://doi.org/10.1101/2021.10.06.21264631
https://doi.org/10.1101/2021.10.06.21264631
Autor:
Pãmela Rodrigues de S. Silva, Cinthia E. Jannes, Theo G.M. Oliveira, José E. Krieger, Raul D. Santos, Alexandre C. Pereira
Publikováno v:
Journal of clinical lipidology. 16(2)
Familial hypercholesterolemia (FH) is an autosomal dominant disease characterized by the presence of high levels of total and low-density lipoprotein cholesterol (LDL-C). Statin treatment is recommended for all adults with FH.Here we have studied the
Autor:
Bruna, Los, Jéssica B, Borges, Victor F, Oliveira, Renata Cc, Freitas, Carolina, Dagli-Hernandez, Raul H, Bortolin, Rodrigo M, Gonçalves, André A, Faludi, Alice C, Rodrigues, Gisele M, Bastos, Cinthia E, Jannes, Alexandre C, Pereira, Rosario Dc, Hirata, Mario H, Hirata
Publikováno v:
Epigenomics. 13(10)
Autor:
Tomáš Freiberger, Heather Zimmermann, Michael A. Iacocca, Lukas Tichy, Cinthia E. Jannes, Robert A. Hegele, Michal Kramarek, Alain Carrié, Alexandre C. Pereira, Sarah Leigh, Joana Rita Chora, Eric J.G. Sijbrands, Margaret Chen, Hannah Wand, Serra Kim, C. Lisa Kurtz, Tami Johnston, Amanda J. Hooper, Steve E. Humphries, Mark Trinder, Liam R. Brunham, Mafalda Bourbon, Jessica Chonis, Jian Wang, Joshua W. Knowles, Premysl Soucek, Maggie Williams, Annette Leon
PurposeIn 2015, the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP) published consensus standardized guidelines for variant classification in Mendelian disorders. To increase accuracy and con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a865356915fa0402144210d466fbb6d2
https://doi.org/10.1101/2021.03.17.21252755
https://doi.org/10.1101/2021.03.17.21252755