Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jorge Luiz Albuquerque, Coutinho"'
Autor:
Ernesto Curty, Fernando Eugênio dos Santos Cruz, Fabiane Santos Lima, Jorge Luiz Albuquerque Coutinho, Rosane Silva, Turán Peter Ürményi, Antônio Carlos Campos Carvalho, Edson Rondinelli
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 96, Iss 3, Pp 172-178 (2011)
FUNDAMENTO: A síndrome do QT longo (SQTL) é uma síndrome arrítmica herdada com aumento do intervalo QT e risco de morte súbita. Mutações nos genes KCNQ1, KCNH2 e SCN5A respondem por 90% dos casos com genótipo determinado, e a genotipagem é i
Externí odkaz:
https://doaj.org/article/1cf5998e8d284b7797be5a0402cb72c3
Autor:
S. Policarpo, Jorge Luiz Albuquerque Coutinho, Armando Carvalho, Isabel Medeiros, Francisco Velasco, Ana Catarina Alves, Mafalda Bourbon, Mariana V. Machado, Helena Cortez-Pinto, Sofia Carvalhana, Jorge Leitão, Ana P. Silva
Publikováno v:
Obesity Surgery. 30:560-568
Introduction: Nonalcoholic fatty liver disease (NAFLD) is the liver manifestation of adiposopathy. Recently, a new score was developed to estimate body fat percentage (relative fat mass, RFM). We aimed to evaluate the value of RFM in predicting the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60280f51004fda7bee45c07187c62e43
https://doi.org/10.1007/s11695-019-04213-8
https://doi.org/10.1007/s11695-019-04213-8
Autor:
Isadora M. Vaz, Tais Hanae Kasai-Brunswick, J.C.G. Oliveira, Rodrigo S. Moura-Neto, Prs Brofman, Dayana S. Araujo, A.C. Campos-de-Carvalho, Jorge Luiz Albuquerque Coutinho, R.P. Ferreira, Glauber Monteiro Dias, Fernanda Gubert, Tamara Borgonovo, R. Silva, Adriana Bastos Carvalho, D. Silva dos Santos, Eduardo Back Sternick, F.E.S.F. Cruz
Publikováno v:
Stem Cell Research, Vol 31, Iss, Pp 174-180 (2018)
Four human iPSC cell lines (one Jervell and Lange-Nielsen Syndrome, one Long QT Syndrome-type 1 and two healthy controls) were generated from peripheral blood obtained from donors belonging to the same family. CytoTune™-iPS 2.0 Sendai Reprogramming
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61000fa42e5f4d26cb0e81a7282c837e
https://doi.org/10.1016/j.scr.2018.07.016
https://doi.org/10.1016/j.scr.2018.07.016
Autor:
Bruna Farjun, Daiana S Araujo, Antonio Carlos Carvalho, Isadora M. Vaz, Tais H Brunswick, Danúbia Silva dos Santos, R.P. Ferreira, Adriana Bastos Carvalho, Tamara Brogonovo, Glauber Monteiro Dias, Isabela de Carvalho Leitão, Fernando Cruz, Jorge Luiz Albuquerque Coutinho
Publikováno v:
Circulation Research. 125
The purpose of this work was to investigate if iPSC derived cardiomyocytes would reproduce the divergent phenotypes observed in a proband and mother that carried the same likely-pathogenic variant in KCNQ1 gene. A 15 years old proband had syncope and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d88cb14d1e9bd2436acc580f3be5054
https://doi.org/10.1161/res.125.suppl_1.209
https://doi.org/10.1161/res.125.suppl_1.209
Autor:
Adriana Bastos Carvalho, Bruna Farjun, R Pires-Ferreira, Isadora M. Vaz, Fes Cruz-Filho, Tais Hanae Kasai-Brunswick, AC Campos-de-Carvalho, Tamara Borgonovo, Dayana S. Araujo, Raq Barbosa, Glauber Monteiro Dias, Jorge Luiz Albuquerque Coutinho, Danubia Silva-dos-Santos
Publikováno v:
Cytotherapy. 23:27
Background Human induced pluripotent stem (iPS) cell-derived cardiomyocytes (hiPSC‐CMs) technology offers an unprecedented tool to study cardiac diseases. Long QT syndrome type 1 (LQT1) is an inherited cardiac channelopathy caused by mutations in K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::736672a0b0ff3d7a9a950030479acba8
https://doi.org/10.1016/j.jcyt.2021.02.080
https://doi.org/10.1016/j.jcyt.2021.02.080
Autor:
Turán P. Ürményi, Antônio Carlos Campos Carvalho, Edson Rondinelli, Ernesto Curty, Jorge Luiz Albuquerque Coutinho, Rosane Silva, Fernando Cruz, Fabiane Santos Lima
Publikováno v:
Arquivos Brasileiros de Cardiologia v.96 n.3 2011
Arquivos Brasileiros de Cardiologia
Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC
Arquivos Brasileiros de Cardiologia, Vol 96, Iss 3, Pp 172-178 (2011)
Arquivos Brasileiros de Cardiologia, Volume: 96, Issue: 3, Pages: 172-178, Published: 04 FEB 2011
Arquivos Brasileiros de Cardiologia
Sociedade Brasileira de Cardiologia (SBC)
instacron:SBC
Arquivos Brasileiros de Cardiologia, Vol 96, Iss 3, Pp 172-178 (2011)
Arquivos Brasileiros de Cardiologia, Volume: 96, Issue: 3, Pages: 172-178, Published: 04 FEB 2011
FUNDAMENTO: A síndrome do QT longo (SQTL) é uma síndrome arrítmica herdada com aumento do intervalo QT e risco de morte súbita. Mutações nos genes KCNQ1, KCNH2 e SCN5A respondem por 90% dos casos com genótipo determinado, e a genotipagem é i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35a93869e50fb05c61f4ff3582a8bfe6
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2011000300002
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0066-782X2011000300002
Autor:
Curty, Ernesto, Fernando Eugênio dos Santos, Cruz, Fabiane Santos, Lima, Jorge Luiz Albuquerque, Coutinho, Rosane, Silva, Turán Peter, Urményi, Antônio Carlos Campos, Carvalho, Edson, Rondinelli
Publikováno v:
Arquivos brasileiros de cardiologia. 96(3)
The long QT syndrome (LQTS) is an inherited arrhythmia syndrome with increased QT interval and risk of sudden death. Mutations in genes KCNQ1, KCNH2 and SCN5A account for 90% of cases with genotype determined, and genotyping is informative for geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f635235e4c0851565dc1cf4b1b10d4d3
https://pubmed.ncbi.nlm.nih.gov/21308345
https://pubmed.ncbi.nlm.nih.gov/21308345