Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Fanny Wulkan"'
Autor:
Fanny Wulkan, Rocco Romagnuolo, Beiping Qiang, Tamilla Valdman Sadikov, Kyung-Phil Kim, Elya Quesnel, Wenlei Jiang, Naaz Andharia, Jill J. Weyers, Nilesh R. Ghugre, Bilgehan Ozcan, Faisal J. Alibhai, Michael A. Laflamme
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundHuman pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) show tremendous promise for cardiac regeneration following myocardial infarction (MI), but their transplantation gives rise to transient ventricular tachycardia (VT) in large-ani
Externí odkaz:
https://doaj.org/article/0c3a1bff478443819665f3585f74ddc7
Autor:
Natália Olivetti, Luciana Sacilotto, Danilo Bora Moleta, Lucas Arraes de França, Lorena Squassante Capeline, Fanny Wulkan, Tan Chen Wu, Gabriele D’Arezzo Pessente, Mariana Lombardi Peres de Carvalho, Denise Tessariol Hachul, Alexandre da Costa Pereira, José E. Krieger, Mauricio Ibrahim Scanavacca, Marcelo Luiz Campos Vieira, Francisco Darrieux
Publikováno v:
Diagnostics, Vol 14, Iss 2, p 150 (2024)
Introduction: The echocardiographic diagnosis criteria for arrhythmogenic right ventricular cardiomyopathy (ARVC) are highly specific but sensitivity is low, especially in the early stages of the disease. The role of echocardiographic strain in ARVC
Externí odkaz:
https://doaj.org/article/e6eae6b9f4f34f7f8244e1f144434175
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:
Luciana Sacilotto, Hindalis Ballesteros Epifanio, Francisco Carlos da Costa Darrieux, Fanny Wulkan, Theo Gremen Mimary Oliveira, Denise Tessariol Hachul, Alexandre da Costa Pereira, Mauricio Ibrahim Scanavacca
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 108, Iss 1, Pp 70-73
Abstract Compound heterozygosity has been described in inherited arrhythmias, and usually associated with a more severe phenotype. Reports of this occurrence in Brugada syndrome patients are still rare. We report a study of genotype-phenotype correla
Externí odkaz:
https://doaj.org/article/129e081ca20a41d589b335d86c574a78
Autor:
Wahiba Dhahri, Tamilla Sadikov Valdman, Dan Wilkinson, Elizabeth Pereira, Eylül Ceylan, Naaz Andharia, Beiping Qiang, Hassan Masoudpour, Fanny Wulkan, Elya Quesnel, Wenlei Jiang, Shunsuke Funakoshi, Amine Mazine, M. Juliana Gomez-Garcia, Neda Latifi, Yidi Jiang, Ella Huszti, Craig A. Simmons, Gordon Keller, Michael A. Laflamme
Publikováno v:
Circulation
Background: Human pluripotent stem cell (hPSC)–derived cardiomyocytes (hPSC-CMs) have tremendous promise for application in cardiac regeneration, but their translational potential is limited by an immature phenotype. We hypothesized that large-scal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d62ab5c4f7e0d9d31c18f26824aa728
https://doi.org/10.1161/circulationaha.121.053563
https://doi.org/10.1161/circulationaha.121.053563
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2485
The transplantation of human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) has garnered significant attention as a potential means of restoring lost muscle mass and contractile function in injured hearts. Early preclinical work with hPSC-CM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ee6153c9f356d750931ae856f90013ba
https://pubmed.ncbi.nlm.nih.gov/35618907
https://pubmed.ncbi.nlm.nih.gov/35618907
Publikováno v:
Advanced Technologies in Cardiovascular Bioengineering ISBN: 9783030861391
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a20da8e3625bdbc80431d041ab818c7a
https://doi.org/10.1007/978-3-030-86140-7_14
https://doi.org/10.1007/978-3-030-86140-7_14
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ea1558dc7265fc5644e797e3aaa060c2
https://pubmed.ncbi.nlm.nih.gov/35449878
https://pubmed.ncbi.nlm.nih.gov/35449878
Autor:
Hassan Masoudpour, Michael A. Laflamme, Eylul Ceylan, Tamilla Sadikov Valdman, Fanny Wulkan, Beiping Qiang, Wahiba Dhahri
Publikováno v:
Circulation Research. 127
Human embryonic stem cell-derived cardiomyocytes (hESC-CMs) have tremendous promise for application in cardiac repair, but their immature phenotype greatly limits their translational potential. The present study was designed to two hypotheses: 1) tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::307f5fd58b689c6f8e0c9c7777496e87
https://doi.org/10.1161/res.127.suppl_1.291
https://doi.org/10.1161/res.127.suppl_1.291
Autor:
Carolina Lemes, Mauricio Scanavacca, Alexandre C. Pereira, Denise Hachul, Natália Olivetti, Francisco Darrieux, José Eduardo Krieger, Luciana Sacilotto, Fanny Wulkan, Gabrielle D’Arezzo Pessente
Publikováno v:
Journal of cardiovascular electrophysiologyREFERENCES. 31(11)
BACKGROUND Brugada syndrome (BrS) has diagnostic challenges and controversial risk assessment. We aimed to investigate invasive and noninvasive parameters in symptomatic and asymptomatic patients from a Brazilian cohort of type-1 BrS. METHODS Patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::181d3d6825e2093ef40b00ea9b61db15
https://pubmed.ncbi.nlm.nih.gov/32870548
https://pubmed.ncbi.nlm.nih.gov/32870548