Zobrazeno 1 - 10
of 36
pro vyhledávání: '"J. R. Gimeno"'
Autor:
V. Parisi, R. Baldassarre, V. Ferrara, R. Ditaranto, F. Barlocco, R. Lillo, F. Re, G. Marchi, C. Chiti, F. Di Nicola, C. Catalano, L. Barile, M. A. Schiavo, A. Ponziani, G. Saturi, A. G. Caponetti, A. Berardini, M. Graziosi, F. Pasquale, I. Salamon, M. Ferracin, E. Nardi, I. Capelli, D. Girelli, J. R. Gimeno Blanes, M. Biffi, N. Galiè, I. Olivotto, F. Graziani, E. Biagini
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundElectrocardiogram (ECG) has proven to be useful for early detection of cardiac involvement in Anderson-Fabry disease (AFD); however, little evidence is available on the association between ECG alterations and the progression of the disease.
Externí odkaz:
https://doaj.org/article/0241850bfd9049889039bb4c3205d153
Akademický článek
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Akademický článek
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Autor:
M Y C Van Der Heide, T E Verstraelen, F H M Van Lint, L P Bosman, R De Brouwer, V M Proost, T Germans, C Dickhoff, B A Schoonderwoerd, A C Houweling, J R Gimeno-Blanes, R A De Boer, M G P J Cox, P Van Tintelen, A A M Wilde
Publikováno v:
Europace. 25
Funding Acknowledgements Type of funding sources: Public Institution(s). Main funding source(s): PSIDER (ZOn-MW) PREDICT2 (Hartstichting) Background: The PLN p.Arg14del risk model is a mutation-specific risk model developed to predict individual mali
Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
M Van Der Heide, T E Verstraelen, F H M Van Lint, L P Bosman, R De Brouwer, V M Proost, G S Abeln, B A Schoonderwoerd, A C Houweling, J R Gimeno-Blanes, F W Asselbergs, R A De Boer, M P Van Den Berg, J P Van Tintelen, A A M Wilde
Publikováno v:
European Heart Journal. 43
Background/Introduction Recently, a variant-specific prediction model for PLN p.Arg14del variant carriers was developed to predict individual malignant ventricular arrhythmia (VA) risk to inform decision-making for primary prevention implantable card
Autor:
F Di Nicola, R Ditaranto, F Barlocco, R Lillo, F Re, G Marchi, R Baldassarre, V Parisi, V Ferrara, C Chiti, J R Gimeno Blanes, F Graziani, N Galie', I Olivotto, E Biagini
Publikováno v:
European Heart Journal. 43
Background Anderson-Fabry disease (AFD) is an X-linked lysosomal storage disorder that have gained attention due to the availability of therapeutic options. Disease specific therapy (DST), either by enzyme replacement therapy or oral pharmacological
Autor:
R Baldassarre, R Ditaranto, F Barlocco, R Lillo, F Re, G Marchi, V Parisi, V Ferrrara, F Di Nicola, C Chiti, J R Gimeno Blanes, F Graziani, N Galie', A Zancarano, E Biagini
Publikováno v:
European Heart Journal. 43
Background Anderson Fabry disease (AFD) is an X-linked lysosomal storage disorder leading to a deficiency in α-galactosidase A and globotriasylceramide (Gb3) deposition in different organs, including the heart. In AFD patients electrocardiogram (ECG
Autor:
A Protonotarios, R Barriales-Villa, L Antoniades, J Mogensen, P Garcia-Pavia, K Wahbi, E Biagini, A Anastasakis, A Tsatsopoulou, E Zorio, J R Gimeno, J M Garcia-Pinilla, G Sinagra, B Bauce, P M Elliott
Publikováno v:
European Heart Journal. 43
Introduction Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is associated with sudden cardiac death (SCD). The 2019 ARVC risk model has been proposed as a method to quantify arrhythmic risk, but the impact of genotype its performance has not
Autor:
M Garcia Perez-Carlos, F Martinez-Garcia, I San Roman-Monserrat, M Sabater-Molina, M Navarro-Penalver, C Gil-Ortuno, C Munoz-Esparza, J R Gimeno
Publikováno v:
European Heart Journal. 43
Backgroud Neuromuscular disorders may present with varied cardiac involvement, including myocardial and conduction tissue disease. Sudden death is a common adverse event of cardiomyopathy Purpose The objective was to present clinical characteristics