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Dulce Brito

Showing results (11-20 of 123) with videos related to

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Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|December 13, 2005
Malignant mutations in hypertrophic cardiomyopathy: fact or fancy?Dulce Brito, Hugo Madeira
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|July 17, 2012
[The "broken heart syndrome": state of the art]Sofia Nóbrega, Dulce Brito
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|September 3, 2013
Severe heart disease in an unusual case of familial amyloid polyneuropathy type IMiguel Oliveira Santos, Dulce Brito
Revista Espanola De Cardiologia (English Ed.)|November 7, 2021
Fabry cardiomyopathy: what could parametric mapping still unveil?Luís Oliveira, Dulce Brito, João Abecasis
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|October 28, 2011
From hypertrophic cardiomyopathy centers to inherited cardiovascular disease centers in Europe. A small or a major step? A position paper from the Nucleus of the Working Group on Myocardial and Pericardial Diseases of the Portuguese Society of CardiologyNuno Cardim, António Freitas, Dulce Brito
European Journal of Heart Failure|August 9, 2002
How patients with heart failure are managed in PortugalCândida Fonseca, Fátima Ceia, Dulce Brito, et al.
The American Journal of Cardiology|July 9, 2013
Tissue Doppler imaging and plasma N-terminal probrain natriuretic peptide for the identification of hypertrophic cardiomyopathy mutation carriersDoroteia Silva, Hugo Madeira, Augusto Almeida, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|May 21, 2008
Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up studyDulce Brito, Pascale Richard, Michel Komajda, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|December 19, 2017
The potential of the inodilator levosimendan in maintaining quality of life in advanced heart failureMarkku S Nieminen, Cândida Fonseca, Dulce Brito, et al.
International Journal of Cardiology|December 18, 2018
Genetic characterization and genotype-phenotype associations in a large cohort of patients with hypertrophic cardiomyopathy - An ancillary study of the Portuguese registry of hypertrophic cardiomyopathyLuis Rocha Lopes, Dulce Brito, Adriana Belo, et al.
Pageof 13

Showing results (11-20 of 123) with videos related to

Sort By:
Pageof 13
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|December 13, 2005
Malignant mutations in hypertrophic cardiomyopathy: fact or fancy?Dulce Brito, Hugo Madeira
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|July 17, 2012
[The "broken heart syndrome": state of the art]Sofia Nóbrega, Dulce Brito
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|September 3, 2013
Severe heart disease in an unusual case of familial amyloid polyneuropathy type IMiguel Oliveira Santos, Dulce Brito
Revista Espanola De Cardiologia (English Ed.)|November 7, 2021
Fabry cardiomyopathy: what could parametric mapping still unveil?Luís Oliveira, Dulce Brito, João Abecasis
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|October 28, 2011
From hypertrophic cardiomyopathy centers to inherited cardiovascular disease centers in Europe. A small or a major step? A position paper from the Nucleus of the Working Group on Myocardial and Pericardial Diseases of the Portuguese Society of CardiologyNuno Cardim, António Freitas, Dulce Brito
European Journal of Heart Failure|August 9, 2002
How patients with heart failure are managed in PortugalCândida Fonseca, Fátima Ceia, Dulce Brito, et al.
The American Journal of Cardiology|July 9, 2013
Tissue Doppler imaging and plasma N-terminal probrain natriuretic peptide for the identification of hypertrophic cardiomyopathy mutation carriersDoroteia Silva, Hugo Madeira, Augusto Almeida, et al.
Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|May 21, 2008
Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up studyDulce Brito, Pascale Richard, Michel Komajda, et al.
European Heart Journal Supplements : Journal of the European Society of Cardiology|December 19, 2017
The potential of the inodilator levosimendan in maintaining quality of life in advanced heart failureMarkku S Nieminen, Cândida Fonseca, Dulce Brito, et al.
International Journal of Cardiology|December 18, 2018
Genetic characterization and genotype-phenotype associations in a large cohort of patients with hypertrophic cardiomyopathy - An ancillary study of the Portuguese registry of hypertrophic cardiomyopathyLuis Rocha Lopes, Dulce Brito, Adriana Belo, et al.
Pageof 13