Works matching IS 20358253 AND DT 2013 AND VI 3 AND IP 1

Results: 10

Cost-effectiveness of genetic studies in inherited heart diseases.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 28, doi. 10.4081/cardiogenetics.2013.e5

By:

Sabater-Molina, María;
García-Molina, Esperanza;
Tovar, Isabel;
Ruiz-Espejo, Francisco;
Gimeno, Juan Ramón;
Valdés, Mariano

Publication type:

Article

Atrial fibrillation is poorly tolerated by patients with hypertrophic concentric cardiomyopathy caused by mitochondrial tRNA<sup>Leu (UUR)</sup> mutations.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 31, doi. 10.4081/cardiogenetics.2013.e6

By:

Heliö, Tiina M.;
Götz, Alexandra;
Rapola, Janne;
Kiuru-Enari, Sari;
Kivistö, Sari;
Heikinheimo, Terttu;
Suomalainen, Anu

Publication type:

Article

Lamin A/C mutation affecting primarily the right side of the heart.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 1, doi. 10.4081/cardiogenetics.2013.e1

By:

Ollila, Laura;
Kuusisto, Johanna;
Peuhkurinen, Keijo;
Kärkkäinen, Satu;
Tuomainen, Petri;
Kaartinen, Maija;
Raheem, Olayinka;
Udd, Bjarne;
Magga, Jarkko;
Rapola, Janne;
Lahtinen, Annukka M.;
Lehtonen, Eero;
Holmström, Miia;
Kivistö, Sari;
Widén, Elisabeth;
Saksa, Markku;
Heliö, Tiina

Publication type:

Article

Echocardiography in Fabry disease.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 17, doi. 10.4081/cardiogenetics.2013.e3

By:

Niemann, Markus;
Weidemann, Frank

Publication type:

Article

Myocardial deformation imaging and rare cardiomyopathies with hypertrophic phenotype: a review focused on Fabry disease, Friedreich ataxia and amyloidosis.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 22, doi. 10.4081/cardiogenetics.2013.e4

By:

Fadel, Bahaa;
Baldini, Luca;
Pergola, Valeria;
Bulbul, Ziad Al;
Di Salvo, Giovanni

Publication type:

Article

J wave syndromes as a cause of sudden arrhythmic death.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 8, doi. 10.4081/cardiogenetics.2013.e2

By:

Antzelevitch, Charles

Publication type:

Article

Imaging in Rare Disease: a roadmap for diagnosis.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 55, doi. 10.4081/cardiogenetics.2013.e10

By:

Di Salvo, Giovanni;
Limongelli, Giuseppe

Publication type:

Article

Muscular dystrophies: key elements for everyday diagnosis and management.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 49, doi. 10.4081/cardiogenetics.2013.e9

By:

Palladino, Alberto;
Nigro, Gerardo;
Politano, Luisa

Publication type:

Article

Cardiovascular magnetic resonance in rare systemic diseases.

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 44, doi. 10.4081/cardiogenetics.2013.e8

By:

D'Andrea, Antonello;
Fontana, Marianna;
Cocchia, Rosangela;
Calabrò, Raffaele;
Russo, Maria Giovanna;
Moon, James C.

Publication type:

Article

High-density lipoprotein-cholesterol, reverse cholesterol transport, and cardiovascular risk: a tale of genetics?

Published in:

Cardiogenetics, 2013, v. 3, n. 1, p. 38, doi. 10.4081/cardiogenetics.2013.e7

By:

Cimmino, Giovanni;
D'Amico, Chiara;
Ciccarelli, Giovanni;
Golino, Marco;
Morello, Alberto;
D'Elia, Saverio;
Marchese, Valeria;
Golino, Paolo

Publication type:

Article