X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (42) 42
male (34) 34
index medicus (33) 33
female (31) 31
cardiac & cardiovascular systems (27) 27
middle aged (26) 26
life sciences (21) 21
aged (17) 17
adult (14) 14
diagnosis (13) 13
human health and pathology (12) 12
cardiology and cardiovascular system (10) 10
risk factors (10) 10
echocardiography (9) 9
france - epidemiology (9) 9
prevalence (9) 9
prospective studies (9) 9
treatment outcome (9) 9
aged, 80 and over (8) 8
heart failure (8) 8
mortality (8) 8
prognosis (8) 8
heart failure - physiopathology (7) 7
infectious diseases (7) 7
echocardiography, transesophageal (6) 6
genetics & heredity (6) 6
guidelines (6) 6
severity of illness index (6) 6
[ sdv.mhep.csc ] life sciences [q-bio]/human health and pathology/cardiology and cardiovascular system (5) 5
[sdv.mhep.csc]life sciences [q-bio]/human health and pathology/cardiology and cardiovascular system (5) 5
disease (5) 5
electrocardiography (5) 5
endocarditis, bacterial - microbiology (5) 5
exercise (5) 5
france (5) 5
genetics (5) 5
hypertrophic cardiomyopathy (5) 5
microbiology (5) 5
mutation (5) 5
staphylococcus aureus (5) 5
[ sdv ] life sciences [q-bio] (4) 4
analysis (4) 4
bioengineering (4) 4
cardiology (4) 4
cardiomyopathy (4) 4
care and treatment (4) 4
classification (4) 4
cohort studies (4) 4
computer science (4) 4
genetic aspects (4) 4
heart failure - rehabilitation (4) 4
heart valve diseases - diagnostic imaging (4) 4
magnetic resonance imaging (4) 4
microbiology and parasitology (4) 4
muscle, skeletal - physiology (4) 4
population (4) 4
preserved ejection fraction (4) 4
registries (4) 4
risk-factors (4) 4
skeletal-muscle (4) 4
stroke (4) 4
acute renal failure (3) 3
adolescent (3) 3
association (3) 3
bacteremia (3) 3
biomarkers - blood (3) 3
calcinosis - diagnostic imaging (3) 3
cardiomyopathy, hypertrophic - genetics (3) 3
cardiovascular system (3) 3
carvedilol (3) 3
chronic disease (3) 3
electric stimulation therapy (3) 3
european-society (3) 3
exercise tolerance - physiology (3) 3
fibrillation (3) 3
follow-up studies (3) 3
genetic counseling (3) 3
genetic research (3) 3
genotype (3) 3
heart (3) 3
heart failure - complications (3) 3
heart failure - epidemiology (3) 3
heart failure - therapy (3) 3
heart failure with preserved ejection fraction (3) 3
heart rate - physiology (3) 3
hemodynamics (3) 3
implantation (3) 3
infective endocarditis (3) 3
management (3) 3
mitral valve - diagnostic imaging (3) 3
outcomes (3) 3
oxygen consumption (3) 3
pacemaker (3) 3
patent foramen ovale (3) 3
patients (3) 3
phenotype (3) 3
physiological aspects (3) 3
predictors (3) 3
quality of life (3) 3
renal infarction (3) 3
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The New England Journal of Medicine, ISSN 0028-4793, 09/2017, Volume 377, Issue 11, pp. 1011 - 1021
Journal Article
by Auffret, Vincent and Lefevre, Thierry and Van Belle, Eric and Eltchaninoff, Hélène and Iung, Bernard and Koning, René and Motreff, Pascal and Leprince, Pascal and Verhoye, Jean Philippe and Manigold, Thibaut and Souteyrand, Geraud and Boulmier, Dominique and Joly, Patrick and Pinaud, Frédéric and Himbert, Dominique and Collet, Jean Philippe and Rioufol, Gilles and Ghostine, Said and Bar, Olivier and Dibie, Alain and Champagnac, Didier and Leroux, Lionel and Collet, Frédéric and Teiger, Emmanuel and Darremont, Olivier and Folliguet, Thierry and Leclercq, Florence and Lhermusier, Thibault and Olhmann, Patrick and Huret, Bruno and Lorgis, Luc and Drogoul, Laurent and Bertrand, Bernard and Spaulding, Christian and Quilliet, Laurent and Cuisset, Thomas and Delomez, Maxence and Beygui, Farzin and Claudel, Jean-Philippe and Hepp, Alain and Jegou, Arnaud and Gommeaux, Antoine and Mirode, Anfani and Christiaens, Luc and Christophe, Charles and Cassat, Claude and Metz, Damien and Mangin, Lionel and Isaaz, Karl and Jacquemin, Laurent and Guyon, Philippe and Pouillot, Christophe and Makowski, Serge and Bataille, Vincent and Rodés-Cabau, Josep and Gilard, Martine and Le Breton, Hervé and Le Breton, Hervé and Eltchaninoff, Hélène and Gilard, Martine and Iung, Bernard and Le Breton, Hervé and Lefevre, Thierry and Van Belle, Eric and Laskar, Marc and Leprince, Pascal and Iung, Bernard and Bataille, Vincent and Chevalier, Bernard and Garot, Philippe and Hovasse, Thomas and Lefevre, Thierry and Donzeau Gouge, Patrick and Farge, Arnaud and Romano, Mauro and Cormier, Bertrand and Bouvier, Erik and Bauchart, Jean-Jacques and Bodart, Jean-Christophe and Delhaye, Cédric and Houpe, David and Lallemant, Robert and Leroy, Fabrice and Sudre, Arnaud and Van Belle, Eric and Juthier, Francis and Koussa, Mohamed and Modine, Thomas and Rousse, Natacha and Auffray, Jean-Luc and Richardson, Marjorie and Berland, Jacques and Eltchaninoff, Hélène and Godin, Mathieu and Koning, René and Bessou, Jean-Paul and Letocart, Vincent and Manigold, Thibaut and Roussel, Jean-Christian and Jaafar, Philippe and ... and FRANCE TAVI Investigators
Journal of the American College of Cardiology, ISSN 0735-1097, 07/2017, Volume 70, Issue 1, pp. 42 - 55
Journal Article
European Journal of Heart Failure, ISSN 1388-9842, 02/2011, Volume 13, Issue 2, pp. 177 - 185
Journal Article
Journal Article
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2017, Volume 173, Issue 2, pp. 531 - 536
Journal Article
Journal Article
European Journal of Heart Failure, ISSN 1388-9842, 04/2013, Volume 15, Issue 4, pp. 465 - 476
Journal Article
Human Mutation, ISSN 1059-7794, 02/2020, Volume 41, Issue 2, pp. 465 - 475
Hypertrophic cardiomyopathy (HCM) is the most common heritable cardiomyopathy, historically believed to affect 1 of 500 people. MYBPC3 pathogenic variations... 
minigene reporter assay | hypertrophic cardiomyopathy | splicing | Next‐generation sequencing | intronic variation | Next-generation sequencing | GENE | GENETICS & HEREDITY | TOOL | Diagnosis | Mutation | Variation | Cardiomyopathy | Nonsense mutation
Journal Article
Journal Article