X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (809) 809
Book Chapter (42) 42
Book / eBook (7) 7
Publication (6) 6
Conference Proceeding (3) 3
Patent (2) 2
Web Resource (2) 2
Book Review (1) 1
Magazine Article (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (444) 444
cardiac & cardiovascular systems (262) 262
male (257) 257
female (254) 254
child (194) 194
adolescent (166) 166
cardiomyopathy (161) 161
mutation (147) 147
adult (146) 146
pediatrics (131) 131
child, preschool (130) 130
infant (116) 116
cardiovascular (96) 96
electrocardiography (90) 90
risk factors (88) 88
children (86) 86
heart (85) 85
heart failure (82) 82
peripheral vascular disease (75) 75
cardiology (74) 74
genetics (74) 74
phenotype (73) 73
abridged index medicus (71) 71
diagnosis (70) 70
animals (69) 69
infant, newborn (66) 66
heart diseases (65) 65
mutations (65) 65
dilated cardiomyopathy (63) 63
disease (63) 63
genetic aspects (63) 63
long qt syndrome - genetics (63) 63
gene (60) 60
genotype (60) 60
genetics & heredity (59) 59
middle aged (57) 57
health aspects (55) 55
echocardiography (54) 54
retrospective studies (54) 54
transplantation (54) 54
research (48) 48
cardiology and cardiovascular medicine (47) 47
mortality (47) 47
internal medicine (46) 46
pedigree (46) 46
arrhythmia (45) 45
hematology (44) 44
long-qt syndrome (42) 42
cardiomyopathy, dilated - genetics (41) 41
long qt syndrome (40) 40
death, sudden, cardiac - etiology (39) 39
polymerase chain reaction (39) 39
care and treatment (38) 38
genes (38) 38
medical colleges (38) 38
heart transplantation (37) 37
hypertrophic cardiomyopathy (37) 37
registries (37) 37
prognosis (36) 36
sudden cardiac death (36) 36
dna mutational analysis (35) 35
myocardium - pathology (35) 35
analysis (33) 33
follow-up studies (33) 33
mice (33) 33
sodium channels - genetics (33) 33
long qt syndrome - physiopathology (32) 32
molecular sequence data (32) 32
age (31) 31
biopsy (31) 31
proteins (31) 31
aged (30) 30
biochemistry & molecular biology (30) 30
diseases (28) 28
epidemiology (28) 28
myocarditis (28) 28
nav1.5 voltage-gated sodium channel (28) 28
prospective studies (28) 28
genetic predisposition to disease (27) 27
syndrome (27) 27
treatment outcome (27) 27
cardiomyopathies - genetics (26) 26
surgery (26) 26
cardiovascular diseases (25) 25
expression (25) 25
heart attacks (25) 25
incidence (25) 25
medicine, research & experimental (25) 25
young adult (25) 25
cardiomyopathy, hypertrophic - genetics (24) 24
chromosome mapping (24) 24
gene mutations (24) 24
heart-failure (24) 24
medicine, general & internal (24) 24
myocardium (24) 24
proportional hazards models (24) 24
arrhythmias (23) 23
congenital heart disease (23) 23
genetic testing (23) 23
united states (23) 23
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


Journal of the American College of Cardiology, ISSN 0735-1097, 2010, Volume 55, Issue 6, pp. 587 - 597
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 2013, Volume 62, Issue 23, pp. 2155 - 2166
Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart defect. We explore “hot topics” to highlight areas of emerging science for clinicians... 
Cardiovascular | Internal Medicine | ventricular function and heart failure | pulmonary regurgitation | arrhythmias | sudden cardiac death | pulmonary valve replacement | tetralogy of Fallot | imaging | SURGICALLY REPAIRED TETRALOGY | CARDIAC & CARDIOVASCULAR SYSTEMS | CARDIOVASCULAR MAGNETIC-RESONANCE | FOLLOW-UP | CARDIOPULMONARY EXERCISE | RADIOFREQUENCY CATHETER ABLATION | PULMONARY VALVE-REPLACEMENT | CONGENITAL HEART-DISEASE | RIGHT-VENTRICULAR FUNCTION | IMPLANTABLE CARDIOVERTER-DEFIBRILLATORS | Pulmonary Valve Insufficiency - physiopathology | Heart Valve Prosthesis Implantation | Death, Sudden, Cardiac - epidemiology | Humans | Heart Failure - physiopathology | Tachycardia, Atrioventricular Nodal Reentry - mortality | Ventricular Dysfunction, Left - complications | Death, Sudden, Cardiac - etiology | Pulmonary Valve Insufficiency - etiology | Heart Failure - therapy | Cardiac Catheterization | Defibrillators, Implantable | Tetralogy of Fallot - diagnosis | Heart Failure - etiology | Infant, Newborn | Catheters, Indwelling | Tetralogy of Fallot - pathology | Reoperation | Echocardiography | Tachycardia, Ventricular - etiology | Ventricular Dysfunction, Left - etiology | Tetralogy of Fallot - genetics | Tetralogy of Fallot - therapy | Magnetic Resonance Imaging | Tachycardia, Ventricular - mortality | Tachycardia, Atrioventricular Nodal Reentry - etiology | Tetralogy of Fallot - surgery | Cardiac Surgical Procedures - methods | Pulmonary Valve Insufficiency - surgery | Tetralogy of Fallot - physiopathology | Palliative Care - methods | Tetralogy of Fallot - complications | Tetralogy of Fallot | Heart | Genetic disorders | Arrhythmia | Therapeutics | Valves | Homeopathy | Materia medica and therapeutics | Cardiac arrhythmia | Heart attacks | Mutation | Cardiology | Chromosomes | Mortality
Journal Article
The Lancet (British edition), ISSN 0140-6736, 2015, Volume 386, Issue 9995, pp. 813 - 825
Summary Left ventricular non-compaction, the most recently classified form of cardiomyopathy, is characterised by abnormal trabeculations in the left... 
Internal Medicine | MEDICINE, GENERAL & INTERNAL | PRACTICE GUIDELINES | CONGENITAL HEART-DISEASE | ISOLATED NONCOMPACTION | AMERICAN-COLLEGE | ASSOCIATION TASK-FORCE | BARTH-SYNDROME | LONG QT SYNDROME | TERM CLINICAL-COURSE | TRANSCRIPTION FACTOR | SPONGY MYOCARDIUM | Cardiomyopathy, Dilated - classification | Echocardiography | Isolated Noncompaction of the Ventricular Myocardium - therapy | Humans | Isolated Noncompaction of the Ventricular Myocardium - classification | Magnetic Resonance Angiography | Anticoagulants - therapeutic use | Male | Treatment Outcome | Arrhythmias, Cardiac - etiology | Signal Transduction - genetics | Mutation - genetics | Animals | Defibrillators, Implantable | Electrocardiography | Cardiomyopathy, Dilated - diagnosis | Female | Mice | Cardiomyopathy, Dilated - therapy | Disease Models, Animal | Isolated Noncompaction of the Ventricular Myocardium - diagnosis | Heart failure | Heart | Genetic disorders | Cardiomyopathy | Heart diseases | Jaw | Regulators | Embryo cells | Elastic scattering | Infants | Biochemistry | Compaction | Incidence | Proteins | Signal transduction | Diagnosis | Cardiac muscle | Abnormalities | Fetuses | Benign | Recesses | Endothelium | Blood circulation | Morphology | Stem cells | Myocardium | Death | Adults | Notch protein | Cardiovascular diseases | Cardiac arrhythmia | Calcineurin | Risk | Valves | Chin | Transplantation | Defects | Morphogenesis | Children | Cardiology | Ultrasound | Age | Stroke | Health risks | Septum | Ribonucleic acid--RNA | Catheters | Solidification | Magnetic resonance imaging | Ventricle | Methylation | Differentiation
Journal Article
The Lancet (British edition), ISSN 0140-6736, 2010, Volume 375, Issue 9716, pp. 752 - 762
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2014, Volume 64, Issue 25, pp. 2765 - 2776
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 2009, Volume 54, Issue 3, pp. 250 - 254
Journal Article
Journal of Heart and Lung Transplantation, ISSN 1053-2498, 2010, Volume 29, Issue 8, pp. 914 - 956
Journal Article