Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy

Journal of the American College of Cardiology

Volumn 71, Issue 7, 2018, Pages 711-722

  van Waning, Jaap I ^a   Caliskan, Kadir ^a   Hoedemaekers, Yvonne M ^b   van Spaendonck Zwarts, Karin Y ^c   Baas, Annette F ^d   Boekholdt, S Matthijs ^c   van Melle, Joost P ^b   Teske, Arco J ^d   Asselbergs, Folkert W ^d   Backx, Ad P C M ^c   du Marchie Sarvaas, Gideon J ^b   Dalinghaus, Michiel ^a   Breur, Johannes M P J ^d   Linschoten, Marijke P M ^d   Verlooij, Laura A ^b   Kardys, Isabella ^a   Dooijes, Dennis ^d   Lekanne Deprez, Ronald H ^c   IJpma, Arne S ^a   van den Berg, Maarten P ^b   Hofstra, Robert M W ^a   van Slegtenhorst, Marjon A ^a   Jongbloed, Jan D H ^b   Majoor Krakauer, Danielle ^a   more..

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

^d UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

Author keywords

genetics; LVNC; noncompaction cardiomyopathy; outcome; prognosis

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; ATRIAL FIBRILLATION; BICUSPID AORTIC VALVE; BRAIN ISCHEMIA; CARDIOVASCULAR RISK; CEREBROVASCULAR ACCIDENT; CHILD; CLINICAL FEATURE; CLINICAL OUTCOME; CONGENITAL HEART DISEASE; CONGESTIVE CARDIOMYOPATHY; EBSTEIN ANOMALY; FEMALE; FOLLOW UP; GENE; GENE MUTATION; GENE STRUCTURE; GENETIC ASSOCIATION; GENETIC CORRELATION; GENETIC HETEROGENEITY; GENOTYPE; HEART ARREST; HEART ATRIUM SEPTUM DEFECT; HEART FAILURE; HEART LEFT BUNDLE BRANCH BLOCK; HEART RIGHT VENTRICLE FAILURE; HEART TRANSPLANTATION; HEART VALVE REPLACEMENT; HEART VENTRICLE FIBRILLATION; HEART VENTRICLE SEPTUM DEFECT; HEART VENTRICLE TACHYCARDIA; HEMOCHROMATOSIS; HEREDITARY HYPERTENSION; HETEROZYGOTE; HIGH RISK PATIENT; HUMAN; HYPERTENSION; HYPERTROPHIC CARDIOMYOPATHY; INFANT; KIDNEY INFARCTION; LEFT VENTRICULAR SYSTOLIC DYSFUNCTION; MAJOR ADVERSE CARDIAC EVENT; MAJOR CLINICAL STUDY; MALE; MESENTERIC BLOOD VESSEL OCCLUSION; MYBPC3 GENE; MYH7 GENE; NEWBORN; PREDICTION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SUDDEN CARDIAC DEATH; THROMBOEMBOLISM; TRANSIENT ISCHEMIC ATTACK; TTN GENE; VENTRICULAR NONCOMPACTION; CLINICAL TRIAL; GENETICS; MIDDLE AGED; MULTICENTER STUDY; MUTATION; NETHERLANDS; PRESCHOOL CHILD; TIME FACTOR; TREATMENT OUTCOME; YOUNG ADULT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; DEATH, SUDDEN, CARDIAC; FEMALE; FOLLOW-UP STUDIES; HUMANS; INFANT; INFANT, NEWBORN; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; MALE; MIDDLE AGED; MUTATION; NETHERLANDS; RETROSPECTIVE STUDIES; TIME FACTORS; TREATMENT OUTCOME; YOUNG ADULT;

EID: 85044372680     PISSN: 07351097     EISSN: 15583597     Source Type: Journal    
DOI: 10.1016/j.jacc.2017.12.019     Document Type: Article

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