Deep basal inferoseptal crypts occur more commonly in patients with hypertrophic cardiomyopathy due to disease-causing myofilament mutations

Radiology

Volumn 269, Issue 1, 2013, Pages 68-76

  Deva, Djeven Parameshvara ^a   Williams, Lynne K ^a   Care, Melanie ^b   Siminovitch, Katherine A ^b   Moshonov, Hadas ^a   Wintersperger, Bernd Juergen ^a,c   Rakowski, Harry ^a   Crean, Andrew Michael ^a  

^a UNIVERSITY OF TORONTO   (Canada)

^b UNIVERSITY HEALTH NETWORK   (Canada)

^c LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CARDIOVASCULAR MAGNETIC RESONANCE; COHORT ANALYSIS; CONTRAST ENHANCEMENT; CONTROLLED STUDY; DEEP BASAL INFEROSEPTAL CRYPT; FEMALE; GENETIC SCREENING; GENOTYPE; HUMAN; HYPERTENSION; HYPERTROPHIC CARDIOMYOPATHY; IMAGE ANALYSIS; INFORMED CONSENT; MAJOR CLINICAL STUDY; MALE; MYOFILAMENT; NUCLEAR MAGNETIC RESONANCE SCANNER; PHENOTYPE; PREDICTIVE VALUE; PREDICTOR VARIABLE; PRIORITY JOURNAL; RETROSPECTIVE STUDY;

CARDIAC MYOSINS; CARDIOMYOPATHY, HYPERTROPHIC; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEART SEPTUM; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MYOSIN HEAVY CHAINS; ONTARIO; POLYMORPHISM, SINGLE NUCLEOTIDE; PREVALENCE; RISK FACTORS;

EID: 84884693419     PISSN: 00338419     EISSN: 15271315     Source Type: Journal    
DOI: 10.1148/radiol.13122344     Document Type: Article

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