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One or more keywords matched the following items that are connected to MacRae, Calum
Item TypeName
Academic Article Genetic screening and risk assessment in hypertrophic cardiomyopathy.
Academic Article Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.
Academic Article Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.
Academic Article The genetics of hypertrophic cardiomyopathy
Academic Article Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.
Academic Article Clinical screening and genetic testing.
Academic Article Independent origin of myosin mutations in hypertrophic cardiomyopathy
Academic Article The genetics of hypertrophic cardiomyopathy
Academic Article A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.
Academic Article Electrophysiologic characteristics of accessory atrioventricular connections in an inherited form of Wolff-Parkinson-White syndrome.
Academic Article Subclinical myocardial damage revealed by CK-MB2 isoform release in hypertrophic cardiomyopathy
Academic Article Mode of action of cardiac troponin T mutations in familial hypertrophic cardiomyopathy
Academic Article Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish.
Academic Article Clinical implications of cardiac troponin T mutations that cause familial hypertrophic cardiomyopathy
Academic Article In vivo natriuretic peptide reporter assay identifies chemical modifiers of hypertrophic cardiomyopathy signalling.
Academic Article A dinucleotide repeat polymorphism in the MYBPH gene.
Academic Article Management strategy in 249 consecutive patients with obstructive hypertrophic cardiomyopathy referred to a dedicated program.
Academic Article An evaluation of ribonuclease protection assays for the detection of beta-cardiac myosin heavy chain gene mutations.
Academic Article Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
Academic Article Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.
Academic Article A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.
Concept Cardiomyopathy, Hypertrophic
Academic Article Revisiting risk stratification in hypertrophic cardiomyopathy: do we need to start from scratch?
Academic Article Comparison of echocardiographic and cardiac magnetic resonance imaging in hypertrophic cardiomyopathy sarcomere mutation carriers without left ventricular hypertrophy.
Academic Article Mendelian forms of structural cardiovascular disease.
Academic Article The Design of the Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Trial.
Academic Article A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients.
Academic Article The uptake of family screening in hypertrophic cardiomyopathy and an online video intervention to facilitate family communication.
Academic Article Baseline Characteristics of the VANISH Cohort.
Search Criteria
  • Hypertrophic Cardiomyopathy
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.