Guidelines for the Diagnosis and Management of Hypertrophic Cardiomyopathy
Author:
Publisher
Elsevier BV
Subject
Cardiology and Cardiovascular Medicine,Pulmonary and Respiratory Medicine
Reference6 articles.
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2. Compound and double mutations in hypertrophic cardiomyopathy patients: implications for genetic testing and counselling;Ingles;J Med Genet,2005
3. Multiple mutations in genetic cardiovascular disease: a marker of disease severity?;Kelly;Circ Cardiovasc Genet,2009
4. The genetic basis of hypertrophic cardiomyopathy;Lind;Exp Rev Cardiovasc Ther,2006
5. Prevention of sudden cardiac death and selection of patients for implantable cardioverter-defibrillators in hypertrophic cardiomyopathy;Maron;JAMA,2007
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1. Longitudinal Psychometric Analysis of the Hypertrophic Cardiomyopathy Symptom Questionnaire (HCMSQ) Using Outcomes from the Phase III EXPLORER-HCM Trial;PharmacoEconomics - Open;2022-06-20
2. Development of the Hypertrophic Cardiomyopathy Symptom Questionnaire (HCMSQ): A New Patient-Reported Outcome (PRO) Instrument;PharmacoEconomics - Open;2022-06-02
3. Patient experiences with hypertrophic cardiomyopathy: a conceptual model of symptoms and impacts on quality of life;Journal of Patient-Reported Outcomes;2020-12
4. Next-generation sequencing (NGS) as a molecular diagnostic tool for hypertrophic cardiomyopathy in a Chinese boy due to novel compound heterozygous mutations in the MYBPC3 gene;Medicine;2019-03
5. Role of the Cardiac Pathologist in Evaluating Sudden Natural Deaths;Multidisciplinary Medico-Legal Death Investigation;2018
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