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151. Syncope in hypertrophic cardiomyopathy (part II): An expert consensus statement on the diagnosis and management

155. European Society of Cardiology

160. Integrin α7 Mutations Are Associated With Adult‐Onset Cardiac Dysfunction in Humans and Mice

162. Cardiac Outcomes in Adults With Mitochondrial Diseases

164. Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry

165. Colaboradores

168. International External Validation Study of the 2014 European Society of Cardiology Guidelines on Sudden Cardiac Death Prevention in Hypertrophic Cardiomyopathy (EVIDENCE-HCM)

171. Improving Interpretation of Cardiac Phenotypes and Enhancing Discovery With Expanded Knowledge in the Gene Ontology

173. ADVANCES IN HEART FAILURE, MECHANICAL CIRCULATORY SUPPORT AND TRANSPLANT.

175. Alpha kinase 3 signaling at the M-band maintains sarcomere integrity and proteostasis in striated muscle

178. Takotsubo Cardiomyopathy: Do the Genetics Matter?

181. The European Heart Journal: fulfilling the mission

182. Indications and utility of cardiac genetic testing in athletes

183. Cardiac Outcomes in Adults With Mitochondrial Diseases

184. The European Heart Journal:fulfilling the mission

185. Interpretation and actionability of genetic variants in cardiomyopathies:a position statement from the European Society of Cardiology Council on cardiovascular genomics

186. 2021 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy:Developed by the Task Force on cardiac pacing and cardiac resynchronization therapy of the European Society of Cardiology (ESC) With the special contribution of the European Heart Rhythm Association (EHRA)

187. Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics

193. Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator

195. Clinical Features and Natural History of Preadolescent Nonsyndromic Hypertrophic Cardiomyopathy

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