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You searched for: Author/Creator Crotti, Lia

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1. 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease. (31st May 2014)

2. 465 Unmasking the prevalence of cardiac amyloidosis in the real world: first insights from the phase 2 of active study, an Italian nationwide survey. (8th December 2021)

3. 517 RIGHT ATRIAL THROMBUS IN A PATIENT WITH CARDIAC AMYLOIDOSIS: A MULTIMODALITY IMAGING APPROACH. (15th December 2022)

4. 663 OCCURRENCE OF VENTRICULAR AND SUPRAVENTRICULAR ARRHYTHMIAS IN BRUGADA SYNDROME: RESULTS OF A TERTIARY REFERRAL CENTER EXPERIENCE. (15th December 2022)

5. 813 The added value of transthoracic three dimensional echocardiography in apical hypertrophic cardiomyopathy. (8th December 2021)

6. A national survey on prevalence of possible echocardiographic red flags of amyloid cardiomyopathy in consecutive patients undergoing routine echocardiography: study design and patients characterization — the first insight from the AC-TIVE Study. (9th September 2021)

9. Cadherin 2-Related Arrhythmogenic Cardiomyopathy: Prevalence and Clinical Features. (10th February 2021)

10. Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry. (6th June 2019)