Paola Melacini
Padova, Italy
Last Updated: 09/26/2026
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Found 11 publications
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy.
Journal: Journal of neuromuscular diseases
Published: February 16, 2024
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies.
Journal: Journal of clinical medicine
Published: February 27, 2021
Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive Physiology.
Journal: Circulation. Genomic and precision medicine
Published: February 01, 2020
Co-inheritance of mutations associated with arrhythmogenic cardiomyopathy and hypertrophic cardiomyopathy.
Journal: European journal of human genetics : EJHG
Published: February 20, 2017
Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy.
Journal: PloS one
Published: July 14, 2015
Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies.
Journal: Archives of medical science : AMS
Published: February 04, 2015
A founder MYBPC3 mutation results in HCM with a high risk of sudden death after the fourth decade of life.
Journal: Journal of medical genetics
Published: December 01, 2014
Prevalence and clinical meaning of isolated increase of QRS voltages in hypertrophic cardiomyopathy versus athlete's heart: relevance to athletic screening.
Journal: International journal of cardiology
Published: May 22, 2013
Pilot trial of clenbuterol in spinal and bulbar muscular atrophy.
Journal: Neurology
Published: May 07, 2013
No evidence of cardiomyopathy in spinal and bulbar muscular atrophy.
Journal: Acta neurologica Scandinavica
Published: April 09, 2013
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy.
Journal: European journal of human genetics : EJHG
Published: May 03, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026