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European Journal of Heart Failure|January 25, 2020
Carpal tunnel syndrome in cardiac amyloidosis: implications for early diagnosis and prognostic role across the spectrum of aetiologiesAgnese Milandri, Andrea Farioli, Christian Gagliardi, et al.
JACC. Cardiovascular Imaging|June 18, 2011
Role of (99m)Tc-DPD scintigraphy in diagnosis and prognosis of hereditary transthyretin-related cardiac amyloidosisClaudio Rapezzi, Candida C Quarta, Pier Luigi Guidalotti, et al.
Journal of the American College of Cardiology|August 20, 2011
Diagnostic work-up and risk stratification in X-linked dilated cardiomyopathies caused by dystrophin defectsMarta Diegoli, Maurizia Grasso, Valentina Favalli, et al.
Frontiers in Physiology|November 8, 2021
Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic DiseasesMaria Sofia Falzarano, Rachele Rossi, Andrea Grilli, et al.
Biomed Research International|January 7, 2014
Biodistribution and molecular studies on orally administered nanoparticle-AON complexes encapsulated with alginate aiming at inducing dystrophin rescue in mdx miceMaria Sofia Falzarano, Chiara Passarelli, Elena Bassi, et al.
Stem Cell Reports|October 31, 2025
Modulation of the JAK2-STAT3 pathway promotes expansion and maturation of human iPSC-derived myogenic progenitor cellsLuca Caputo, Cedomir Stamenkovic, Matthew T Tierney, et al.
Human Mutation|March 1, 2021
A single NGS-based assay covering the entire genomic sequence of the DMD gene facilitates diagnostic and newborn screening confirmatory testingBabi R R Nallamilli, Alka Chaubey, C A Valencia, et al.
Molecular and Cellular Neurosciences|July 2, 2017
A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctionsPaola Imbrici, Concetta Altamura, Francesca Gualandi, et al.
Heart Rhythm|March 11, 2024
Cardiac conduction disorders in young adults: Clinical characteristics and genetic background of an underestimated populationCristina Balla, Alice Margutti, Beatrice De Carolis, et al.
Human Gene Therapy|August 18, 2016
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and PhenotypeMaria Sofia Falzarano, Domenico D'Amario, Andrea Siracusano, et al.
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