S. Tripodi

Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis

F. Sera, L. Santoro, C. Angelini, 2020, Scientific Reports.

A 5-year clinical follow-up study from the Italian National Registry for FSHD

F. Sera, L. Santoro, C. Angelini, 2020, Journal of Neurology.

Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy

L. Santoro, D. Bruzzese, C. Angelini, 2020, JAMA network open.