Cinzia Bettio

Counseling and prenatal diagnosis in facioscapulohumeral muscular dystrophy: A retrospective study on a 13‐year multidisciplinary approach

R. Tupler, V. Salsi, E. Bertucci, 2022, Health science reports.

The Italian National Registry for FSHD: an enhanced data integration and an analytics framework towards Smart Health Care and Precision Medicine for a rare disease

Sonia Bergamaschi, Luca Gagliardelli, Mirko Orsini, 2021, Orphanet Journal of Rare Diseases.

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.

Increased resistance towards fatigability in patients with facioscapulohumeral muscular dystrophy

G. Siciliano, G. D’Antona, R. Tupler, 2021, European Journal of Applied Physiology.