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JAMA Network Open|May 2, 2020
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular DystrophyLucia Ruggiero, Fabiano Mele, Fiore Manganelli, et al.Journal of Neurology|April 30, 2016
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypesGiulia Ricci, Lucia Ruggiero, Liliana Vercelli, et al.BMJ Open|January 7, 2016
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National RegistryAna Nikolic, Giulia Ricci, Francesco Sera, et al.Scientific Reports|December 11, 2020
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosisGiulia Ricci, Fabiano Mele, Monica Govi, et al.Journal of Neuromuscular Diseases|March 29, 2026
Real-world effectiveness and safety of zilucoplan in patients with anti-AChR myasthenia gravis: A retrospective cohort study in FranceGiulia Tammam, Abderhmane Slioui, Diane Friedman, et al.Orphanet Journal of Rare Diseases|September 2, 2025
Prevalence and predictors of uncommon features in FSHD1 patients: insights from the French FSHD registryBenoît Sanson, Abderhmane Slioui, Jérémy Garcia, et al.International Journal of Molecular Sciences|April 16, 2020
Interpretation of the Epigenetic Signature of Facioscapulohumeral Muscular Dystrophy in Light of Genotype-Phenotype StudiesAna Nikolic, Takako I Jones, Monica Govi, et al.The Lancet. Oncology|May 1, 2013
Planning cancer control in Latin America and the CaribbeanPaul E Goss, Brittany L Lee, Tanja Badovinac-Crnjevic, et al.Pageof 6