Unraveling of the innate immune system and the complement activation in FSHD cellular muscle models towards the identification of disease biomarkers

Patient-derived organoids as a new in vitro paradigm to study Myotonic Dystrophy type 1

Fragility fractures prevalence and bone health in a large cohort of untreated SMA patients

Subjective assessment of sleep quality in adult patients with dystrophinopathy: a single centre experience.

Nonsense mutations in Becker muscular dystrophy: DMD gene position and disease severity

A comprehensive evaluation of mobile health technology revealed the ability to identify subtle motor impairment in patients with mild and asymptomatic Pompe disease: one-year follow-up.

Kaposi’s sarcoma in myasthenia gravis patient in oral steroids treatment: two case report

The hidden face of Duchenne (Neuro)Muscular Dystrophy: social cognition impairment as a feature of the neuropsychological phenotype of DMD

Differences in clinical severity according to MG ADL score in patients with Myasthenia Gravis.