Autori: Frosini S*

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KLHL40-Related Myopathy: A Systematic Review and Insight into a Follow-up Biomarker via a New Case Report.

Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study

Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature.

Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?

Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal data

Learning disabilities in neuromuscular disorders: a springboard for adult life.

Infantile-Onset Pompe Disease: The Care Beyond the Cure.

Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational Study

The 6 minute walk test and performance of upper limb in ambulant duchenne muscular dystrophy boys

Benefits of glucocorticoids in non-ambulant boys/men with Duchenne muscular dystrophy: A multicentric longitudinal study using the Performance of Upper Limb test

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