Autori: Di Bari A

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Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1-Results from a Retrospective Analysis in Italy

Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity

Assessing Prevalence and Characteristics of Oro-bulbar Involvement in Children and Adults with SMA Type 2 and 3 Using a Multimodal Approach

Respiratory Needs in Patients with Type 1 Spinal Muscular Atrophy Treated with Nusinersen

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