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The role of rehabilitation in the management of late-onset Pompe disease: a narrative review of the level of evidence

Giovanni Iolascon ¹, Michele Vitacca ², Elena Carraro ³, Carmelo Chisari ⁴, Pietro Fiore ⁵, Sonia Messina ⁶, Tiziana Enrica Giovanna Mongini ⁷, Valeria A. Sansone ⁸, Antonio Toscano ⁹ and Gabriele Siciliano ¹⁰, on behalf of AIM (Italian Association of Myology), AIPO (Italian Association of Hospital Pulmonologists), SIRN (Italian Society of Neurorehabilitation), and SIMFER (Italian Society of Physical Medicine and Rehabilitation)

Metabolic impairments in patients with myotonic dystrophy type 2

Milorad Vujnic ¹, Stojan Peric ², Zeljka Calic ³, Natasa Benovic ², Tanja Nisic ⁴, Jovan Pesovic ⁵, Dusanka Savic-Pavicevic ⁵ and Vidosava Rakocevic-Stojanovic ²

mmune-mediated necrotizing myopathy due to statins exposure

Luisa Villa ^{1 2}, Alberto Lerario ¹, Sonia Calloni ³, Lorenzo Peverelli ¹, Caterina Matinato ⁴, Federica de Liso ⁴, Ferruccio Ceriotti ⁴, Roberto Tironi ¹, Monica Sciacco ¹, Maurizio Moggio ¹, Fabio Triulzi ³ and Claudia Cinnante ³

Novel desmoplakin mutations in familial Carvajal syndrome

Danat Yermakovich ¹, Larysa Sivitskaya ¹, Tatiyana Vaikhanskaya ², Nina Danilenko ¹ and Iryna Motuk ³

Heart transplantation in a patient with Myotonic Dystrophy type 1 and end-stage dilated cardiomyopathy: a short term follow-up

Andrea Antonio Papa ¹, Federica Verrillo ¹, Marianna Scutifero ², Anna Rago ¹, Salvatore Morra ², Antonio Cassese ¹, Nadia Della Cioppa ³, Maria Cristina Giada Magliocca ⁴, Dario Galante ⁵, Alberto Palladino ², Paolo Golino ¹ and Luisa Politano ²

Therapeutic approach with Ataluren in Duchenne symptomatic carriers with nonsense mutations in dystrophin gene. Results of a 9-month follow-up in a case report

Paola D’Ambrosio ¹, Chiara Orsini ¹, Vincenzo Nigro ² and Luisa Politano ¹

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