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AUTOMA: a wearable device to assess the upper limb muscular activity in patients with neuromuscular disorders

Mario Milazzo ^{1 *}, Andrea Spezzaneve ^{1 *}, Guja Astrea ², Francesca Giorgolo ³, Alessandro Tonacci ⁴, Francesco Sansone ⁴, Marco Calderisi ³, the Ingene Group, Raffaele Conte ⁴, Filippo M. Santorelli ², Stefano Roccella ¹
DOI 10.36185/2532-1900-057

Can symptomatic nmDuchenne carriers benefit from treatment with ataluren? Results of 193-month follow-up

Amir Dori ¹, Michela Guglieri ², Marianna Scutifero ³, Luigia Passamano ³, Antonio Trabacca ⁴, Luisa Politano ^3,5
DOI 10.36185/2532-1900-058

Magnetic resonance imaging pattern variability in dysferlinopathy

Sergey N. Bardakov ¹, Vadim A. Tsargush ¹, Pierre G. Carlier ², Sergey S. Nikitin ³, Sergey A. Kurbatov ^4,5, Angelina A. Titova ⁶, Zoya R. Umakhanova ⁷, Patimat G. Akhmedova ⁷, Raisat M. Magomedova ⁷, Igor S. Zheleznyak ¹, Alexander A. Emelyantsev ¹, Ekaterina N. Berezhnaya ^8,9, Ivan A.Yakovlev ¹⁰, Artur A. Isaev ¹⁰, Roman V. Deev ^{9, 10}
DOI 10.36185/2532-1900-059

How to define and enhance diagnostic and assistance pathways in neuromuscular diseases during the COVID-19 pandemic: the concept of network

Guja Astrea ¹, Gemma Marinella ^1,2, Caterina Agosto ³, Delia Gagliardi ⁴, Marina Grandis ⁵, Maria Giuliano ⁶, Luisa Politano ⁷
DOI 10.36185/2532-1900-060

BAG3-related myofibrillar myopathy: a further observation with cardiomyopathy at onset in pediatric age

Gaia Scarpini ¹, Maria Lucia Valentino ^2,3, Melania Giannotta ¹, Luca Ragni ⁴, Annalaura Torella ⁵, Marta Columbaro ⁶, Vincenzo Nigro ⁵, Antonella Pini ¹
DOI 10.36185/2532-1900-061

Early treatment with Ataluren of a 2-year-old boy with nonsense mutation Duchenne dystrophy

Ilaria Bitetti ¹, Cinzia Mautone ¹, Marianna Bertella ², Maria Rosaria Manna ², Antonio Varone ¹
DOI 10.36185/2532-1900-062

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