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Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase

Eleonora Mauri ^1*, Elena Abati ^1,2*, Olimpia Musumeci ³, Carmelo Rodolico ³, Maria Grazia D’Angelo ⁴, Massimiliano Mirabella ⁵, Matteo Lucchini ⁵, Luca Bello ⁶, Elena Pegoraro ⁶, Lorenzo Maggi ⁷, Letizia Manneschi ⁸, Chiara Gemelli ^9,10, Marina Grandis ^10,11, Angela Zuppa ^10,11, Sara Massucco ^10,11, Luana Benedetti ^10,11, Claudia Caponnetto ^10,11, Angelo Schenone ^10,11, Alessandro Prelle ¹², Stefano C. Previtali ¹³, Marina Scarlato ¹³, Adele D’Amico ¹⁴, Enrico Bertini ¹⁴, Elena M. Pennisi ¹⁵, Laura De Giglio ¹⁵, Marika Pane ¹⁶, Eugenio Mercuri ¹⁶, Tiziana Mongini ¹⁷, Federica Ricci ¹⁷, Angela Berardinelli ¹⁸, Guja Astrea ¹⁹, Sara Lenzi ¹⁹, Roberta Battini ^19,20, Giulia Ricci ²⁰, Francesca Torri ²⁰, Gabriele Siciliano ²⁰, Filippo M. Santorelli ²¹, Alessandra Ariatti ²², Massimiliano Filosto ²³, Luigia Passamano ²⁴, Luisa Politano ²⁴, Marianna Scutifero ²⁴, Paola Tonin ²⁵, Barbara Fossati ²⁶, Chiara Panicucci ²⁷, Claudio Bruno ²⁷, Sabrina Ravaglia ²⁸, Mauro Monforte ²⁹, Giorgio Tasca ²⁹, Enzo Ricci ²⁹, Antonio Petrucci ³⁰, Lucio Santoro ³¹, Lucia Ruggiero ³¹, Andrea Barp ³², Emilio Albamonte ³², Valeria Sansone ³², Delia Gagliardi ², Gianluca Costamagna ², Alessandra Govoni ^1,20, Francesca Magri ¹, Roberta Brusa ¹, Daniele Velardo ³⁴, Megi Meneri ¹, Monica Sciacco ³⁴, Stefania Corti ^1,2, Nereo Bresolin ^1,2, Isabella Moroni ³⁴, Sonia Messina ³, Antonio Di Muzio ³⁵, Vincenzo Nigro ³⁶, Rocco Liguori ³⁷, Giovanni Antonini ³⁸, Antonio Toscano ³, Carlo Minetti ³⁹, Giacomo Pietro Comi ^2,33, Italian Association of Myology
DOI 10.36185/2532-1900-008

Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis

Francesca Magri ¹, Roberta Brusa ¹, Luca Bello ³, Lorenzo Peverelli ⁴, Roberto Del Bo ¹, Alessandra Govoni ¹, Claudia Cinnante ⁵, Irene Colombo ⁴, Francesco Fortunato ¹, Roberto Tironi ⁴, Stefania Corti ^1,2, Nadia Grimoldi ⁶, Monica Sciacco ⁴, Nereo Bresolin ¹, Elena Pegoraro ³, Maurizio Moggio ⁴, Giacomo Pietro Comi ^2,4
DOI 10.36185/2532-1900-009

Maximum bite force in patients with spinal muscular atrophy during the first year of nusinersen therapy – A pilot study

Teresa Kruse ^1,2, Raoul Heller ^2,3, Brunhilde Wirth ^2,3,4, Julia Glöggler ⁵, Claudia D. Wurster ⁶, Albert C. Ludolph ⁶, Bert Braumann ^1,2
DOI 10.36185/2532-1900-010

Efficacy and safety of ropivacaine HCl in peribulbar anaesthesia for cataract surgery in patients with myotonic dystrophy type 1

Alberto Palladino ¹, Maddalena De Bernardo ², Marianna Scutifero ¹, Michele Lanza ³, Silvio De Querquis ⁴, Nicola Rosa ², Luisa Politano ¹
DOI 10.36185/2532-1900-011

Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in TK2 gene

George K. Papadimas ¹, Efthimia Vargiami ², Pinelopi Dragoumi ², Rudy Van Coster ³, Joel Smet ³, Sara Seneca ⁴, Constantinos Papadopoulos ¹, Evangelia Kararizou ¹, Dimitrios Zafeiriou ²
DOI 10.36185/2532-1900-012

Respiratory muscle involvement in HNRNPDL LGMD D3 muscular dystrophy: an extensive clinical description of the first Italian patient

Edoardo Malfatti ¹, Denise Cassandrini ², Anna Rubegni ², Filippo M. Sartorelli ², Marcello Villanova ³
DOI 10.36185/2532-1900-013

MPV promote adherence to nocturnal NIV in a Duchenne patient

Anna Annunziata, Antonietta Coppola, Antonella Marotta, Giuseppe Fiorentino
DOI 10.36185/2532-1900-014