New graphic for Acta Myologica
Luisa Politano
Fascicolo 1-2020
Editorial
Original article
Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online survey
David C. Schorling 1, Cornelia K. Müller 1, Astrid Pechmann 1, Sabine Borell 1, Thorsten Langer 1, Simone Thiele 2, Maggie C. Walter 2, Barbara Zieger 3, Janbernd Kirschner 1,4
DOI 10.36185/2532-1900-001
Identification, molecular characterization and segregation analysis of a variant DMPK pre-mutation allele in a three-generation Italian family
Luana Fontana 1, Massimo Santoro 2, Maria Rosaria D’Apice 3, Francesca Peluso 4, Giulia Gori 3, Amelia Morrone 5, Giuseppe Novelli 1,3,6, Laura Dosa 7, Annalisa Botta 1
DOI 10.36185/2532-1900-002
Late-onset MADD: a rare cause of cirrhosis and acute liver failure?
Patrick Soldath 1,2, Allan Lund 1,3, John Vissing 1,2
DOI 10.36185/2532-1900-003
Laing early-onset distal myopathy with subsarcolemmal hyaline bodies caused by a novel variant in the MYH7 gene
Luís Negrão 1, Rita Machado 1, Miguel Lourenço 2, Ana Fernandez-Marmiesse 3,4, Olinda Rebelo 1
DOI 10.36185/2532-1900-004
Case report
Facioscapulohumeral muscular dystrophy (FSHD) and multiple sclerosis: a case report
Rosa Iodice 1, Lorenzo Ugga 2, Francesco Aruta 1, Aniello Iovino 1, Lucia Ruggiero 1
DOI 10.36185/2532-1900-005
Myotonic dystrophy type 1 and high ventricular vulnerability at the electrophysiological evaluation: ICD yes or not?
Giusy Sirico 1, Andrea Montisci 2, Francesco Secchi 3,4, Massimo Mantica 1
DOI 10.36185/2532-1900-006
Neuromuscular tetanic hyperexcitability syndrome associated to a heterozygous Kv1.1 N255D mutation with normal serum magnesium levels
Francesca Bianchi 1, Costanza Simoncini 1, Raffaella Brugnoni 2, Giulia Ricci 1, Gabriele Siciliano 1
DOI 10.36185/2532-1900-007
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