Guidance for the management of myasthenia gravis (MG) and Lambert-Eaton myasthenic syndrome (LEMS) during the COVID-19 pandemic von Jacob, Saiju, Muppidi, Srikanth, Guidon, Amanda, Guptill, Jeffrey, Hehir, Michael, Howard, James F., Illa, Isabel, Mantegazza, Renato, Murai, Hiroyuki, Utsugisawa, Kimiaki, Vissing, John, Wiendl, Heinz, Nowak, Richard J.

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229th ENMC international workshop: Limb girdle muscular dystrophies – Nomenclature and reformed classification Naarden, the Netherlands, 17–19 March 2017 von Straub, Volker, Murphy, Alexander, Udd, Bjarne, Corrado, Angelini, Aymé, Ségolène, Bönneman, Carsten, de Visser, Marianne, Hamosh, Ada, Jacobs, Laura, Khizanishvili, Nina, Kroneman, Madelon, Laflorêt, Pascal, Murphy, Alex, Nigro, Vincenzo, Rufibach, Laura, Sarkozy, Anna, Swanepoel, Shaun, Torrente, Ivan, Udd, Bjarne, Urtizberea, Andoni, Vissing, John, Walter, Maggie

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Therapeutic advances in neuromuscular diseases in 2023 von Vissing, John

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Pharmacologic Treatment of Downstream of Tyrosine Kinase 7 Congenital Myasthenic Syndrome von Witting, Nanna, Vissing, John

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Aerobic Training in Patients with Congenital Myopathy von Hedermann, Gitte, Vissing, Christoffer Rasmus, Heje, Karen, Preisler, Nicolai, Witting, Nanna, Vissing, John

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Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies von Vissing, John

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Accuracy of a machine learning muscle MRI-based tool for the diagnosis of muscular dystrophies von Verdú-Díaz, José, Alonso-Pérez, Jorge, Nuñez-Peralta, Claudia, Tasca, Giorgio, Vissing, John, Straub, Volker, Fernández-Torrón, Roberto, Llauger, Jaume, Illa, Isabel, Díaz-Manera, Jordi

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Paternal comeback in mitochondrial DNA inheritance von Vissing, John

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Muscle fat replacement and contractility in patients with skeletal muscle sodium channel disorders von Pedersen, Jonas Jalili, Stemmerik, Mads Godtfeldt, Jacobsen, Laura Nørager, Skriver, Sofie Vinther, Wilms, Gustav Rhode, Duno, Morten, Vissing, John

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Physical activity in myotonic dystrophy type 1 von Knak, Kirsten Lykke, Sheikh, Aisha Munawar, Witting, Nanna, Vissing, John

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Quantitative muscle MRI as an assessment tool for monitoring disease progression in LGMD2I: a multicentre longitudinal study von Willis, Tracey A, Hollingsworth, Kieren G, Coombs, Anna, Sveen, Marie-Louise, Andersen, Søren, Stojkovic, Tanya, Eagle, Michelle, Mayhew, Anna, de Sousa, Paulo L, Dewar, Liz, Morrow, Jasper M, Sinclair, Christopher D J, Thornton, John S, Bushby, Kate, Lochmüller, Hanns, Hanna, Michael G, Hogrel, Jean-Yves, Carlier, Pierre G, Vissing, John, Straub, Volker

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Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation von Karazi, Walaa, Scalco, Renata S, Stemmerik, Mads G, Løkken, Nicoline, Lucia, Alejandro, Santalla, Alfredo, Martinuzzi, Andrea, Vavla, Marinela, Reni, Gianluigi, Toscano, Antonio, Musumeci, Olimpia, Kouwenberg, Carlyn V, Laforêt, Pascal, Millán, Beatriz San, Vieitez, Irene, Siciliano, Gabriele, Kühnle, Enrico, Trost, Rebecca, Sacconi, Sabrina, Durmus, Hacer, Kierdaszuk, Biruta, Wakelin, Andrew, Andreu, Antoni L, Pinós, Tomàs, Marti, Ramon, Quinlivan, Ros, Vissing, John, Voermans, Nicol C

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Decreased variability of the 6-minute walk test by heart rate correction in patients with neuromuscular disease von Prahm, Kira P, Witting, Nanna, Vissing, John

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High Resolution Analysis of DMPK Hypermethylation and Repeat Interruptions in Myotonic Dystrophy Type 1 von Rasmussen, Astrid, Hildonen, Mathis, Vissing, John, Duno, Morten, Tümer, Zeynep, Birkedal, Ulf

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Mutation Load of Single, Large-Scale Deletions of mtDNA in Mitotic and Postmitotic Tissues von Jeppesen, Tina D., Duno, Morten, Vissing, John

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Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency von Preisler, Nicolai, Cohen, Jonathan, Vissing, Christoffer Rasmus, Madsen, Karen Lindhardt, Heinicke, Katja, Sharp, Lydia Jane, Phillips, Lauren, Romain, Nadine, Park, Sun Young, Newby, Marta, Wyrick, Phil, Mancias, Pedro, Galbo, Henrik, Vissing, John, Haller, Ronald Gerald

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Antimyostatin Treatment in Health and Disease: The Story of Great Expectations and Limited Success von Nielsen, Tue L., Vissing, John, Krag, Thomas O.

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Muscle atrophy reversed by growth factor activation of satellite cells in a mouse muscle atrophy model von Hauerslev, Simon, Vissing, John, Krag, Thomas O

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High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 2I in Denmark von Sveen, Marie-Louise, Schwartz, Marianne, Vissing, John

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Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E von Semplicini, Claudio, Vissing, John, Dahlqvist, Julia R, Stojkovic, Tanya, Bello, Luca, Witting, Nanna, Duno, Morten, Leturcq, France, Bertolin, Cinzia, DʼAmbrosio, Paola, Eymard, Bruno, Angelini, Corrado, Politano, Luisa, Laforêt, Pascal, Pegoraro, Elena

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