Exercise training in metabolic myopathies von Vissing, J.

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Exercise treatment in muscle disorders von Vissing, J

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Episodic hyperCKaemia may be a feature of α‐methylacyl‐coenzyme A racemase deficiency von Krett, B., Straub, V., Vissing, J.

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McArdle disease: a clinical review von Quinlivan, R, Buckley, J, James, M, Twist, A, Ball, S, Duno, M, Vissing, J, Bruno, C, Cassandrini, D, Roberts, M, Winer, J, Rose, M, Sewry, C

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Botulinum toxin treatment improves dysphagia in patients with oculopharyngeal muscular dystrophy and sporadic inclusion body myositis von Witting, N., Daugaard, D., Prytz, S., Biernat, H., Diederichsen, L. P., Vissing, J.

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Development of Continuum of Care for McArdle disease: A practical tool for clinicians and patients von Reason, S.L., Voermans, N., Lucia, A., Vissing, J., Quinlivan, R., Bhai, S., Wakelin, A.

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European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10‐year experience von Ploeg, A. T., Kruijshaar, M. E., Toscano, A., Laforêt, P., Angelini, C., Lachmann, R. H., Pascual Pascual, S. I., Roberts, M., Rösler, K., Stulnig, T., Doorn, P. A., Van den Bergh, P. Y. K., Vissing, J., Schoser, B., Bembi, Bruno, Broomfield, Alexander, Boentert, Matthias, Desnuelle, Claude, Findling, Oliver, Hahn, Andreas, Díaz‐Manera, Jordi, Hundsberger, Thomas, Kornblum, Cornelia, Labarthé, Franҫois, Laforet, Pascal, Mengel, Karl‐Eugen, Mongini, Tiziana, Muller‐Felber, Wolfgang, Parenti, Giancarlo, Pijnappel, W. Pim, Preisler, Nicolai, Sacconi, Sabrina, Talim, Beril, Tardieu, Marine, Beek, Nadine A.M.E, Wenninger, Stephan

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MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement von Donkervoort, S., Sabouny, R., Yun, P., Gauquelin, L., Chao, K. R., Hu, Y., Al Khatib, I., Töpf, A., Mohassel, P., Cummings, B. B., Kaur, R., Saade, D., Moore, S. A., Waddell, L. B., Farrar, M. A., Goodrich, J. K., Uapinyoying, P., Chan, S.H. S., Javed, A., Leach, M. E., Karachunski, P., Dalton, J., Medne, L., Harper, A., Thompson, C., Thiffault, I., Specht, S., Lamont, R. E., Saunders, C., Racher, H., Bernier, F. P., Mowat, D., Witting, N., Vissing, J., Hanson, R., Coffman, K. A., Hainlen, M., Parboosingh, J. S., Carnevale, A., Yoon, G., Schnur, R. E., Boycott, K. M., Mah, J. K., Straub, V., Foley, A. Reghan, Innes, A. M., Bönnemann, C. G., Shutt, T. E.

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667P Glycogen response to enzyme replacement therapy in patients with Pompe disease von Stemmerik, M., Vissing, J.

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Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment? von Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P.L., Fiuza-Luces, C., Andreu, A.L., Rodríguez-Aguilera, J.C., Martín, M.A., Arenas, J., Vissing, J., Lucia, A., Krag, T.O., Pinós, T.

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Mitochondrial dysfunction and risk of cancer von Lund, M, Melbye, M, Diaz, L J, Duno, M, Wohlfahrt, J, Vissing, J

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Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging von Giacomucci, G., Monforte, M., Diaz‐Manera, J., Mul, K., Fernandez Torrón, R., Maggi, L., Marini Bettolo, C., Dahlqvist, J. R., Haberlova, J., Camaño, P., Gros, M., Tartaglione, T., Cristiano, L., Gerevini, S., Calandra, P., Deidda, G., Giardina, E., Sacconi, S., Straub, V., Vissing, J., Van Engelen, B., Ricci, E., Tasca, G.

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Fatigue in patients with spinal muscular atrophy type II and congenital myopathies: evaluation of the fatigue severity scale von Werlauff, Ulla, Højberg, A., Firla-Holme, R., Steffensen, B. F., Vissing, J.

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Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N‐related myopathies von Bachmann, Christoph, Noreen, Faiza, Voermans, Nicol C., Schär, Primo L., Vissing, John, Fock, Johanna M., Bulk, Saskia, Kusters, Benno, Moore, Steven A., Beggs, Alan H., Mathews, Katherine D., Meyer, Megan, Genetti, Casie A., Meola, Giovanni, Cardani, Rosanna, Mathews, Emma, Jungbluth, Heinz, Muntoni, Francesco, Zorzato, Francesco, Treves, Susan

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A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy von Riisager, M, Duno, M, Hansen, F. Juul, Krag, T.O, Vissing, C.R, Vissing, J

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Paraspinal fat infiltration in healthy adults with aging von Dahlqvist, J, Vissing, C, Hedermann, G, Thomsen, C, Vissing, J

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Endocrine function over time in patients with myotonic dystrophy type 1 von Dahlqvist, J. R., Ørngreen, M. C., Witting, N., Vissing, J.

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Carbohydrate- and protein-rich diets in McArdle disease: effects on exercise capacity von Andersen, S T, Vissing, J

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Prevalence of migraine in persons with the 3243A>G mutation in mitochondrial DNA von Guo, S., Esserlind, A.-L., Andersson, Z., Frederiksen, A. L., Olesen, J., Vissing, J., Ashina, M.

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M.I.2 Metabolic assessments of muscle disease von Vissing, J

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