John Vissing
Clinical Professor
- 2022
- Published
Home-based gait analysis as an exploratory endpoint during a multicenter phase 1 trial in limb girdle muscular dystrophy type R2 and facioscapulohumeral muscular dystrophy
Gidaro, T., Gasnier, E., Annoussamy, M., Vissing, John, Attarian, S., Mozaffar, T., Iyadurai, S., Wagner, K. R., Vissiere, D., Walker, G., Shukla, S. S. & Servais, L., 2022, In: Muscle & Nerve. 65, 2, p. 237-242 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Muscle MRI in McArdle Disease: A European Multicenter Observational Study
Løkken, N., Revsbech, K. L., Jacobsen, L. N., Martinuzzi, A., Martin, M. Á., Díaz-Manera, J., Dominguez-Gonzalez, C., Brondani, G., Musumeci, O., Granata, F., Stefan, C., Merino-Sanchez, C., Peralta, C. N., Khawajazada, T., Alonso-Pérez, J., Toscano, A. & Vissing, John, 2022, In: Neurology. 99, 15, p. E1664-E1675Research output: Contribution to journal › Journal article › Research › peer-review
- Published
No effect of oral ketone ester supplementation on exercise capacity in patients with McArdle disease and healthy controls: A randomized placebo-controlled cross-over study
Løkken, N., Storgaard, J. H., Revsbech, K. L., Voermans, N. C., van Hall, Gerrit, Vissing, John & Ørngreen, M. C., 2022, In: Journal of Inherited Metabolic Disease. 45, 3, p. 502-516 15 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Global FKRP registry - the research database for limb girdle muscular dystrophy R9 (2I)
Murphy, L., Alfano, L., Brazzo, K., Johnson, N., Laurent, J., Mathews, K., Thiele, S., Vissing, John, Walter, M., Woods, L., Orstavik, K. & Straub, V., Oct 2022, In: Neuromuscular Disorders. 32, Supplement 1, p. S118-S118 1 p., P.175.Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
- Published
Growth Factors Do Not Improve Muscle Function in Young or Adult mdx Mice
Nielsen, T. L., Hornsyld, T. M., Pinós, T., Brolin, C., Vissing, John & Krag, T. O., 2022, In: Biomedicines. 10, 2, 304.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
β-Galactosidase deficiency in the GLB1 spectrum of lysosomal storage disease can present with severe muscle weakness and atrophy
Pedersen, J. J., Duno, M., Wibrand, F., Hammer, C., Krag, T. & Vissing, John, 2022, In: JIMD Reports. 63, 6, p. 540-545 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohort
Quijano-Roy, S., Haberlova, J., Castiglioni, C., Vissing, J., Munell, F., Rivier, F., Stojkovic, T., Malfatti, E., Gómez García de la Banda, M., Tasca, G., Costa Comellas, L., Benezit, A., Amthor, H., Dabaj, I., Gontijo Camelo, C., Laforêt, P., Rendu, J., Romero, N. B., Cavassa, E., Fattori, F. & 10 others, , 2022, In: Journal of Neurology. 269, p. 2414–2429Research output: Contribution to journal › Journal article › Research › peer-review
- Published
No effect of triheptanoin in patients with phosphofructokinase deficiency
Raaschou-Pedersen, D. E., Madsen, K. L., Lokken, N., Storgaard, J. H., Quinlivan, R., Laforet, P., Lund, Allan Meldgaard, van Hall, Gerrit, Vissing, John & Orngreen, M., Apr 2022, In: Neuromuscular Disorders. 32, 4, p. 295-304 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy
Ranu, N., Laitila, J., Dugdale, H. F., Mariano, J., Kolb, J. S., Wallgren-Pettersson, C., Witting, N., Vissing, J., Vilchez, J. J., Fiorillo, C., Zanoteli, E., Auranen, M., Jokela, M., Tasca, G., Claeys, K. G., Voermans, N. C., Palmio, J., Huovinen, S., Moggio, M., Beck, T. N. & 3 others, , 2022, In: Acta Neuropathologica Communications. 10, 185.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
High Resolution Analysis of DMPK Hypermethylation and Repeat Interruptions in Myotonic Dystrophy Type 1
Rasmussen, A., Hildonen, M., Vissing, John, Duno, M., Tümer, Asuman Zeynep & Birkedal, U., 2022, In: Genes. 13, 6, 12 p., 970.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 915367
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245
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Skeletal muscle metabolism during prolonged exercise in Pompe disease
Research output: Contribution to journal › Journal article › Research › peer-review
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225
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Reliability of the 2- and 6-minute walk tests in neuromuscular diseases
Research output: Contribution to journal › Letter › Research › peer-review
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185
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Aerobic Training in Patients with Congenital Myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
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