John Vissing
Clinical Professor
- 2015
- Published
A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans
Krag, T. O. & Vissing, John, Dec 2015, In: Journal of Neuropathology and Experimental Neurology. 74, 12, p. 1137-46 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1
Tasca, G., D'Amico, A., Monforte, M., Nadaj-Pakleza, A., Vialle, M., Fattori, F., Vissing, John, Ricci, E. & Bertini, E., Nov 2015, In: Neuromuscular Disorders. 25, 11, p. 898-903 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A third case of congenital myasthenic syndrome caused by mutations in SCN4A
Witting, N., Werlauff, U., Ballegaard, Martin & Vissing, John, Oct 2015, p. S209-S209. 1 p.Research output: Contribution to conference › Poster › Research › peer-review
- Published
LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies
Løkken, N., Born, A. P., Duno, M. & Vissing, John, Oct 2015, In: Muscle & Nerve. 52, 4, p. 547-53 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Aerobic training and postexercise protein in facioscapulohumeral muscular dystrophy: RCT study
Andersen, G., Prahm, K. P., Dahlqvist, J. R., Citirak, G. & Vissing, John, Aug 2015, In: Neurology. 85, 5, p. 396-403 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Lactate and Energy Metabolism During Exercise in Patients With Blocked Glycogenolysis (McArdle Disease)
Ørngreen, M. C., Jeppesen, T. D., Taivassalo, T., Hauerslev, S., Preisler, N., Heinicke, K., Haller, R. G., Vissing, John & van Hall, Gerrit, Aug 2015, In: Journal of Clinical Endocrinology and Metabolism. 100, 8, p. E1096-E1104 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Training improves oxidative capacity, but not function, in spinal muscular atrophy type III
Madsen, K. L., Wils, Regitze Sølling, Preisler, N., Thøgersen, F., Berthelsen, M. P. & Vissing, John, Aug 2015, In: Muscle & Nerve. 52, 2, p. 240–244 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Differences in genetic defects and morphology of eye- and limb muscles in mitochondrial myopathy
Levison, L., Dunø, M., Risom, L., Toft, Peter Bjerre & Vissing, John, Jun 2015, In: Acta Ophthalmologica. 93, 4, p. e306-8Research output: Contribution to journal › Comment/debate › Research › peer-review
- Published
Exercise in muscle glycogen storage diseases
Preisler, N. R., Haller, R. G. & Vissing, John, May 2015, In: Journal of Inherited Metabolic Disease. 38, 3, p. 551-63 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E
Semplicini, C., Vissing, John, Dahlqvist, J. R., Stojkovic, T., Bello, L., Witting, N., Duno, M., Leturcq, F., Bertolin, C., D'Ambrosio, P., Eymard, B., Angelini, C., Politano, L., Laforêt, P. & Pegoraro, E., 28 Apr 2015, In: Neurology. 84, 17, p. 1772-81 10 p.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
Published -
225
downloads
Reliability of the 2- and 6-minute walk tests in neuromuscular diseases
Research output: Contribution to journal › Letter › Research › peer-review
Published -
185
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Aerobic Training in Patients with Congenital Myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
Published