John Vissing
Clinical Professor
- 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
A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood
Born, A. P., Duno, M., Rafiq, J., Risom, L., Wibrand, F., Østergaard, Elsebet & Vissing, John, Jan 2015, In: European Journal of Paediatric Neurology. 19, 1, p. 69-71 3 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
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
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
- Published
Clinical and neurophysiological response to pharmacological treatment of DOK7 congenital myasthenia in an older patient
Witting, N., Crone, C., Duno, M. & Vissing, John, Mar 2015, In: Clinical Neurology and Neurosurgery. 130, p. 168-70 3 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
Endocrine function over time in patients with myotonic dystrophy type 1
Dahlqvist, J. R., Ørngreen, M. C., Witting, N. & Vissing, John, Jan 2015, In: European Journal of Neurology. 22, 1, p. 116-122 7 p.Research output: Contribution to journal › Journal article › 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
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
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
Published