John Vissing
Clinical Professor
- Published
Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy
Böhm, J., Biancalana, V., Dechene, E. T., Bitoun, M., Pierson, C. R., Schaefer, E., Karasoy, H., Dempsey, M. A., Klein, F., Dondaine, N., Kretz, C., Haumesser, N., Poirson, C., Toussaint, A., Greenleaf, R. S., Barger, M. A., Mahoney, L. J., Kang, P. B., Zanoteli, E., Vissing, J. & 48 others, , 2012, In: Human Mutation. 33, 6, p. 949-59 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Calpain 3 is important for muscle regeneration: evidence from patients with limb girdle muscular dystrophies
Hauerslev, S., Sveen, M., Duno, M., Angelini, C., Vissing, John & Krag, T. O., 2012, In: B M C Musculoskeletal Disorders. 13, p. 43-53 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Neuromuskulære sygdomme
Jakobsen, J. K. & Vissing, John, 2012, Medicin. Lærebog i medicin. Baslund, B., Feldt-Rasmussen, U., Kastrup, J. & Sørensen, P. S. (eds.). p. 1099 18 p.Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review
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Influence of erythrocyte oxygenation and intravascular ATP on resting and exercising skeletal muscle blood flow in humans with mitochondrial myopathy
Jeppesen, T. D., Vissing, John & González-Alonso, J., 2012, In: Mitochondrion. 44, 5, p. 703-709Research output: Contribution to journal › Journal article › Research › peer-review
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Blocked muscle fat oxidation during exercise in neutral lipid storage disease
Laforêt, P., Ørngreen, M., Preisler, N., Andersen, G. & Vissing, John, 2012, In: Archives of Neurology. 69, 4, p. 530-3 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Cardiac manifestations of myotonic dystrophy type 1
Petri, H., Vissing, John, Witting, N., Bundgaard, H. & Køber, Lars Valeur, 2012, In: International Journal of Cardiology. 160, 2, p. 82-8 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Muscle phosphorylase kinase deficiency: a neutral metabolic variant or a disease?
Preisler, N., Orngreen, M. C., Echaniz-Laguna, A., Laforet, P., Lonsdorfer-Wolf, E., Doutreleau, S., Geny, B., Akman, H. O., Dimauro, S. & Vissing, John, 2012, In: Neurology. 78, 4, p. 265-8 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Fat and carbohydrate metabolism during exercise in late-onset Pompe disease
Preisler, N., Laforet, P., Madsen, K. L., Wils, Regitze Sølling, Lukacs, Z., Ørngreen, M. C., Lacour, A. & Vissing, John, 2012, In: Molecular Genetics and Metabolism. 107, 3, p. 462-8 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Mechanisms of exertional fatigue in muscle glycogenoses
Vissing, John & Haller, R. G., 2012, In: Neuromuscular Disorders. 22 Suppl 3, p. S168-71Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Change in muscle strength over time in spinal muscular atrophy types II and III. A long-term follow-up study
Werlauff, U., Vissing, John & Steffensen, B. F., 2012, In: Neuromuscular Disorders. 22, 12, p. 1069-74 6 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