John Vissing
Clinical Professor
- 2017
- Published
211th ENMC International Workshop: Development of diagnostic criteria and management strategies for McArdle Disease and related rare glycogenolytic disorders to improve standards of care. 17-19 April 2015, Naarden, The Netherlands
Workshop Participants, W. P. & Vissing, John, 2017, In: Neuromuscular Disorders. 27, 12, p. 1143-1151Research output: Contribution to journal › Comment/debate › Research
- Published
Aerobic anti-gravity exercise in patients with Charcot-Marie-Tooth disease types 1A and X: A pilot study
Knak, K. L., Andersen, L. K. & Vissing, John, 2017, In: Brain and Behavior. 7, 12, 5 p., e00794.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Aerobic training in myotonia congenita: Effect on myotonia and fitness
Andersen, G., Løkken, N. & Vissing, John, 2017, In: Muscle and Nerve. 56, 4, p. 696-699 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Fat Replacement of Paraspinal Muscles with Aging in Healthy Adults
Dahlqvist, J. R., Vissing, C. R., Hedermann, G., Thomsen, C. & Vissing, John, 2017, In: Medicine and Science in Sports and Exercise. 49, 3, p. 595-601Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Glycogen synthesis in glycogenin 1-deficient patients: A role for glycogenin 2 in muscle
Krag, T. O., Ruiz-Ruiz, C. & Vissing, John, 2017, In: Journal of Clinical Endocrinology and Metabolism. 102, 8, p. 2690-2700 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial
Andersen, G., Heje, K., Buch, A. E. & Vissing, John, 2017, In: Journal of Neurology. 264, 6, p. 1099-1106Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Human growth hormone stabilizes walking and improves strength in a patient with dominantly inherited calpainopathy
Prahm, K. P., Feldt-Rasmussen, Ulla & Vissing, John, 2017, In: Neuromuscular Disorders. 27, 4, p. 358-362Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiency
Preisler, N., Cohen, J., Vissing, C. R., Madsen, K. L., Heinicke, K., Sharp, L. J., Phillips, L., Romain, N., Park, S. Y., Newby, M., Wyrick, P., Mancias, P., Galbo, Henrik, Vissing, John & Haller, R. G., 2017, In: Molecular Genetics and Metabolism. 122, 3, p. 117-121Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Leber hereditary optic neuropathy due to a new ND1 mutation
Soldath, P., Wegener, Marianne, Sander, B., Rosenberg, T., Duno, M., Wibrand, F. & Vissing, John, 2017, In: Ophthalmic Genetics. 38, 5, p. 480-485 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients
Andersen, G., Dahlqvist, J. R., Vissing, C. R., Heje, K., Thomsen, C. & Vissing, John, 2017, In: Journal of Neurology. 264, 3, p. 438-447Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mitochondrial Point Mutation m.3243A>G Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study
Langdahl, J. H., Frederiksen, A. L., Hansen, S. J., Andersen, P. H., Yderstraede, K. B., Dunø, M., Vissing, John & Frost, M., 2017, In: Journal of Bone and Mineral Research. 32, 10, p. 2041-2048Research output: Contribution to journal › Journal article › Research › peer-review
- Published
PGM1 deficiency: Substrate use during exercise and effect of treatment with galactose
Voermans, N. C., Preisler, N., Madsen, K. L., Janssen, M. C. H., Kusters, B., Abu Bakar, N., Conte, F., Lamberti, V. M. L., Nusman, F., van Engelen, B. G., van Scherpenzeel, M., Vissing, John & Lefeber, D. J., 2017, In: Neuromuscular Disorders. 27, 4, p. 370-376Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Reliability of the 2- and 6-minute walk tests in neuromuscular diseases
Knak, K. L., Andersen, L. K., Witting, N. & Vissing, John, 2017, In: Journal of Rehabilitation Medicine. 49, 4, p. 362-366 5 p.Research output: Contribution to journal › Letter › Research › peer-review
- Published
Reply: Dominant LGMD2A: Alternative diagnosis or hidden digenism?
Vissing, John & Duno, M., 2017, In: Brain. 140, 2, 2 p., e8.Research output: Contribution to journal › Comment/debate › Research
- Published
The antimyotonic effect of lamotrigine in non-dystrophic myotonias: a double-blind randomized study
Andersen, G., Hedermann, G., Witting, N., Duno, M., Andersen, H. & Vissing, John, 2017, In: Brain. 140, 9, p. 2295-2305Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Treatment Opportunities in Patients With Metabolic Myopathies
Ørngreen, M. C. & Vissing, John, 2017, In: Current Treatment Options in Neurology. 19, 11, 16 p., 37.Research output: Contribution to journal › Review › Research › peer-review
- Published
Update on new muscle glycogenosis
Laforêt, P., Malfatti, E. & Vissing, John, 2017, In: Current Opinion in Neurology. 30, 5, p. 449-456Research output: Contribution to journal › Review › Research › peer-review
- Published
Dysphagia is prevalent in patients with CPEO and single, large-scale deletions in mtDNA
Pedersen, G. H., Løkken, N., Dahlqvist, J. R. & Vissing, John, Jan 2017, In: Mitochondrion. 32, p. 27-30 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Effects of Sildenafil on Cerebrovascular Reactivity in Patients with Becker Muscular Dystrophy
Lindberg, U., Witting, N., Jørgensen, S. L., Vissing, John, Rostrup, E., Larsson, Henrik Bo Wiberg & Kruuse, Christina Rostrup, Jan 2017, In: Neurotherapeutics. 14, 1, p. 182-190Research output: Contribution to journal › Journal article › Research › peer-review
- Published
SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy
Svenstrup, K., Nielsen, T. T., Aidt, F., Rostgaard, N., Duno, M., Wibrand, F., Vinther-Jensen, T., Law, Ian, Vissing, John, Roos, P., Hjermind, L. E. & Nielsen, Jørgen Erik, Feb 2017, In: The Cerebellum. 16, 1, p. 62-67 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Phenotypes, genotypes, and prevalence of congenital myopathies older than 5 years in Denmark
Witting, N., Werlauff, U., Duno, M. & Vissing, John, Apr 2017, In: Neurology: Genetics. 3, 2, 15 p., e140.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10-year experience
van der 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. M., van Doorn, P. A., Van den Bergh, P. Y. K., Vissing, John, Schoser, B. & European Pompe Consortium, E. P. C., Jun 2017, In: European Journal of Neurology. 24, 6, p. 768-e31Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Skeletal muscle metabolism during prolonged exercise in Pompe disease
Preisler, N., Laforêt, P., Madsen, K. L., Husu, E., Vissing, C. R., Hedermann, G., Galbo, Henrik, Lindberg, C. & Vissing, John, Aug 2017, In: Endocrine Connections. 6, 6, p. 384-394 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
DOK7 congenital myasthenia may be associated with severe mitral valve insufficiency
Gaist, D., Mogensen, J., Pedersen, E. G., Schrøder, H. D., Vissing, John, Andersen, H. & Hertz, J. M., 15 Aug 2017, In: Journal of the Neurological Sciences. 379, p. 217-218 2 p.Research output: Contribution to journal › Comment/debate › Research
- Published
Pure exercise intolerance and ophthalmoplegia associated with the m.12,294G > A mutation in the MT-TL2 gene: a case report
Soldath, P., Madsen, K. L., Buch, A. E., Duno, M., Wibrand, F. & Vissing, John, Oct 2017, In: BMC Musculoskeletal Disorders. 18, 6 p., 419.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 915367
Most downloads
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246
downloads
Skeletal muscle metabolism during prolonged exercise in Pompe disease
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
226
downloads
Reliability of the 2- and 6-minute walk tests in neuromuscular diseases
Research output: Contribution to journal › Letter › Research › peer-review
Published -
186
downloads
Aerobic Training in Patients with Congenital Myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
Published