John Vissing
Clinical Professor
- Published
MRI in Neuromuscular Diseases: An Emerging Diagnostic Tool and Biomarker for Prognosis and Efficacy
Dahlqvist, J. R., Widholm, P., Leinhard, O. D. & Vissing, John, 2020, In: Annals of Neurology. 88, 4, p. 669-681Research output: Contribution to journal › Review › Research › peer-review
- Published
A quantitative method to assess muscle edema using short TI inversion recovery MRI
Dahlqvist, J. R., Salim, R., Thomsen, C. & Vissing, John, 1 Dec 2020, In: Scientific Reports. 10, 1, 7 p., 7246 .Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Exercise Therapy in Spinobulbar Muscular Atrophy and Other Neuromuscular Disorders
Dahlqvist, J. R. & Vissing, John, Mar 2016, In: Journal of Molecular Neuroscience. 58, 3, p. 388-93 6 p.Research output: Contribution to journal › Journal article › 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
264th ENMC International Workshop: Multi-system involvement in spinal muscular atrophy Hoofddorp, the Netherlands, November 19th – 21st 2021
Industry participants, I. P. & Workshop Participants, W. P., 2022, In: Neuromuscular Disorders. 32, 8, p. 697-705 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Long-term Safety and Efficacy of Avalglucosidase Alfa in Patients With Late-Onset Pompe Disease
Dimachkie, M. M., Barohn, R. J., Byrne, B., Goker-Alpan, O., Kishnani, P. S., Ladha, S., Laforêt, P., Mengel, K. E., Peña, L. D. M., Sacconi, S., Straub, V., Trivedi, J., Van Damme, P., Van Der Ploeg, A. T., Vissing, J., Young, P., Haack, K. A., Foster, M., Gilbert, J. M., Miossec, P. & 3 others, , 2022, In: Neurology. 99, 5, p. E536-E548Research output: Contribution to journal › Journal article › Research › peer-review
- Published
MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement
Care4Rare Canada Consortium, C. C. C., Dec 2019, In: Acta Neuropathologica. 138, 6, p. 1013-1031 19 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
High-resolution melting facilitates mutation screening of PYGM in patients with McArdle disease
Duno, M., Quinlivan, R., Vissing, John & Schwartz, M., 2009, In: Annals of Human Genetics. 73, Pt 3, p. 292-297 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
cDNA analyses of CAPN3 enhance mutation detection and reveal a low prevalence of LGMD2A patients in Denmark
Duno, M., Sveen, M. L., Schwartz, M. & Vissing, John, 2008, In: European Journal of Human Genetics. 16, 8, p. 935-940 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Difference in allelic expression of the CLCN1 gene and the possible influence on the myotonia congenita phenotype.
Dunø, M., Colding-Jørgensen, E., Grunnet, Morten, Jespersen, Thomas, Vissing, John & Schwartz, M., 2004, In: European Journal of Human Genetics. 12, 9, p. 738-43 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 915367
Most downloads
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245
downloads
Skeletal muscle metabolism during prolonged exercise in Pompe disease
Research output: Contribution to journal › Journal article › Research › peer-review
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225
downloads
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
downloads
Aerobic Training in Patients with Congenital Myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
Published