John Vissing
Clinical Professor
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Zilucoplan: An Investigational Complement C5 Inhibitor for the Treatment of Acetylcholine Receptor Autoantibody–Positive Generalized Myasthenia Gravis
Howard, J. F., Vissing, John, Gilhus, N. E., Leite, M. I., Utsugisawa, K., Duda, P. W., Farzaneh-Far, R., Murai, H. & Wiendl, H., 2021, In: Expert Opinion on Investigational Drugs. 30, 5, p. 483-493Research output: Contribution to journal › Journal article › Research › peer-review
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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
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β-Galactosidase deficiency in the GLB1 spectrum of lysosomal storage disease can present with severe muscle weakness and atrophy
Pedersen, J. J., Duno, M., Wibrand, F., Hammer, C., Krag, T. & Vissing, John, 2022, In: JIMD Reports. 63, 6, p. 540-545 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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‘Minimal symptom expression’ in patients with acetylcholine receptor antibody-positive refractory generalized myasthenia gravis treated with eculizumab
Vissing, J., Jacob, S., Fujita, K. P., O’Brien, F., Howard, J. F., The REGAIN Study Group, Mazia, C. G., Wilken, M., Barroso, F., Saba, J., Rugiero, M., Bettini, M., Chaves, M., Vidal, G., Garcia, A. D., De Bleecker, J., Van den Abeele, G., de Koning, K., De Mey, K., Mercelis, R. & 36 others, , 2020, In: Journal of Neurology. 267, p. 1991-2001Research 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
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