John Vissing
Clinical Professor
- Published
Clinical presentation and mutations in Danish patients with Wilson disease
Møller, L. B., Horn, N., Jeppesen, T. D., Vissing, John, Wibrand, F., Jennum, Poul & Ott, P., 2011, In: European Journal of Human Genetics. 19, 9, p. 935-41 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Collagen XII myopathy with rectus femoris atrophy and collagen XII retention in fibroblasts
Witting, N., Krag, T., Werlauff, U., Duno, M., Oestergaard, S. T., Dahlqvist, J. R. & Vissing, John, 2018, In: Muscle & Nerve. 57, 6, p. 1026-1030Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Combined Muscle Biopsy and Comprehensive Electrophysiology in General Anesthesia is Valuable in Diagnosis of Neuromuscular Disease in Children
Høi-Hansen, Christina Engel, Tygesen, M. L. B., Dunø, M., Vissing, John, Ballegaard, Martin & Born, P., 2021, In: Neuropediatrics. 52, 6, p. 462-468Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Congenital Titinopathy: Comprehensive characterization and pathogenic insights
Oates, E. C., Jones, K. J., Donkervoort, S., Charlton, A., Brammah, S., Smith, J. E., Ware, J. S., Yau, K. S., Swanson, L. C., Whiffin, N., Peduto, A. J., Bournazos, A., Waddell, L. B., Farrar, M. A., Sampaio, H. A., Teoh, H. L., Lamont, P. J., Mowat, D., Fitzsimons, R. B., Corbett, A. J. & 64 others, , 2018, In: Annals of Neurology. 83, 6, p. 1105-1124 20 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Congenital myopathies are mainly associated with a mild cardiac phenotype
Petri, H., Wahbi, K., Witting, N., Køber, Lars Valeur, Bundgård, Henning, Kamoun, E., Vellieux, G., Stojkovic, T., Béhin, A., Laforet, P. & Vissing, John, Jun 2019, In: Journal of Neurology. 266, 6, p. 1367-1375 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Contractile properties are disrupted in Becker muscular dystrophy, but not in limb girdle type 2I
Løkken, N., Hedermann, G., Thomsen, C. & Vissing, John, Sep 2016, In: Annals of Neurology. 80, 3, p. 466-471 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Contractile properties are impaired in congenital myopathies
Eisum, A. V., Fornander, F., Poulsen, N. S., Andersen, A. G., Dahlqvist, J., Andersen, L. K., Witting, N. & Vissing, John, 1 Aug 2020, In: Neuromuscular Disorders. 30, 8, p. 649-655 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Correlation between myasthenia gravis-activities of daily living (MG-ADL) and quantitative myasthenia gravis (QMG) assessments of anti-acetylcholine receptor antibody-positive refractory generalized myasthenia gravis in the phase 3 regain study
Vissing, John, O'Brien, F., Wang, J. J. & Howard, J. F., 2018, In: Muscle & Nerve. 58, 2, p. E21-E22Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Creatine kinase response to high-intensity aerobic exercise in adult-onset muscular dystrophy
Andersen, S. P., Sveen, M., Wils, Regitze Sølling, Madsen, K. L., Hansen, J. B., Madsen, M. L. & Vissing, John, 2013, In: Muscle & Nerve. 48, 6, p. 897-901 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)
Pinós, T., Andreu, A. L., Bruno, C., Hadjigeorgiou, G. M., Haller, R., Laforêt, P., Lucía, A., Martín, M. A., Martinuzzi, A., Navarro, C., Oflazer, P., Pouget, J., Quinlivan, R., Sacconi, S., Scalco, R. S., Toscano, A., Vissing, J., Vorgerd, M., Wakelin, A., Martí, R. & 14 others, , 2020, In: Orphanet Journal of Rare Diseases. 15, 1, 187.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cytokine genes as potential biomarkers for muscle weakness in OPMD
Riaz, M., Raz, Y., van der Slujis, B., Dickson, G., van Engelen, B., Vissing, John & Raz, V., 1 Oct 2016, In: Human Molecular Genetics. 25, 19, p. 4282-4287 6 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
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation
Karazi, W., Scalco, R. S., Stemmerik, M. G., Løkken, N., Lucia, A., Santalla, A., Martinuzzi, A., Vavla, M., Reni, G., Toscano, A., Musumeci, O., Kouwenberg, C. V., Laforêt, P., Millán, B. S., Vieitez, I., Siciliano, G., Kühnle, E., Trost, R., Sacconi, S., Durmus, H. & 9 others, , 2023, In: Orphanet Journal of Rare Diseases. 18, 9 p., 210.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)
Scalco, R. S., Lucia, A., Santalla, A., Martinuzzi, A., Vavla, M., Reni, G., Toscano, A., Musumeci, O., Voermans, N. C., Kouwenberg, C. V., Laforêt, P., San-Millán, B., Vieitez, I., Siciliano, G., Kühnle, E., Trost, R., Sacconi, S., Stemmerik, M. G., Durmus, H., Kierdaszuk, B. & 7 others, , 2020, In: Orphanet Journal of Rare Diseases. 15, 1, p. 330Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Decreased Variability of the 6-Minute Walk Test by Heart Rate Correction in Patients with Neuromuscular Disease
Prahm, K. P., Witting, N. & Vissing, John, 2014, In: PLOS ONE. 9, 12, p. 1-8 8 p., e114273.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deep morphological analysis of muscle biopsies from type III glycogenesis (GSDIII), debranching enzyme deficiency, revealed stereotyped vacuolar myopathy and autophagy impairment
Laforêt, P., Inoue, M., Goillot, E., Lefeuvre, C., Cagin, U., Streichenberger, N., Leonard-Louis, S., Brochier, G., Madelaine, A., Labasse, C., Hedberg-Oldfors, C., Krag, T., Jauze, L., Fabregue, J., Labrune, P., Milisenda, J., Nadaj-Pakleza, A., Sacconi, S., Mingozzi, F., Ronzitti, G. & 7 others, , 2019, In: Acta Neuropathologica Communications. 7, 16 p., 167.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging
Giacomucci, G., Monforte, M., Diaz-Manera, J., Mul, K., Fernandez Torrón, R., Maggi, L., Marini Bettolo, C., Dahlqvist, J. R., Haberlova, J., Camaño, P., Gros, M., Tartaglione, T., Cristiano, L., Gerevini, S., Calandra, P., Deidda, G., Giardina, E., Sacconi, S., Straub, V., Vissing, J. & 3 others, , 2020, In: European Journal of Neurology. 27, 12, p. 2604-2615 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Defekter i den neuromuskulære transmission.
Vissing, John & Paulson, O. B., 2010, Klinisk neurologi og neurokirurgi. 5 ed. København, p. 615-621 6 p.Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Education
- Published
Delayed diagnosis of oculopharyngeal muscular dystrophy in Denmark: from initial ptosis to genetic testing
Mensah, A., Witting, N., Duno, M., Milea, D. & Vissing, John, 2014, In: Acta Ophthamologica (Online). 92, 3, p. e247-e249Research output: Contribution to journal › Comment/debate › Research › peer-review
- Published
Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotype
Witting, N., Duno, M. & Vissing, John, 2011, In: Acta Myologica. 30, 3, p. 182-4 3 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Depletion of ATP Limits Membrane Excitability of Skeletal Muscle by Increasing Both ClC1-Open Probability and Membrane Conductance
Leermakers, P. A., Dybdahl, K. L. T., Husted, K. S., Riisager, A., de Paoli, F. V., Pinós, T., Vissing, John, Krag, T. O. B. & Pedersen, T. H., 2020, In: Frontiers in Neurology. 11, 541.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Deregulation of the ubiquitin-proteasome system is the predominant molecular pathology in OPMD animal models and patients
Anvar, S. Y., hoen, P. A., Venema, A., van der Sluijs, B., van Engelen, B., Snoeck, M., Vissing, John, Trollet, C., Dickson, G., Chartier, A., Simonelig, M., van Ommen, G. B., van der Maarel, S. M. & Raz, V., 2011, In: Skeletal Muscle. 1, 1, p. 15Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Design of Reach: Phase 3 randomized, double-blind, placebo-controlled, 48-week study of the efficacy and safety of losmapimod in FSHD
Tawil, R., Han, J., Wang, L., Vissing, John, van Engelen, B., Statland, J., Mellion, M., Shoskes, J., Morabito, C., Jiang, J. & Webster, J., 2022, In: Neuromuscular Disorders. 32, Supplement 1, p. S104-S104 1 p., P.136 .Research output: Contribution to journal › Conference abstract in journal › Research › peer-review
- Published
Det komplekse kliniske billede ved arvelige mitokondriesygdomme
Frederiksen, A. L., Nielsen, M. F., Yderstræde, K. & Vissing, John, 15 Sep 2014, In: Ugeskrift for Laeger. 176, 38, p. 1779-1783 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness
Johnson, K., Bertoli, M., Phillips, L., Töpf, A., Van den Bergh, P., Vissing, J., Witting, N., Nafissi, S., Jamal-Omidi, S., Łusakowska, A., Kostera-Pruszczyk, A., Potulska-Chromik, A., Deconinck, N., Wallgren-Pettersson, C., Strang-Karlsson, S., Colomer, J., Claeys, K. G., De Ridder, W., Baets, J., von der Hagen, M. & 12 others, , 2018, In: Skeletal Muscle. 8, 12 p., 23.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 915367
Most downloads
-
245
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