John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


Publication year:
All
201 - 250 out of 354Page size: 50
  1. 2017
  2. 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

  3. 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

  4. 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. 2295-2305

    Research output: Contribution to journal › Journal article › Research › peer-review

  5. 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

  6. Published

    Update on new muscle glycogenosis

    Laforêt, P., Malfatti, E. & Vissing, John, 2017, In: Current Opinion in Neurology. 30, 5, p. 449-456

    Research output: Contribution to journal › Review › Research › peer-review

  7. 2016
  8. Published

    Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T)

    Oestergaard, S. T., Stojkovic, T., Dahlqvist, J. R., Bouchet-Seraphin, C., Nectoux, J., Leturcq, F., Cossée, M., Solé, G., Thomsen, C., Krag, T. O. & Vissing, John, Dec 2016, In: Neurology: Genetics. 2, 6, 7 p., e112.

    Research output: Contribution to journal › Journal article › Research › peer-review

  9. 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

  10. Published

    216th ENMC international workshop: Clinical readiness in FKRP related myopathies January 15-17, 2016 Naarden, The Netherlands

    Richard, I., Laurent, J., Cirak, S., Vissing, John & ENMC FKRP Study Group, E. F. S. G., Oct 2016, In: Neuromuscular Disorders. 26, 10, p. 717-724 8 p.

    Research output: Contribution to journal › Comment/debate › Research

  11. Published

    Exercise training in metabolic myopathies

    Vissing, John, Oct 2016, In: Revue Neurologique. 172, 10, p. 559-565 7 p.

    Research output: Contribution to journal › Review › Research › peer-review

  12. Published

    Limb girdle muscular dystrophies: classification, clinical spectrum and emerging therapies

    Vissing, John, Oct 2016, In: Current Opinion in Neurology. 29, 5, p. 635-641 7 p.

    Research output: Contribution to journal › Review › Research › peer-review

  13. 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

  14. Published

    Differential glucose metabolism in mice and humans affected by McArdle disease

    Krag, T. O., Pinós, T., Nielsen, T. L., Duran, J., García-Rocha, M., Andreu, A. L. & Vissing, John, 1 Aug 2016, In: American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. 311, 2, p. R307-R314

    Research output: Contribution to journal › Journal article › Research › peer-review

  15. Published

    Differential Muscle Involvement in Mice and Humans Affected by McArdle Disease

    Krag, T. O., Pinós, T., Nielsen, T. L., Brull, A., Andreu, A. L. & Vissing, John, May 2016, In: Journal of Neuropathology and Experimental Neurology. 75, 5, p. 441-54 14 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  16. Published

    A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy

    Vissing, John, Barresi, R., Witting, N., Van Ghelue, M., Gammelgaard, L., Bindoff, L. A., Straub, V., Lochmüller, H., Hudson, J., Arnardottir, S., Dahlbom, K., Jonsrud, C. & Duno, M., 30 Apr 2016, In: Brain. 139, 8, p. 2154-2163 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  17. 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

  18. Published

    Prevalence and phenotypes of congenital myopathy due to α-actin 1 gene mutations

    Witting, N., Werlauff, U., Duno, M. & Vissing, John, Mar 2016, In: Muscle & Nerve. 53, 3, p. 388-93 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  19. Published

    Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy

    Pareyson, D., Fratta, P., Pradat, P., Soraru, G., Finsterer, J., Vissing, John, Jokela, M. E., Udd, B., Ludolph, A. C., Sagnelli, A. & Weydt, P., Mar 2016, In: Journal of Molecular Neuroscience. 58, 3, p. 394-400 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  20. Published

    Two- and 6-minute walk tests assess walking capability equally in neuromuscular diseases

    Andersen, L. K., Knak, K. L., Witting, N. & Vissing, John, 2 Feb 2016, In: Neurology. 86, 5, p. 442-5 4 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  21. Published

    Prevalence of migraine in persons with the 3243A>G mutation in mitochondrial DNA

    Guo, S., Esserlind, A., Andersson, Z., Frederiksen, A. L., Olesen, J., Vissing, John & dlt446, dlt446, Jan 2016, In: European Journal of Neurology. 23, 1, p. 175-81 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  22. Published

    Aerobic Training in Patients with Congenital Myopathy

    Hedermann, G., Vissing, C. R., Jensen, K., Preisler, N., Witting, N. & Vissing, John, 2016, In: PLoS ONE. 11, 1, 9 p., e0146036.

    Research output: Contribution to journal › Journal article › Research › peer-review

  23. Published

    Axial myopathy: an overlooked feature of muscle diseases

    Witting, N., Andersen, L. K. & Vissing, John, 2016, In: Brain. 139, 1, p. 13-22 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  24. Published

    Body weight-supported training in Becker and Limb Girdle 2I muscular dystrophy

    Jensen, B. R., Berthelsen, M. P., Husu, E., Christensen, S. B., Prahm, K. P. & Vissing, John, 2016, In: Muscle & Nerve. 54, 2, p. 239-243 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  25. Published

    Effect of Gender, Disease Duration and Treatment on Muscle Strength in Myasthenia Gravis

    Citirak, G., Cejvanovic, S., Andersen, H. & Vissing, John, 2016, In: PLOS ONE. 11, 10, p. 1-14 14 p., e0164092.

    Research output: Contribution to journal › Journal article › Research › peer-review

  26. Published

    Exercise Intolerance and Myoglobinuria Associated with a Novel Maternally Inherited MT-ND1 Mutation

    Rafiq, J., Duno, M., Østergaard, Elsebet, Ravn, K., Vissing, C. R., Wibrand, F. & Vissing, John, 2016, JIMD Reports. Springer, Vol. 25. p. 65-70 (JIMD Reports).

    Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review

  27. Published

    Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy

    Zaharieva, I. T., Thor, M. G., Oates, E. C., van Karnebeek, C., Hendson, G., Blom, E., Witting, N., Rasmussen, M., Gabbett, M. T., Ravenscroft, G., Sframeli, M., Suetterlin, K., Sarkozy, A., D'Argenzio, L., Hartley, L., Matthews, E., Pitt, M., Vissing, J., Ballegaard, M., Krarup, C. & 20 others, Slørdahl, A., Halvorsen, H., Ye, X. C., Zhang, L., Løkken, N., Werlauff, U., Abdelsayed, M., Davis, M. R., Feng, L., Phadke, R., Sewry, C. A., Morgan, J. E., Laing, N. G., Vallance, H., Ruben, P., Hanna, M. G., Lewis, S., Kamsteeg, E., Männikkö, R. & Muntoni, F., 2016, In: Brain. 139, 3, p. 674-91 18 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  28. Published

    Polymyositis following autologous haematopoietic stem cell transplantation

    Hedermann, G., Marquart, H. V. & Vissing, John, 2016, In: Scandinavian Journal of Rheumatology. 45, 5, p. 429-31 3 p.

    Research output: Contribution to journal › Letter › Research › peer-review

  29. 2015
  30. Published

    A New Mouse Model of Limb-Girdle Muscular Dystrophy Type 2I Homozygous for the Common L276I Mutation Mimicking the Mild Phenotype in Humans

    Krag, T. O. & Vissing, John, Dec 2015, In: Journal of Neuropathology and Experimental Neurology. 74, 12, p. 1137-46 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  31. Published

    Muscle imaging in patients with tubular aggregate myopathy caused by mutations in STIM1

    Tasca, G., D'Amico, A., Monforte, M., Nadaj-Pakleza, A., Vialle, M., Fattori, F., Vissing, John, Ricci, E. & Bertini, E., Nov 2015, In: Neuromuscular Disorders. 25, 11, p. 898-903 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  32. Published

    A third case of congenital myasthenic syndrome caused by mutations in SCN4A

    Witting, N., Werlauff, U., Ballegaard, Martin & Vissing, John, Oct 2015, p. S209-S209. 1 p.

    Research output: Contribution to conference › Poster › Research › peer-review

  33. Published

    LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies

    Løkken, N., Born, A. P., Duno, M. & Vissing, John, Oct 2015, In: Muscle & Nerve. 52, 4, p. 547-53 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  34. Published

    Aerobic training and postexercise protein in facioscapulohumeral muscular dystrophy: RCT study

    Andersen, G., Prahm, K. P., Dahlqvist, J. R., Citirak, G. & Vissing, John, Aug 2015, In: Neurology. 85, 5, p. 396-403 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  35. Published

    Lactate and Energy Metabolism During Exercise in Patients With Blocked Glycogenolysis (McArdle Disease)

    Ørngreen, M. C., Jeppesen, T. D., Taivassalo, T., Hauerslev, S., Preisler, N., Heinicke, K., Haller, R. G., Vissing, John & van Hall, Gerrit, Aug 2015, In: Journal of Clinical Endocrinology and Metabolism. 100, 8, p. E1096-E1104 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  36. Published

    Training improves oxidative capacity, but not function, in spinal muscular atrophy type III

    Madsen, K. L., Wils, Regitze Sølling, Preisler, N., Thøgersen, F., Berthelsen, M. P. & Vissing, John, Aug 2015, In: Muscle & Nerve. 52, 2, p. 240–244 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  37. Published

    Differences in genetic defects and morphology of eye- and limb muscles in mitochondrial myopathy

    Levison, L., Dunø, M., Risom, L., Toft, Peter Bjerre & Vissing, John, Jun 2015, In: Acta Ophthalmologica. 93, 4, p. e306-8

    Research output: Contribution to journal › Comment/debate › Research › peer-review

  38. Published

    Exercise in muscle glycogen storage diseases

    Preisler, N. R., Haller, R. G. & Vissing, John, May 2015, In: Journal of Inherited Metabolic Disease. 38, 3, p. 551-63 13 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  39. Published

    Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E

    Semplicini, C., Vissing, John, Dahlqvist, J. R., Stojkovic, T., Bello, L., Witting, N., Duno, M., Leturcq, F., Bertolin, C., D'Ambrosio, P., Eymard, B., Angelini, C., Politano, L., Laforêt, P. & Pegoraro, E., 28 Apr 2015, In: Neurology. 84, 17, p. 1772-81 10 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  40. Published

    Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type III

    Preisler, N., Laforêt, P., Madsen, K. L., Prahm, K. P., Hedermann, G., Vissing, C. R., Galbo, Henrik & Vissing, John, 28 Apr 2015, In: Neurology. 84, 17, p. 1767-71 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  41. Published

    Progression of cardiac involvement in patients with limb-girdle type 2 and Becker muscular dystrophies: a 9-year follow-up study

    Petri, H., Sveen, M., Thune, J. J., Vissing, C., Dahlqvist, J. R., Witting, N., Bundgård, Henning, Køber, Lars Valeur & Vissing, John, 1 Mar 2015, In: International Journal of Cardiology. 182, p. 403-11 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  42. Published

    Clinical and neurophysiological response to pharmacological treatment of DOK7 congenital myasthenia in an older patient

    Witting, N., Crone, C., Duno, M. & Vissing, John, Mar 2015, In: Clinical Neurology and Neurosurgery. 130, p. 168-70 3 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  43. Published

    Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature

    Østergaard, Elsebet, Weraarpachai, W., Ravn, K. J. T., Born, A. P., Jønson, L., Dunø, M., Wibrand, F., Shoubridge, E. A. & Vissing, John, Mar 2015, In: Journal of Medical Genetics. 52, 3, p. 203-7 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  44. Published

    No effect of bezafibrate in patients with CPTII and VLCAD deficiencies

    Ørngreen, M. C., Vissing, John & Laforét, P., Mar 2015, In: Journal of Inherited Metabolic Disease. 38, 2, p. 373-4 2 p.

    Research output: Contribution to journal › Comment/debate › Research › peer-review

  45. Published

    Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover study

    Andersen, G., Ørngreen, M. C., Preisler, N., Jeppesen, T. D., Krag, T. O., Hauerslev, S., van Hall, Gerrit & Vissing, John, 15 Jan 2015, In: American Journal of Physiology: Regulatory, Integrative and Comparative Physiology. 308, 2, p. R123-R130 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  46. Published

    A mitochondrial tRNA(Met) mutation causing developmental delay, exercise intolerance and limb girdle phenotype with onset in early childhood

    Born, A. P., Duno, M., Rafiq, J., Risom, L., Wibrand, F., Østergaard, Elsebet & Vissing, John, Jan 2015, In: European Journal of Paediatric Neurology. 19, 1, p. 69-71 3 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  47. 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

  48. Published

    Mitochondrial dysfunction and risk of cancer

    Lund, M., Melbye, M., Diaz, L. J., Dunø, M., Wohlfahrt, J. & Vissing, John, 2015, In: B J C. 112, 6, p. 1134-40 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  49. 2014
  50. Published

    Effect of sildenafil on skeletal and cardiac muscle in Becker muscular dystrophy

    Witting, N., Kruuse, Christina Rostrup, Nyhuus, B., Prahm, K. P., Citirak, G., Lundgaard, S. J., von Huth, S., Vejlstrup, N., Lindberg, U., Krag, T. O. & Vissing, John, Oct 2014, In: Annals of Neurology. 76, 4, p. 550–557 8 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  51. Published

    Severe paraspinal muscle involvement in facioscapulohumeral muscular dystrophy

    Dahlqvist, J. R., Vissing, C. R., Thomsen, C. & Vissing, John, 23 Sep 2014, In: Neurology. 83, 13, p. 1178-1183 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  52. 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

  53. Published

    Risk of cancer in relatives of patients with myotonic dystrophy: a population-based cohort study

    Lund, M., Diaz, L. J., Gørtz, S., Feenstra, B., Duno, M., Juncker, I., Eiberg, Hans Rudolf Lytchoff, Vissing, John, Wohlfahrt, J. & Melbye, M., Sep 2014, In: European journal of neurology : the official journal of the European Federation of Neurological Societies. 21, 9, p. 1192-1197 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  54. Published

    Cardiac involvement in myotonic dystrophy: a nationwide cohort study

    Lund, M., Diaz, L. J., Ranthe, M. F., Petri, H., Duno, M., Juncker, I., Eiberg, Hans Rudolf Lytchoff, Vissing, John, Bundgaard, H., Wohlfahrt, J. & Melbye, M., 21 Aug 2014, In: European Heart Journal. 35, 32, p. 2158-2164 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

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ID: 915367