John Vissing
Clinical Professor
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160th ENMC International Workshop (First ENMC practical care workshop) Exercise training in patients with muscle diseases: 20-22 June 2008, Naarden, The Netherlands
Vissing, John & van Engelen, B. G. M., 2013, In: Neuromuscular Disorders. 23, 2, p. 182-7 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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162nd ENMC International Workshop: Disorders of muscle lipid metabolism in adults 28-30 November 2008, Bussum, The Netherlands
Laforêt, P., Vianey-Saban, C. & Vissing, John, 1 Apr 2010, In: Neuromuscular Disorders. 20, 4, p. 283-9 7 p.Research output: Contribution to journal › Journal article › Research › peer-review
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188th ENMC International Workshop: Inclusion Body Myositis, 2–4 December 2011, Naarden, The Netherlands
Rose, M. R., Group, E. I. W. & Vissing, John, 2013, In: Neuromuscular Disorders. 23, 12, p. 1044-1055 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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1st International Workshop on Clinical trial readiness for sarcoglycanopathies 15-16 November 2016, Evry, France
Sarcoglycanopathies Working Group, S. W. G., 2017, In: Neuromuscular Disorders. 27, 7, p. 683-692Research output: Contribution to journal › Conference article › Research
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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
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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
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222nd ENMC International Workshop: Myotonic dystrophy, developing a European consortium for care and therapy, Naarden, The Netherlands, 1-2 July 2016
Wood, L., Bassez, G., van Engelen, B., Lochmüller, H., Schoser, B., 222nd ENMC workshop participants, 2. E. W. P., Atalaiae, A., Balabanovf, P., Bassez, G., Treweek, S., Vissing, John & Wood, L., 2018, In: Neuromuscular Disorders. 28, 5, p. 463-469Research output: Contribution to journal › Comment/debate › Research
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229th ENMC international workshop: Limb girdle muscular dystrophies - Nomenclature and reformed classification Naarden, the Netherlands, 17-19 March 2017
Straub, V., Murphy, A., Udd, B., LGMD workshop study group, L. W. S. G., Angelini, C., Aymé, S., Bönnemann, C., Urtizberea, A., Vissing, John & Walter, M., 2018, In: Neuromuscular Disorders. 28, 8, p. 702-710Research output: Contribution to journal › Comment/debate › Research
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233rd ENMC International Workshop: Clinical Trial Readiness for Calpainopathies, Naarden, The Netherlands, 15-17 September 2017
Lostal, W., Urtizberea, J. A., Richard, I., calpain 3 study group, C. 3. S. G., Alonso-Jiménez, A., Carlier, R., Carson, V., Vainzof, M., Vissing, John & Walter, M., 2018, In: Neuromuscular Disorders. 28, 6, p. 540-549Research output: Contribution to journal › Comment/debate › Research
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251st ENMC international workshop: Polyglucosan storage myopathies 13–15 December 2019, Hoofddorp, the Netherlands
Laforêt, P., Oldfors, A., Malfatti, E., Vissing, J., Colle, M. A., Duran, J., Gentry, M., Guinovart, J., Hurley, T., Kakhlon, O., Krag, T., Landy, H., Lilleør, C. B., Minassian, B., Mingozzi, F., Murphy, E., Piercy, R., Piraud, M., Ramanan, V., Stemmerik, M. & 3 others, , 2021, In: Neuromuscular Disorders. 31, 5, p. 466-477 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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254th ENMC international workshop. Formation of a European network to initiate a European data collection, along with development and sharing of treatment guidelines for adult SMA patients. Virtual meeting 28 – 30 January 2022
254th ENMC Workshop Study Group, 2. E. W. S. G., 2023, In: Neuromuscular Disorders. 33, 6, p. 511-522 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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263rd ENMC International Workshop: Focus on female carriers of dystrophinopathy: refining recommendations for prevention, diagnosis, surveillance, and treatment. Hoofddorp, The Netherlands, 13-15 May 2022
Sarkozy, A., Quinlivan, R., Bourke, J. P., Ferlini, A., Barthélémy, I., Cripe, L. H., Reuben, E., Evangelista, T., Florian, A., Gribnau, J., Gonzalez-Quereda, L., Guglieri, M., Niks, E., Phadke, R., Politano, L., Quinlivan, R., Vissing, J., Voermans, N., Vroom, E., Pietrusz, A. & 3 others, , 2023, In: Neuromuscular Disorders. 33, 3, p. 274-284 11 p.Research output: Contribution to journal › Conference article › Research › peer-review
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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
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265th ENMC International Workshop: Muscle imaging in Facioscapulohumeral Muscular Dystrophy (FSHD): relevance for clinical trials. 22–24 April 2022, Hoofddorp, The Netherlands
Monforte, M., Attarian, S., Vissing, John, Diaz-Manera, J., Tasca, G. & 265th ENMC workshop participants, 2. E. W. P., 2023, In: Neuromuscular Disorders. 33, 1, p. 65-75 11 p.Research output: Contribution to journal › Journal article › Communication
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31P-MRS of skeletal muscle is not a sensitive diagnostic test for mitochondrial myopathy.
Dysgaard, Tina, Quistorff, B., Wibrand, F. & Vissing, John, 2007, In: Journal of Neurology. 254, 1, p. 29-37 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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BAG3 myopathy is not always associated with cardiomyopathy
Andersen, A. G., Fornander, F., Schrøder, H. D., Krag, T., Straub, V., Duno, M. & Vissing, John, 2018, In: Neuromuscular Disorders. 28, 9, p. 798-801Research output: Contribution to journal › Journal article › Research › peer-review
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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
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NEB mutations disrupt the super-relaxed state of myosin and remodel the muscle metabolic proteome in nemaline myopathy
Ranu, N., Laitila, J., Dugdale, H. F., Mariano, J., Kolb, J. S., Wallgren-Pettersson, C., Witting, N., Vissing, J., Vilchez, J. J., Fiorillo, C., Zanoteli, E., Auranen, M., Jokela, M., Tasca, G., Claeys, K. G., Voermans, N. C., Palmio, J., Huovinen, S., Moggio, M., Beck, T. N. & 3 others, , 2022, In: Acta Neuropathologica Communications. 10, 185.Research output: Contribution to journal › Journal article › Research › peer-review
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Nampt controls skeletal muscle development by maintaining Ca2+ homeostasis and mitochondrial integrity
Basse, A. L., Agerholm, M., Farup, J., Dalbram, E., Nielsen, J., Ørtenblad, N., Altıntaş, A., Ehrlich, A. M., Krag, T., Bruzzone, S., Dall, M., de Guia, R. M., Jensen, J. B., Møller, A. B., Karlsen, A., Kjær, M., Barrès, R., Vissing, J., Larsen, S., Jessen, N. & 1 others, , 2021, In: Molecular Metabolism. 53, 101271.Research output: Contribution to journal › Journal article › Research › peer-review
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POPDC3 Gene Variants Associate with a New Form of Limb Girdle Muscular Dystrophy
Vissing, John, Johnson, K., Töpf, A., Nafissi, S., Díaz-Manera, J., French, V. M., Schindler, R. F., Sarathchandra, P., Løkken, N., Rinné, S., Freund, M., Decher, N., Müller, T., Duno, M., Krag, T., Brand, T. & Straub, V., Dec 2019, In: Annals of Neurology. 86, 6, p. 832-843 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A New Glycogen Storage Disease Caused by a Dominant PYGM Mutation
Echaniz-Laguna, A., Lornage, X., Laforêt, P., Orngreen, M. C., Edelweiss, E., Brochier, G., Bui, M. T., Silva-Rojas, R., Birck, C., Lannes, B., Romero, N. B., Vissing, John, Laporte, J. & Böhm, J., 2020, In: Annals of Neurology. 88, 2, p. 274-282Research output: Contribution to journal › Journal article › Research › peer-review
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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
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A decline in PABPN1 induces progressive muscle weakness in oculopharyngeal muscle dystrophy and in muscle aging
Anvar, S. Y., Raz, Y., Verway, N., van der Sluijs, B., Venema, A., Goeman, J. J., Vissing, John, van der Maarel, S. M., 't Hoen, P. A. C., van Engelen, B. G. M. & Raz, V., 2013, In: Aging. 5, 6, p. 412-26 15 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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
ID: 915367
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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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Aerobic Training in Patients with Congenital Myopathy
Research output: Contribution to journal › Journal article › Research › peer-review
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