John Vissing

John Vissing

Clinical Professor

Member of:

  • Neurology


Publication year:
All
1 - 10 out of 34Page size: 10
  1. 2019
  2. Published

    Muscle MRI in a large cohort of patients with oculopharyngeal muscular dystrophy

    Alonso-Jimenez, A., Kroon, R. H. M. J. M., Alejaldre-Monforte, A., Nuñez-Peralta, C., Horlings, C. G. C., van Engelen, B. G. M., Olivé, M., González, L., Verges-Gil, E., Paradas, C., Márquez, C., Garibaldi, M., Gallano, P., Rodriguez, M. J., Gonzalez-Quereda, L., Dominguez Gonzalez, C., Vissing, J., Fornander, F., Eisum, A-S. V., García-Sobrino, T. & 30 others, Pardo, J., García-Figueiras, R., Muelas, N., Vilchez, J. J., Kapetanovic, S., Tasca, G., Monforte, M., Ricci, E., Gomez, M. T., Bevilacqua, J. A., Diaz-Jara, J., Zamorano, I. I., Carlier, R. Y., Laforet, P., Pelayo-Negro, A., Ramos-Fransi, A., Martínez, A., Marini-Bettolo, C., Straub, V., Gutiérrez, G., Stojkovic, T., Martín, M. A., Morís, G., Fernández-Torrón, R., Lopez De Munaín, A., Cortes-Vicente, E., Querol, L., Rojas-García, R., Illa, I. & Diaz-Manera, J., May 2019, In: Journal of neurology, neurosurgery, and psychiatry. 90, 5, p. 576-585 10 p.

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

  3. Published

    Eculizumab improves fatigue in refractory generalized myasthenia gravis

    Andersen, H., Mantegazza, R., Wang, J. J., O’Brien, F., Patra, K., Howard, J. F., The REGAIN Study Group, T. R. S. G., Mazia, C. G., Wilken, M., Barroso, F., Vissing, John, Højgaard, J., Witting, N., Autzen, A. O., Pedersen, J., Yang, I., Nye, J. & Vu, H., Mar 2019, In: Quality of Life Research. 28, p. 2247-2254

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

  4. Published

    Aberrant regulation of epigenetic modifiers contributes to the pathogenesis in patients with selenoprotein N-related myopathies

    Bachmann, C., Noreen, F., Voermans, N. C., Schär, P. L., Vissing, John, Fock, J. M., Bulk, S., Kusters, B., Moore, S. A., Beggs, A. H., Mathews, K. D., Meyer, M., Genetti, C. A., Meola, G., Cardani, R., Mathews, E., Jungbluth, H., Muntoni, F., Zorzato, F. & Treves, S., Jul 2019, In: Human Mutation. 40, 7, p. 962-974 13 p.

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

  5. Published

    Expanding the phenotype of filamin-C-related myofibrillar myopathy

    Borch, J. D. S., Eisum, A. S. V., Krag, T. & Vissing, John, 2019, In: Clinical Neurology and Neurosurgery. 176, p. 30-33 4 p.

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

  6. Published

    MYO-MRI diagnostic protocols in genetic myopathies

    Chardon, J. W., Díaz-Manera, J., Tasca, G., Bönnemann, C. G., Gómez-Andrés, D., Heerschap, A., Mercuri, E., Muntoni, F., Pichiecchio, A., Ricci, E., Walter, M. C., Hanna, M., Jungbluth, H., Morrow, J. M., Torrón, R. F., Udd, B., Vissing, J., Yousry, T., Quijano-Roy, S., Straub, V. & 2 others, Carlier, R. Y. & MYO-MRI Working Group, M. W. G., Nov 2019, In: Neuromuscular Disorders. 29, 11, p. 827-841

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

  7. Published

    Refining the spinobulbar muscular atrophy phenotype by quantitative MRI and clinical assessments

    Dahlqvist, J. R., Oestergaard, S. T., Poulsen, N. S., Thomsen, C. & Vissing, John, 2019, In: Neurology. 92, 6, p. e548-e559

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

  8. Published

    Relationship between muscle inflammation and fat replacement assessed by MRI in facioscapulohumeral muscular dystrophy

    Dahlqvist, J. R., Andersen, G., Khawajazada, T., Vissing, C., Thomsen, C. & Vissing, John, May 2019, In: Journal of Neurology. 266, 5, p. 1127-1135 9 p.

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

  9. Published

    Muscle contractility in spinobulbar muscular atrophy

    Dahlqvist, J. R., Oestergaard, S. T., Poulsen, N. S., Knak, K. L., Thomsen, C. & Vissing, John, 2019, In: Scientific Reports. 9, 1, 8 p., 4680.

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

  10. 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

  11. Published

    Adaptations in mitochondrial enzymatic activity occurs independent of genomic dosage in response to aerobic exercise training and deconditioning in human skeletal muscle

    Fritzen, Andreas Mæchel, Thøgersen, F. B., Thybo, K., Vissing, C. R., Krag, T. O., Ruiz-Ruiz, C., Risom, L., Wibrand, F., Høeg, L. D., Kiens, Bente, Duno, M., Vissing, John & Jeppesen, T. D., 2019, In: Cells. 8, 3, 16 p., 237.

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

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ID: 915367