Frequency and Phenotype of Myotubular Myopathy Amongst Danish Patients with Congenital Myopathy Older than 5 Years

por Werlauff, U., Petri, H., Witting, N., Vissing, J.
Publicado 2015

Mitochondrial dysfunction and risk of cancer

por Lund, M, Melbye, M, Diaz, L J, Duno, M, Wohlfahrt, J, Vissing, J
Publicado 2015

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

por 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, J.
Publicado 2016

Low aerobic capacity in McArdle disease: A role for mitochondrial network impairment?

por Villarreal-Salazar, M., Santalla, A., Real-Martínez, A., Nogales-Gadea, G., Valenzuela, P.L., Fiuza-Luces, C., Andreu, A.L., Rodríguez-Aguilera, J.C., Martín, M.A., Arenas, J., Vissing, J., Lucia, A., Krag, T.O., Pinós, T.
Publicado 2022

MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement

por Donkervoort, S., Sabouny, R., Yun, P., Gauquelin, L., Chao, K. R., Hu, Y., Al Khatib, I., Töpf, A., Mohassel, P., Cummings, B. B., Kaur, R., Saade, D., Moore, S. A., Waddell, L. B., Farrar, M. A., Goodrich, J. K., Uapinyoying, P., Chan, S.H. S., Javed, A., Leach, M. E., Karachunski, P., Dalton, J., Medne, L., Harper, A., Thompson, C., Thiffault, I., Specht, S., Lamont, R. E., Saunders, C., Racher, H., Bernier, F. P., Mowat, D., Witting, N., Vissing, J., Hanson, R., Coffman, K. A., Hainlen, M., Parboosingh, J. S., Carnevale, A., Yoon, G., Schnur, R. E., Boycott, K. M., Mah, J. K., Straub, V., Foley, A. Reghan, Innes, A. M., Bönnemann, C. G., Shutt, T. E.
Publicado 2019