Spondylodiscitis complicated with an epidural abscess due to Shewanella Algae: A case report von Nassafi, E.M., Remiche, V., Ionicioiu, A., Delvallee, M.

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Fat embolism syndrome and massive middle cerebral artery occlusion: a case report von Wattiaux, B, Carlier, M, Vanacker, P, Remiche, V, Vanderweerden, G

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MYASTHENIA & RELATED DISORDERS: P.38 Autosomal recessive inheritance in hypokalaemic periodic paralysis due to a homozygous SCN4A gene mutation von Remiche, G., Desmyter, L., Grenet, M., Vandernoot, I., Devuyst, O., Smits, G., Potmans, V.

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MYASTHENIA & RELATED DISORDERS von Remiche, G., Desmyter, L., Grenet, M., Vandernoot, I., Devuyst, O., Smits, G., Potmans, V.

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P252 Exploration of muscle MR imaging and clinical outcome measures in adults with Becker muscular dystrophy von De Wel, B., Iterbeke, L., Huysmans, L., Peeters, R., Goosens, V., Ghysels, S., Byloos, K., Putzeys, G., Dubuisson, N., van den Bergh, P., Van Parijs, V., Remiche, G., Maes, F., Dupont, P., Claeys, K.

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HEREDITARY NEUROPATHIES & ALS: P.105 An unusual clinical presentation of CTBP1-related syndrome associating muscle dystrophy, cerebellar ataxia and paralytic ileus von Houwayek, E. El, Coppens, S., Topf, A., Duff, J., Kaleeta, J., Kadhim, H., Remiche, G., Straub, V., Deconinck, N.

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HEREDITARY NEUROPATHIES & ALS von Houwayek, E. El, Coppens, S., Topf, A., Duff, J., Kaleeta, J., Kadhim, H., Remiche, G., Straub, V., Deconinck, N.

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Belgian retrospective survey of hereditary transthyretin-mediated (hATTR) amyloidosis patients treated with patisiran in real-world practice von Tilleux, S, De Bleecker, Jan, Claeys, K, Destanche, S, Van Parys, V, Baets, Jonathan, Remiche, G

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Supplementary Material for: A first case of acute flaccid myelitis related to enterovirus D-68 in Belgium von M., Rodesch, C., Sculier, V., Lolli, G., Remiche, I., Delpire, C., Fricx, F., Vermeulen, F., Christiaens

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Telemedicine in neuromuscular diseases during COVID-19 pandemic: ERN-NMD European survey von El-Hassar, L., Amara, A., Sanson, B., Lacatus, O., Belhouchet, A.A., Kroneman, M., Claeys, K., Plançon, J.P., Rodolico, C., Primiano, G., Trojsi, F., Filosto, M., Mongini, T.E., Bortolani, S., Monforte, M., Carraro, E., Maggi, L., Ricci, F., Silani, V., Orsucci, D., Créange, A., Péréon, Y., Stojkovic, T., Beek, N.A.M.E. van der, Toscano, A., Pareyson, D., Attarian, S., Bergh, P.Y.K. van den, Remiche, G., Hoeijmakers, J.G.J., Badrising, U., Voermans, N.C., Kaindl, A.M., Schara-Schmidt, U., Schoser, B., Gazzerro, E., Haberlová, J., Vohánka, S., Pál, E., Molnar, M.J., Leonardis, L., Tournev, I.L., Osorio, A.N., Olivé, M., Muelas, N., Alonso-Perez, J., Plá, F., Visser, M. de, Siciliano, G., Sacconi, S.

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Exploration of muscle MR imaging and clinical outcome measures in adults with Becker muscular dystrophy von De Wel, B, Iterbeke, L, Huysmans, L, Peeters, R, Goosens, V, Ghysels, S, Byloos, K, Putzeys, G, Dubuisson, N, van den Bergh, P, Van Parijs, V, Remiche, G, Maes, F, Dupont, P, Claeys, K

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