The assessment of fatigue: Psychometric qualities and norms for the Checklist individual strength von Worm-Smeitink, M, Gielissen, M, Bloot, L, van Laarhoven, H.W.M, van Engelen, B.G.M, van Riel, P, Bleijenberg, G, Nikolaus, S, Knoop, H

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Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis von Lilleker, JB, Rietveld, A, Pye, SR, Mariampillai, K, Benveniste, O, Peeters, MTJ, Miller, JAL, Hanna, MG, Machado, PM, Parton, MJ, Gheorghe, KR, Badrising, UA, Lundberg, IE, Sacconi, S, Herbert, MK, McHugh, NJ, Lecky, BRF, Brierley, C, Hilton-Jones, D, Lamb, JA, Roberts, ME, Cooper, RG, Saris, CGJ, Pruijn, GJM, Chinoy, H, van Engelen, BGM

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Fatigue, not self-rated motor symptom severity, affects quality of life in functional motor disorders von Gelauff, J. M., Kingma, E. M., Kalkman, J. S., Bezemer, R., van Engelen, B. G. M., Stone, J., Tijssen, M. A. J., Rosmalen, J. G. M.

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RYR1-related myopathies: a wide spectrum of phenotypes throughout life von Snoeck, M., van Engelen, B. G. M., Küsters, B., Lammens, M., Meijer, R., Molenaar, J. P. F., Raaphorst, J., Verschuuren-Bemelmans, C. C., Straathof, C. S. M., Sie, L. T. L., de Coo, I. F., van der Pol, W. L., de Visser, M., Scheffer, H., Treves, S., Jungbluth, H., Voermans, N. C., Kamsteeg, E.-J.

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Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy von CATS, E. A, VAN DER POL, W.-L, WOKKE, J. H, VELDINK, J. H, VAN DEN BERG, L. H, PIEPERS, S, FRANSSEN, H, JACOBS, B. C, VAN DEN BERG-VOS, R. M, KUKS, J. B, VAN DOORN, P. A, VAN ENGELEN, B. G, VERSCHUUREN, J. J

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Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients von Demirdas, S., Dulfer, E., Robert, L., Kempers, M., van Beek, D., Micha, D., van Engelen, B.G., Hamel, B., Schalkwijk, J., Loeys, B., Maugeri, A., Voermans, N.C.

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Clinical features of facioscapulohumeral muscular dystrophy 2 von DE GREEF, J. C, LEMMERS, R. J. L. F, DESNUELLE, C, SPULER, S, TARNOPOLSKY, M, VENANCE, S. L, FRANTS, R. R, VAN DER MAAREL, S. M, TAWIL, R, CAMANO, P, DAY, J. W, SACCONI, S, DUNAND, M, VAN ENGELEN, B. G. M, KIURU-ENARI, S, PADBERG, G. W, ROSA, A. L

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Establishing the role of muscle ultrasound as an imaging biomarker in facioscapulohumeral muscular dystrophy von Vincenten, S C C, Teeselink, S, Voermans, N C, van Engelen, B G M, Mul, K, van Alfen, N

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Clinical neurophysiology of fatigue von Zwarts, M.J, Bleijenberg, G, van Engelen, B.G.M

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Anti-signal recognition particle autoantibodies: marker of a necrotising myopathy von Hengstman, G J D, ter Laak, H J, Vree Egberts, W T M, Lundberg, I E, Moutsopoulos, H M, Vencovsky, J, Doria, A, Mosca, M, van Venrooij, W J, van Engelen, B G M

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Evaluation of blood gene expression levels in facioscapulohumeral muscular dystrophy patients von Signorelli, M., Mason, A. G., Mul, K., Evangelista, T., Mei, H., Voermans, N., Tapscott, S. J., Tsonaka, R., van Engelen, B. G. M., van der Maarel, S. M., Spitali, P.

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The predictive value of respiratory function tests for non-invasive ventilation in amyotrophic lateral sclerosis von Tilanus, T B M, Groothuis, J T, TenBroek-Pastoor, J M C, Feuth, T B, Heijdra, Y F, Slenders, J P L, Doorduin, J, Van Engelen, B G, Kampelmacher, M J, Raaphorst, J

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Characterizing the face in facioscapulohumeral muscular dystrophy von Loonen, T. G. J., Horlings, C. G. C., Vincenten, S. C. C., Beurskens, C. H. G., Knuijt, S., Padberg, G. W. A. M., Statland, J. M., Voermans, N. C., Maal, T. J. J., van Engelen, B. G. M., Mul, K.

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Prevalence and mutation spectrum of skeletal muscle channelopathies in the Netherlands von Stunnenberg, B.C., Raaphorst, J., Deenen, J.C.W., Links, T.P., Wilde, A.A., Verbove, D.J., Kamsteeg, E.J., van den Wijngaard, A., Faber, C.G., van der Wilt, G.J., van Engelen, B.G.M., Drost, G., Ginjaar, H.B.

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Evaluation of prednisolone treatment in the acute phase of neuralgic amyotrophy: an observational study von van Eijk, J J J, van Alfen, N, Berrevoets, M, van der Wilt, G J, Pillen, S, van Engelen, B G M

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Redefining the clinical phenotypes of non-dystrophic myotonic syndromes von Trip, J, Drost, G, Ginjaar, H B, Nieman, F H M, van der Kooi, A J, de Visser, M, van Engelen, B G M, Faber, C G

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Relation between muscle fiber conduction velocity and fiber size in neuromuscular disorders von Blijham, P. J, ter Laak, H. J, Schelhaas, H. J, van Engelen, B. G. M, Stegeman, D. F, Zwarts, M. J

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Having an eye for myotonic dystrophy: A qualitative study on experiences and support needs in myotonic dystrophy type 1 patients with a diagnostic delay after early-onset cataract von Karnebeek, I.E.A., Boon, H.T.M., Huis, A.M.P., Cup, E.H.C., Eggink, C.A., Schouten, M.I., van der Looij, H.J., van Engelen, B.G.M., Smulders, F.H.P., Voermans, N.C.

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Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham’s razor to its various features von Padberg, G.W., van Engelen, B.G.M., Voermans, N.C.

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Deep phenotyping of facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging von Giacomucci, G., Monforte, M., Diaz‐Manera, J., Mul, K., Fernandez Torrón, R., Maggi, L., Marini Bettolo, C., Dahlqvist, J. R., Haberlova, J., Camaño, P., Gros, M., Tartaglione, T., Cristiano, L., Gerevini, S., Calandra, P., Deidda, G., Giardina, E., Sacconi, S., Straub, V., Vissing, J., Van Engelen, B., Ricci, E., Tasca, G.

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