Experienced fatigue in facioscapulohumeral dystrophy, myotonic dystrophy, and HMSN-I von Kalkman, J S, Schillings, M L, van der Werf, S P, Padberg, G W, Zwarts, M J, van Engelen, B G M, Bleijenberg, G

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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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1st FSHD European Trial Network workshop:Working towards trial readiness across Europe von Voermans, N.C., Vriens-Munoz Bravo, M., Padberg, G.W., Laforêt, P., van Alfen, N., Attarian, S., Badrising, U.A., Bugiardini, E., González, P. Camano, Carlier, R.Y., Desguerre, I., Diaz-Manera, J., Dumonceaux, J., van Engelen, B.G., Evangelista, T., Khosla, S., de Munain, A. López, van der Maarel, S.M., Mejat, A., Monforte, M., Montagnese, F., Mul, K., Oflazer, P., Porter, B., Quijano-Roy, S., Ricci, E., Sacconi, S., Sansone, V.A., Schoser, B., Statland, J., Stumpe, E., Tasca, G., Tawil, R., Turner, C., Vissing, J.

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Strength training and albuterol in facioscapulohumeral muscular dystrophy von VAN DER KOOI, E. L, VOGELS, O. J. M, VAN ASSELDONK, R. J. G. P, LINDEMAN, E, HENDRIKS, J. C. M, WOHLGEMUTH, M, VAN DER MAAREL, S. M, PADBERG, G. W

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Epidemiology and pathophysiology of falls in facioscapulohumeral disease von Horlings, C G C, Munneke, M, Bickerstaffe, A, Laverman, L, Allum, J H J, Padberg, G W A M, Bloem, B R, van Engelen, B G M

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Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD von DE GREEF, J. C, WOHLGEMUTH, M, CHAN, O. A, HANSSON, K. B, SMEETS, D, FRANTS, R. R, WEEMAES, C. M, PADBERG, G. W, VAN DER MAAREL, S. M

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Limb-girdle muscular dystrophy in the Netherlands : Gene defect identified in half the families von VAN DER KOOI, A. J, FRANKHUIZEN, W. S, BAKKER, E, GINJAAR, H. B, BARTH, P. G, HOWELER, C. J, PADBERG, G. W, SPAANS, F, WINTZEN, A. R, WOKKE, J. H. J, VAN OMMEN, G.-J. B, DE VISSER, M

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FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients von Rijkers, T, Deidda, G, van Koningsbruggen, S, van Geel, M, Lemmers, R J L F, van Deutekom, J C T, Figlewicz, D, Hewitt, J E, Padberg, G W, Frants, R R, van der Maarel, S M

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Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family von de Kovel, C G F, Hol, F A, Heister, J G A M, Willemen, J J H T, Sandkuijl, L A, Franke, B, Padberg, G W

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The neuropathology of hereditary congenital facial palsy vs Möbius syndrome von VERZIJL, H. T. F. M, VAN DER ZWAAG, B, LAMMENS, M, TEN DONKELAAR, H. J, PADBERG, G. W

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Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element von Gabriëls, J, Beckers, M.-C, Ding, H, De Vriese, A, Plaisance, S, van der Maarel, S.M, Padberg, G.W, Frants, R.R, Hewitt, J.E, Collen, D, Belayew, A

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Effects of training and albuterol on pain and fatigue in facioscapulohumeral muscular dystrophy von VAN DER KOOI, E. L, KALKMAN, J. S, LINDEMAN, E, HENDRIKS, J. C. M, VAN ENGELEN, B. G. M, BLEIJENBERG, G, PADBERG, G. W

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213th ENMC International Workshop: Outcome measures and clinical trial readiness in idiopathic inflammatory myopathies, Heemskerk, The Netherlands, 18–20 September 2015 von Benveniste, Olivier, Rider, Lisa G., Aggarwal, R., Allenbach, Y., Benveniste, O., De Bleecker, J.L., de Groot, I., Devilliers, H., Hilton-Jones, D., Hogrel, J.-Y., Lundberg, I.E., Mammen, A.L., Oakley, Oddis, C., Padberg, G., Ponce, D., Rider, L.G., Rose, M.R., Sanner, H., Selva- O'Callaghan, A., de Visser, M., Wells, A., Werth, V.P.

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High specificity of myositis specific autoantibodies for myositis compared with other neuromuscular disorders von HENGSTMAN, G. J. D, VAN BRENK, L, VREE EGBERTS, W. T. M, VAN DER KOOI, E. L, BORM, G. F, PADBERG, G. W. A. M, VAN VENROOIJ, W. J, VAN ENGELEN, B. G. M

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Only fat infiltrated muscles in resting lower leg of FSHD patients show disturbed energy metabolism von Kan, H. E., Klomp, D. W. J., Wohlgemuth, M., van Loosbroek-Wagemans, I., van Engelen, B. G. M., Padberg, G. W., Heerschap, A.

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Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere von van der Maarel, Silvère M, Lemmers, Richard J.L.F, de Kievit, Peggy, Sandkuijl, Lodewijk, Padberg, George W, van Ommen, Gert-Jan B, Frants, Rune R

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Localization of the gene for Cowden disease to chromosome 10q22-23 von Nelen, M.R, Padberg, G.W, Peeters, E.A.J, Lin, A.Y, Helm, B. van den, Frants, R.R, Goulon, V, Goldstein, A.M, Reen, M.M.M van, Eastern, D.F, Eeles, R.A, Hodgson, S, Mulvihill, J.J, Murday, V.A, Tucker, M.A, Mariman, E.C.M, Starink, T.M, Ponder, B.A.J, Ropers, H.H, Kremer, H, Longy, M, Eng, C

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Face mask spirometry and respiratory pressures in normal subjects von Wohlgemuth, M, van der Kooi, E.L, Hendriks, J.C, Padberg, G.W, Folgering, H.T

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The choice of treatment of single brain metastasis should be based on extracranial tumor activity and age von Noordijk, Evert M., Vecht, Charles J., Haaxma-Reiche, Hanny, Padberg, George W., Voormolen, Joan H.C., Hoekstra, Foppe H., Tans, Joseph Th.J., Lambooij, Nanno, Metsaars, Jan A.L., Wattendorff, A.Rolf, Brand, Ronald, Hermans, Jo

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A Second Gene for Autosomal Dominant Möbius Syndrome Is Localized to Chromosome 10q, in a Dutch Family von Verzijl, H.T.F.M., van den Helm, B., Veldman, B., Hamel, B.C.J., Kuyt, L.P., Padberg, G.W., Kremer, H.

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