Multimorbidity warrants a proactive management of pregnancy in cancer survivors von Kooi, A.‐L. L. F.

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Desmin-related myopathy von van Spaendonck-Zwarts, KY, van Hessem, L, Jongbloed, JDH, de Walle, HEK, Capetanaki, Y, van der Kooi, AJ, van Langen, IM, van den Berg, MP, van Tintelen, JP

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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy von SCHADE VAN WESTRUM, S. M, HOOGERWAARD, E. M, WILDE, A. A. M, DE HAAN, R. J, DE VISSER, M, VAN DER KOOI, A. J, DEKKER, L, STANDAAR, T. S, BAKKER, E, IPPEL, P. F, OOSTERWIJK, J. C, MAJOOR-KRAKAUER, D. F, VAN ESSEN, A. J, LESCHOT, N. J

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Health-related quality of life in Dutch adult survivors of childhood cancer: A nation-wide cohort study von van Erp, L.M.E., Maurice-Stam, H., Kremer, L.C.M., Tissing, W.J.E., van der Pal, H.J.H., de Vries, A.C.H., van den Heuvel-Eibrink, M.M., Versluys, B.A.B., Loonen, J.J., Bresters, D., Louwerens, M., van der Heiden-van der Loo, M., van den Berg, M.H., Ronckers, C.M., van der Kooi, A.L.L.F., van Gorp, M., van Dulmen-den Broeder, E., Grootenhuis, M.A.

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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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Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations von Muchir, A., Medioni, J., Laluc, M., Massart, C., Arimura, T., Kooi, A. J. Van Der, Desguerre, I., Mayer, M., Ferrer, X., Briault, S., Hirano, M., Worman, H. J., Mallet, A., Wehnert, M., Schwartz, K., Bonne, G.

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Treatment-related fertility impairment in long-term female childhood, adolescent and young adult cancer survivors: investigating dose-effect relationships in a European case-contro... von van den Berg, M H, van Dijk, M, Byrne, J, Berger, C, Dirksen, U, Winther, J F, Fossa, S D, Grabow, D, Grandage, V L, Haupt, R, van den Heuvel-Eibrink, M M, Kaiser, M, Kepak, T, van der Kooi, A L F, Kremer, L C M, Kruseova, J, Lambalk, C B, van Leeuwen, F E, Leiper, A, Modan-Moses, D, Spix, C, Twisk, J W R, Ronckers, C M, Kaatsch, P, van Dulmen-den Broeder, E

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Balance control in patients with distal versus proximal muscle weakness von Horlings, C.G.C, Küng, U.M, van Engelen, B.G.M, Voermans, N.C, Hengstman, G.J.D, van der Kooi, A.J, Bloem, B.R, Allum, J.H.J

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Longitudinal follow-up in female Childhood Cancer Survivors: no signs of accelerated ovarian function loss von van der Kooi, A.L.F., van den Heuvel-Eibrink, M.M., van Noortwijk, A., Neggers, S.J.C.M.M., Pluijm, S.M.F., van Dulmen-den Broeder, E., van Dorp, W., Laven, J.S.E.

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The influence of genetic variation on late toxicities in childhood cancer survivors: A review von Clemens, E., van der Kooi, A.L.F., Broer, L., van Dulmen-den Broeder, E., Visscher, H., Kremer, L., Tissing, W., Loonen, J., Ronckers, C.M., Pluijm, S.M.F., Neggers, S.J.C.M.M., Zolk, O., Langer, T., Zehnhoff-Dinnesen, A. am, Wilson, C.L., Hudson, M.M., Carleton, B., Laven, J.S.E., Uitterlinden, A.G., van den Heuvel-Eibrink, M.M.

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Diagnostic value of additional histopathological fascia examination in idiopathic inflammatory myopathies von Lim, J., Eftimov, F., Raaphorst, J., Aronica, E., Kooi, A. J.

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Randomized trial of intravenous immunoglobulin maintenance treatment regimens in chronic inflammatory demyelinating polyradiculoneuropathy von Kuitwaard, K., Brusse, E., Jacobs, B. C., Vrancken, A. F. J. E., Eftimov, F., Notermans, N. C., Kooi, A. J., Fokkink, W. ‐J. R., Nieboer, D., Lingsma, H. F., Merkies, I. S. J., Doorn, P. A.

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The lethal phenotype of a homozygous nonsense mutation in the lamin A/C gene von VAN ENGELEN, B. G. M, MUCHIR, A, HUTCHISON, C. J, VAN DER KOOI, A. J, BONNE, G, LAMMENS, M

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Opportunities and methodological challenges in EEG and MEG resting state functional brain network research von van Diessen, E, Numan, T, van Dellen, E, van der Kooi, A.W, Boersma, M, Hofman, D, van Lutterveld, R, van Dijk, B.W, van Straaten, E.C.W, Hillebrand, A, Stam, C.J

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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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Response to: Diagnostic value of additional histopathological fascia examination in idiopathic inflammatory myopathies von Lim, J., Eftimov, F., Raaphorst, J., Aronica, E., Kooi, A. J.

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Lamin A/C mutations with lipodystrophy, cardiac abnormalities, and muscular dystrophy von VAN DER KOOI, A. J, BONNE, G, SCHWARTZ, K, BUSCH, H. F. M, DE VISSER, M, EYMARD, B, DUBOC, D, TALIM, B, VAN DER VALK, M, REISS, P, RICHARD, P, DEMAY, L, MERLINI, L

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Rhabdomyolysis: Review of the literature von Zutt, R, van der Kooi, A.J, Linthorst, G.E, Wanders, R.J.A, de Visser, M

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The epidemiology of the Lambert-Eaton myasthenic syndrome in the Netherlands von WIRTZ, P. W, VAN DIJK, J. G, WINTZEN, A. R, VERSCHUUREN, J. J, VAN DOORN, P. A, VAN ENGELEN, B. G. M, VAN DER KOOI, A. J, KUKS, J. B, TWIJNSTRA, A, DE VISSER, M, VISSER, L. H, WOKKE, J. H

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The Lambert–Eaton myasthenic syndrome 1988–2008: A clinical picture in 97 patients von Titulaer, M.J, Wirtz, P.W, Kuks, J.B.M, Schelhaas, H.J, van der Kooi, A.J, Faber, C.G, van der Pol, W.L, de Visser, M, Sillevis Smitt, P.A.E, Verschuuren, J.J.G.M

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