Arteriovenous Fistula Maturation Failure in a Large Cohort of Hemodialysis Patients in the Netherlands von Voorzaat, Bram M., van der Bogt, Koen E. A., Janmaat, Cynthia J., van Schaik, Jan, Dekker, Friedo W., Rotmans, Joris I.

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Botulinum toxin effect on salivary flow rate in children with cerebral palsy von JONGERIUS, P. H, ROTTEVEEL, J. J, VAN LIMBEEK, J, GABREËLS, F. J. M, VAN HULST, K, VAN DEN HOOGEN, F. J. A

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Complex regional pain syndrome type I (RSD): Pathology of skeletal muscle and peripheral nerve von VAN DER LAAN, L, TER LAAK, H. J, GABREËLS-FESTEN, A, GABREËLS, F, GORIS, R. J. A

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A new leukoencephalopathy with vanishing white matter von VAN DER KNAAP, M. S, BARTH, P. G, GABREËLS, F. J. M, FRANZONI, E, BEGEER, J. H, STROINK, H, ROTTEVEEL, J. J, VALK, J

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Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis von Verrips, Aad, Hoefsloot, Lies H., Steenbergen, Gerry C. H., Theelen, Joop P., Wevers, Ron A., Gabreëls, Fons J. M., van Engelen, Baziel G. M., van den Heuvel, Lambert P. W. J.

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Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease von GABREËLS-FESTEN, A. A. W. M, HOOGENDIJK, J. E, VAN ENGELEN, B. G. M, VAN BROECKHOVEN, C, MARIMAN, E. C. M, MEIJERINK, P. H. S, GABREËLS, F. J. M, BOLHUIS, P. A, VAN BEERSUM, S, KULKENS, T, NELIS, E, JENNEKENS, F. G. I, DE VISSER, M

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L-dopa-responsive infantile hypokinetic rigid parkinsonism due to tyrosine hydroxylase deficiency von DE RIJK-VAN ANDEL, J. F, GABREËLS, F. J. M, GEURTZ, B, STEENBERGEN-SPANJERS, G. C. H, VAN DEN HEUVEL, L. P. W. J, SMEITINK, J. A. M, WEVERS, R. A

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Improvement of radiocephalic fistula maturation: rationale and design of the Liposomal Prednisolone to Improve Hemodialysis Fistula Maturation (LIPMAT) study – a randomized control... von Voorzaat, Bram M., van Schaik, Jan, van der Bogt, Koen E.A., Vogt, Liffert, Huisman, Laurens, Gabreëls, Bas A. Th. F., van der Meer, Irene M., van Eps, Randolph G.S., Eefting, Daniël, Weijmer, Marcel C., Groeneveld, Han O., van Nieuwenhuizen, Roos C., Boom, Henk, Verburgh, Cornelis A., van der Putten, Karien, Rotmans, Joris I.

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The prevalence of mental retardation: a critical review of recent literature von Roeleveld, Nel, Zielhuis, Gerhard A.

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Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis von Verrips, A., Lycklama à Nijeholt, G. J., Barkhof, F., Van Engelen, B. G. M., Wesseling, P., Luyten, J. A. F. M., Wevers, R. A., Stam, J., Wokke, J. H. J., van den Heuvel, L. P. W. J., Keyser, A., Gabreëls, F. J. M.

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Hereditary neuropathy with liability to pressure palsies : Phenotypic differences between patients with the common deletion and a pmp22 frame shift mutation von LENSSEN, P. P. A, GABREËLS-FESTEN, A. A. W. M, VALENTIJN, L. J, JONGEN, P. J. H, VAN BEERSUM, S. E. C, VAN ENGELEN, B. G. M, VAN WENSEN, P. J. M, BOLHUIS, P. A, GABREËLS, F. J. M, MARIMAN, E. C. M

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Rhabdomyolysis: a review of the literature von Poels, P.J.E., Gabreëls, F.J.M.

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A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome von de Vries, D. Daniëlle, van Engelen, Baziel G. M., Gabreëls, Fons J. M., Ruitenbeek, Wim, van Oost, Bernard A.

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A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects? von van der Put, Nathalie M.J., Gabreëls, Fons, Stevens, Erik M.B., Smeitink, Jan A.M., Trijbels, Frans J.M., Eskes, Tom K.A.B., van den Heuvel, Lambert P., Blom, Henk J.

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MECP2 Mutation in a Boy with Severe Neonatal Encephalopathy: Clinical, Neuropathological and Molecular Findings von Geerdink, N., Rotteveel, J. J., Lammens, M., Sistermans, E. A., Heikens, G. T., Gabreëls, F. J. M., Mullaart, R. A., Hamel, B. C. J.

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Biochemical hallmarks of tyrosine hydroxylase deficiency von Brautigam, Christa, Wevers, Ron A, Jansen, Riet J. T, Smeitink, Jan A. M, Andel, Johanneke F. de Rijk-van, Gabreels, Fons J. M, Hoffmann, Georg F

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Charcot-Marie-Tooth disease type 1A : morphological phenotype of the 17p duplication versus PMP22 point mutations von GABREËLS-FESTEN, A. A. W. M, BOLHUIS, P. A, HOOGENDIJK, J. E, VALENTIJN, L. J, ESHUIS, E. J. H. M, GABREËLS, F. J. M

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Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia von HIEL, J. A. P, VAN ENGELEN, B. G. M, LAST, J. I, TAYLOR, A. M. R, WEEMAES, C. M. R, BROEKS, A, VERRIPS, A, TER LAAK, H, VINGERHOETS, H. M, VAN DEN HEUVEL, L. P. W, LAMMENS, M, GABREËLS, F. J. M

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A Randomized Trial of Liposomal Prednisolone (LIPMAT) to Enhance Radiocephalic Fistula Maturation: A Pilot Study von Voorzaat, Bram M., van der Bogt, K.E.A., Bezhaeva, Taisiya, van Schaik, Jan, Eefting, Daniel, van der Putten, Karien, van Nieuwenhuizen, Roos C., Groeneveld, Johannes O., Hoogeveen, Ellen K., van der Meer, Irene M., Statius van Eps, Randolph G., Vogt, Liffert, Huisman, Laurens, Gabreëls, Bas A.Th.F., Boom, Henk, Verburgh, Cornelis A., Boon, Diederik, Metselaar, Josbert M., Weijmer, Marcel C., Rotmans, Joris I.

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Histology of hereditary neuralgic amyotrophy von van Alfen, N, Gabreëls-Festen, A A W M, ter Laak, H J, Arts, W F M, Gabreëls, F J M, van Engelen, B G M

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