Building centres of expertise according to the Dutch model? von Gabreëls, Fons JM, Huizer, Jolanda S

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Validity and reproducibility of a new diagnostic motor performance test in children with suspected myopathy von van den Beld, Willeke A, van der Sanden, Gitty AC, Sengers, Rob CA, Verbeek, André LM, Gabreëls, Fons JM

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Regulation and expression of the murine PMP22 gene von van de Wetering, R A, Gabreëls-Festen, A A, Kremer, H, Kalscheuer, V M, Gabreëls, F J, Mariman, E C

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Neurodevelopment in offspring‐of hairdressers von Kersemaekers, Wendy M, Roeleveld, Nel, PhD, Gerhard AZielhuis, Gabreëls, Fons JM

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A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome von Tranebjaerg, L, Hamel, B C, Gabreels, F J, Renier, W O, Van Ghelue, M

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Neurophysiological studies in the Leigh syndrome von Van Erven, Paul MM, Colon, Ernst J, Gabreëls, Fons JM, Renier, Willy O, Vingerhoets, Dick M

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Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and a maternal uncle von Renier, Willy O, Gabreëls, Fons JM, Hustinx, Theo WJ, Thijssen, Henk OM, Ter Haar, Ben GA, Kroll, Els W, Beckers, Henk

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Muscle Reflexes and Synergies Triggered by an Unexpected Support Surface Height During Walking von van der Linden, Marleen H, Marigold, Daniel S, Gabreels, Fons J.M, Duysens, Jacques

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Increased Cerebrospinal Fluid Glycine: A Biochemical Marker for a Leukoencephalopathy With Vanishing White Matter von van der Knaap, Marjo S., Wevers, Ron A., Kure, Shigeo, Gabreëls, Fons J. M., Verhoeven, Nanda M., van Raaij-Selten, Bertie, Jaeken, Jaak

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