DENOVO MUTATION IN HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-1 von HOOGENDIJK, JE, HENSELS, GW, GABREELSFESTEN, AAWM, GABREELS, FJM, JANSSEN, EAM, DEJONGHE, P, MARTIN, JJ, VAN BROECKHOVEN, C, VALENTIJN, LJ, BAAS, F, DEVISSER, M, BOLHUIS, PA

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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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Schwann cell differentiation in Charcot-Marie-Tooth disease type 1A (CMT1A) : normal number of myelinating Schwann cells in young CMT1A patients and neural cell adhesion molecule e... von HANEMANN, C. O, GABREËLS-FESTEN, A. A. W. M, STOLL, G, MÜLLER, H. W

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Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsies von Mariman, E. C. M., Gabreëls-Festen, A. A. W. M., van Beersum, S. E. C., Valentijn, L. J., Baas, F., Bolhuis, P. A., Jongen, P. J. H., Ropers, H. H., Gabreëls, F. J. M.

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Hereditary neuropathy with liability to pressure palsies: A clinical, electroneurophysiological and morphological study von Verhagen, W.I.M., Gabreëls-Festen, A.A.W.M., van Wensen, P.J.M., Joosten, E.M.G., Vingerhoets, H.M., Gabreëls, F.J.M., de Graaf, R.

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Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy : A clinical and electrophysiological study von TEUNISSEN, L. L, NOTERMANS, N. C, WOKKE, J. H. J, FRANSSEN, H, VAN DER GRAAF, Y, OEY, P. L, LINSSEN, W. H. J. P, VAN ENGELEN, B. G. M, IPPEL, P. F, VAN DIJK, G. W, GABREELS-FESTEN, A. A. W. M

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Low affinity NGF receptor expression in CMT1A nerve biopsies of different disease stages von HANEMANN, C. O, GABREËLS-FESTEN, A. A. W. M, MÜLLER, H. W, STOLL, G

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Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status von Domburg, P. H. M. F. van, Gabreëls-Festen, A. A. W. M., Gabreëls, F. J. M., Coo, R. de, Ruitenbeek, W., Wesseling, P., Laak, H. ter

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Clinically distinct codon 69 mutations in major myelin protein zero in demyelinating neuropathies von Meijerink, Peter H. S., Zorn, Ina, Baas, Frank, de Visser, Marianne, Bolhuis, Pieter A., Hoogendijk, Jessica E., Veldman, Henk, Gabreëls-Festen, Anneke A. W. M.

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Early morphological features in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I) von Gabreëls-Festen, A.A.W.M., Joosten, E.M.G., Gabreëls, F.J.M., Jennekens, F.G.I., Kempen, T.W.Janssen-van

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HEREDITARY MOTOR AND SENSORY NEUROPATHY OF NEURONAL TYPE WITH ONSET IN EARLY CHILDHOOD von GABREËLS-FESTEN, A. A. W. M., JOOSTEN, E. M. G., GABREËLS, F. J. M., JENNEKENS, F. G. I., GOOSKENS, R. H. J. M., STEGEMAN, D. F.

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Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies von MARIMAN, E. C. M, GABREËLS-FESTEN, A. A. W. M, VAN BEERSUM, S. E. C, JONGEN, P. J. H, VAN DE LOOIJ, E, BAAS, F, BOLHUIS, P. A, ROPERS, H. H, GABREËLS, F. J. M

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CONGENITAL DEMYELINATING MOTOR AND SENSORY NEUROPATHY WITH FOCALLY FOLDED MYELIN SHEATHS von GABREËLS-FESTEN, A. A. W. M., JOOSTEN, E. M. G., GABREËLS, F. J. M., STEGEMAN, D. F., VOS, A. J. M., BUSCH, H. F. M.

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The status of HMSN type III von Gabreëls-Festen, A.A.W.M., Gabreëls, F.J.M., Jennekens, F.G.I., Janssen-van Kempen, T.W.

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Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy ? Diagnostic value of morphological criteria von GABREËLS-FESTEN, A. A. W. M, GABREËLS, F. J. M, HOOGENDIJK, J. E, BOLHUIS, P. A, JONGEN, P. J. H, VINGERHOETS, H. M

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Conduction velocity distributions compared to fiber size distributions in normal human sural nerve von van Veen, Benno K., Schellens, Ronald L. L. A., Stegeman, Dick F., Schoonhoven, Ruurd, Gabreëls-Festen, Anneke A. W. M.

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Peripheral Nerve Elongation by Laser Doppler Flowmetry-Monitored Expansion: An Experimental Basis for Future Application in the Management of Peripheral Nerve Defects von van der Wey, Leo Peter, Polder, Theo W, Stegeman, Dick F, W. M. Gabreëls-Festen, Anneke A, Spauwen, Paul H. M, Gabreëls, Fons J. M

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Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1 von MARIMAN, E. C. M, GABREËLS-FESTEN, A. A. W. M, VAN BEERSUM, S. E. C, JONGEN, P. J. H, ROPERS, H.-H, GABREËLS, F. J. M

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Hereditary Neuropathy with Liability to Pressure Palsies in Childhood von Gabreëls-Festen, A. A. W. M., Gabreëls, F.J. M., Joosten, E. M. G., Vingerhoets, H. M., Renier, W. O.

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A statistical approach to fiber diameter distribution in human sural nerve von Schellens, Ronald L. L. A., van Veen, Benno K., Gabreëls-Festen, Annexe A. W. M., Notermans, Servaas L. H., van't Hof, Martin A., Stegeman, Dick F.

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