Autism and behavior in adult patients with Dravet syndrome (DS) von Berkvens, J.J.L, Veugen, I, Veendrick-Meekes, M.J.B.M, Snoeijen-Schouwenaars, F.M, Schelhaas, H.J, Willemsen, M.H, Tan, I.Y, Aldenkamp, A.P

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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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Paroxysmal sensory (spinal) attacks without hyperexplexia in a patient with a variant in the GLRA1 gene von Zwarts, M.J, Willemsen, M.H, Kamsteeg, E.-J, Schelhaas, H.J

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P 248. Cortical inhibition by Retigabine in epilepsy patients: Assessment by transcranial magnetic stimulation von Munneke, M.A.M, Zwarts, M.J, Stegeman, D.F, Schelhaas, H.J, Kleine, B.U

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Carbamazepine and oxcarbazepine in adult patients with Dravet syndrome: Friend or foe? von Snoeijen-Schouwenaars, F.M, Veendrick, M.J.B.M, van Mierlo, P, van Erp, G, de Louw, A.J.A, Kleine, B.U, Schelhaas, H.J, Tan, I.Y

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W11.3 Cortical modulation in patients with amyotrophic lateral sclerosis von Munneke, M.A.M, Zwarts, M.J, Rongen, J.J, Schelhaas, H.J, Stegeman, D.F

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S35-5 Mechanisms of fasciculation von Kleine, B.U, Stegeman, D.F, Schelhaas, H.J, Zwarts, M.J

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Inhibition of cortical excitability by retigabine: Measurement of intracortical inhibition using transcranial magnetic stimulation von Zwarts, M.J, Munneke, M.A.M, Stegeman, D.F, Schelhaas, H.J, Kleine, B.U

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Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation von Overeem, S, Schelhaas, H.J, Blijham, P.J, Grootscholten, M.I, ter Laak, H.J, Timmermans, J, van den Wijngaard, A, Zwarts, M.J

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C.P.3 Genetic and clinical heterogeneity of RYR1-related myopathies in a cohort of 60 Dutch families with identification of 40 novel mutations von Voermans, N.C, Jungbluth, H, Raaphorst, J, Snoeck, M, Straathof, C, Schelhaas, H.J, Sie, L, de Coo, R, van de Pol, W, de Visser, M, Scheffer, H, Kamsteeg, E.J, van Engelen, B.G.M

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Electrodiagnostic criteria for ALS: Time to STARD von Schelhaas, H.J, Kleine, B.U, Zwarts, M.J

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P12-20 Age-related changes in motor unit number estimates in adult patients with Charcot-Marie-Tooth type 1A von van Dijk, J.P, Verhamme, C, van Schaik, I.N, Schelhaas, H.J, Mans, E, Bour, L.J, Stegeman, D.F, Zwarts, M.J

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Family history of neurodegenerative and vascular diseases in ALS: A population-based study von HUISMAN, M. H. B, DE JONG, S. W, VERWIJS, M. C, SCHELHAAS, H. J, VAN DER KOOI, A. J, DE VISSER, M, VELDINK, J. H, VAN DEN BERG, L. H

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Transient cerebral white matter lesions in a patient with connexin 32 missense mutation von SCHELHAAS, H. J, VAN ENGELEN, B. G. M, GABREËLS-FESTEN, A. A. W. M, HAGEMAN, G, VLIEGEN, J. H. R, VAN DER KNAAP, M. S, ZWARTS, M. J

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Demyelinating polyneuropathy in Leber hereditary optic neuropathy von Gilhuis, H.J., Schelhaas, H.J., Cruysberg, J.R.M., Zwarts, M.J.

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Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia von SCHELHAAS, H. J, IPPEL, P. F, HAGEMAN, G, SINKE, R. J, VAN DER LAAN, E. N, BEEMER, F. A

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N.P.1 04 Neuropathy in degenerative early-onset cerebellar ataxias von Bos, M.M., Schelhaas, H.J., van de Warrenburg, B.P.C., Zwarts, M.J., Kremer, H.P.H.

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Cerebellar ataxia, dementia, pyramidal signs, cortical cataract of the posterior pole and a raised IgG index in a patient with a sporadic form of olivopontocerebellar atrophy von Schelhaas, H.J., Hageman, G., Post, J.G.

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Early onset cerebellar ataxia with retained tendon reflexes: foot deformity in a first grade family member von Schelhaas, H.J, Hulst, M.v.d, Ippel, E, Prevo, R.L, Hageman, G

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MRI locates a posterior fossa aneurysm in the fourth ventricle von Schelhaas, H.J, Brouwers, P.J.A.M, van der AA, H.E, Prevo, R.L

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