Distinguishing acute-onset CIDP from fluctuating Guillain-Barré syndrome: A prospective study von RUTS, L, DRENTHEN, J, JACOBS, B. C, VAN DOOM, P. A

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Diagnostic and Classification Criteria for the Guillain-Barré Syndrome von van der Meché, F.G.A., van Doorn, P.A., Meulstee, J., Jennekens, F.G.I.

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Rasch-built Overall Disability Scale (R-ODS) for immune-mediated peripheral neuropathies von VAN NES, S. I, VANHOUTTE, E. K, VAN DOORN, P. A, HERMANS, M, BAKKERS, M, KUITWAARD, K, FABER, C. G, MERKIES, I. S. J

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Fatigue in immune-mediated polyneuropathies von MERKIES, I. S. J, SCHMITZ, P. I. M, SAMIJN, J. P. A, VAN DER MECHE, F. G. A, VAN DOORN, P. A

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Early recognition of poor prognosis in Guillain-Barré syndrome von WALGAARD, C, LINGSMA, H. F, RUTS, L, VAN DOORN, P. A, STEYERBERG, E. W, JACOBS, B. C

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OC07: Monitoring disease progression with electrophysiological markers derived from compound muscle action potential scans in amyotrophic lateral sclerosis von Sleutjes, B.T.H.M., Jacobsen, A.B., Tankisi, H., Sirin, N.G., Oge, A.E., Henderson, R.D., Van Doorn, P.A., Van Den Berg, L.H., Van Eijk, R.P.A.

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Prognostic factors of Guillain-Barré syndrome after intravenous immunoglobulin or plasma exchange von VISSER, L. H, SCHMITZ, P. I. M, MEULSTEE, J, VAN DOORN, P. A, VAN DER MECHE, F. G. A

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The Dutch neuromuscular database CRAMP (Computer Registry of All Myopathies and Polyneuropathies): Development and preliminary data von van Engelen, B.G.M, van Veenendaal, H, van Doorn, P.A, Faber, C.G, van der Hoeven, J.H, Janssen, N.G, Notermans, N.C, van Schaik, I.N, Visser, L.H, Verschuuren, J.J.G.M

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CMAP scan discontinuities: Automated detection and relation to motor unit loss von Sleutjes, B.T.H.M, Montfoort, I, Maathuis, E.M, Drenthen, J, van Doorn, P.A, Visser, G.H, Blok, J.H

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The Rasch-built Pompe-specific Activity (R-PAct) scale von van der Beek, N.A.M.E, Hagemans, M.L.C, van der Ploeg, A.T, van Doorn, P.A, Merkies, I.S.J

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Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease von Van der Beek, N.A.M.E, Hagemans, M.L.C, Reuser, A.J.J, Hop, W.C.J, Van der Ploeg, A.T, Van Doorn, P.A, Wokke, J.H.J

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Eight years experience with enzyme replacement therapy in two children and one adult with Pompe disease von van Capelle, C.I, Winkel, L.P.F, Hagemans, M.L.C, Shapira, S.K, Arts, W.F.M, van Doorn, P.A, Hop, W.C.J, Reuser, A.J.J, van der Ploeg, A.T

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G.P.11.10 Frequent pulmonary dysfunction in patients with late-onset Pompe disease necessitates careful evaluation during routine follow-up von van der Beek, N.A.M, van Capelle, C.I, van der Velden, K, Hop, W.C.J, Stam, H, van der Ploeg, A.T, van Doorn, P.A

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P2.47 Anoctamin 5 mutations in the Dutch limb girdle muscular dystrophy population von Frankhuizen, W.S, Verschuuren, J.J.G, van Doorn, P.A, de Visser, M, Ginjaar, H.B, van der Kooi, A.J

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Mild forms of Guillain-Barré syndrome in an epidemiologic survey in the Netherlands von VAN KONINGSVELD, R, VAN DOORN, P. A, SCHMITZ, P. I. M, ANG, C. W, VAN DER MECHE, F. G. A

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G.P.129 von Wens, S.C, Ciet, P, Perez-Rovira, A, Logie, K, Salamon, E, Wielopolski, P, Bruijne, M, Kruijshaar, M.E, Tiddens, H.W, van der Beek, N.A.M, van Doorn, P.A, van der Ploeg, A.T

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T.P.19 von de Vries, J.M, Kuperus, E, Hoogeveen-Westerveld, M, Wens, S.C.A, Kroos, M.A, Kruijshaar, M.E, van Doorn, P.A, van der Ploeg, A.T, Pijnappel, W.W.M

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Complete remission of skin lesions in a patient with subcorneal pustular dermatosis (Sneddon–Wilkinson disease) treated with antimyeloma therapy: association with disappearance of... von Borne, P.A., Jonkman, M.F., Doorn, R.

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Cardiac evaluation in children and adults with Pompe disease sharing the common c.−32-13T>G genotype rarely reveals abnormalities von van der Beek, N.A.M.E, Soliman, O.I.I, van Capelle, C.I, Geleijnse, M.L, Vletter, W.B, Kroos, M.A, Reuser, A.J.J, Frohn-Mulder, I.M.E, van Doorn, P.A, van der Ploeg, A.T

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IVIg treatment improves multifocal motor neuropathy: easy to start but difficult to stop von van Doorn, P A, van der Meché, F G

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