P3 Development of anoctaminopathy immunodiagnostics using the novel ANO5–5F7 antibody by Bashir, R, Ramachandran, U, Rabelo, B, Exton, J, Henderson, M, Dubuisson, A, Kiuru-Enari, S, de Visser, M, Linssen, W.H.J.P, Baas, F, Mahjneh, I, Barresi, R

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Is cardiovascular disease a risk factor in the development of axonal polyneuropathy? by Teunissen, L L, Franssen, H, Wokke, J H J, van der Graaf, Y, Linssen, W H J P, Banga, J D, Laman, D M, Notermans, N C

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Interictal and Postictal Contingent Negative Variation in Migraine Without Aura by Mulder, E.J.C.M., Linssen, W.H.J.P., Passchier, J., De Geus, E.J.C.

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Genetic heterogeneity in Miyoshi-type distal muscular dystrophy by Linssen, W.H.J.P, de Visser, M, Notermans, N.C, Vreyling, J.P, Van Doorn, P.A, Wokke, J.H.J, Baas, F, Bolhuis, P.A

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Hyper-CK-aemia revisited by Reijneveld, J.C., Notermans, N.C., Linssen, W.H.J.P., Bär, P.R., Wokke, J.H.J.

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Bilateral foot drop as the first symptom of nemaline myopathy by Hoeksema, D.G., Linssen, W.H.J.P., Smit, L.M.E.

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Effects of Medication Use on Health State in Postictal Migraineurs by Mulder, E.J.C.M., Passchier, J., Linssen, W.H.J.P., De Geus, E.J.C.

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Two sisters with autosomal recessive limb-girdle muscular dystrophy with gamma-sarcoglycanopathy (LGMD2C) by Broere, D., Linssen, W.H.J.P., Smit, L.M.E., Ginjaar, H.B.

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Two sisters with sever childhood recessive muscular dystrophy (SCARMD) with a γ-sarcoglycanopathy maped on chromosome 13q12 by Broere, D., Linssen, W.H.J.P., Ginjaar, H.B., Smit, L.M.E.

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Progressive swelling and stiffness of the extremities: another case of eosinophilic fasciitis by Broere, D., vd Bosch, J., Hellemans, H.P.R., Vasmel, W.L.E., Linssen, W.H.J.P.

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Miyoshi-type distal muscular dystrophy: clinical features of 24 Dutch patients by Linssen, W.H.J.P., De Visser, M., Notermans, N.C., Wokke, J.H.J., Van Doorn, P.A., Höweler, C.J., De Jager, A.E.J.

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