Comparing clinical data and muscle imaging of DYSF and ANO5 related muscular dystrophies von ten Dam, Leroy, van der Kooi, Anneke J, Rövekamp, Fleur, Linssen, Wim H.J.P, de Visser, Marianne

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Recessive Mutations in the Putative Calcium-Activated Chloride Channel Anoctamin 5 Cause Proximal LGMD2L and Distal MMD3 Muscular Dystrophies von Bolduc, Véronique, Marlow, Gareth, Boycott, Kym M., Saleki, Khalil, Inoue, Hiroshi, Kroon, Johan, Itakura, Mitsuo, Robitaille, Yves, Parent, Lucie, Baas, Frank, Mizuta, Kuniko, Kamata, Nobuyuki, Richard, Isabelle, Linssen, Wim H.J.P., Mahjneh, Ibrahim, de Visser, Marianne, Bashir, Rumaisa, Brais, Bernard

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Autosomal recessive limb‐girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients von ten Dam, Leroy, Frankhuizen, Wendy S., Linssen, Wim H.J.P., Straathof, Chiara S., Niks, Erik H., Faber, Karin, Fock, Annemarie, Kuks, Jan B., Brusse, Esther, de Coo, René, Voermans, Nicol, Verrips, Aad, Hoogendijk, Jessica E., van der Pol, Ludo, Westra, Dineke, de Visser, Marianne, van der Kooi, Anneke J., Ginjaar, Ieke

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Paroxysmal kinesigenic dyskinesia: Cortical or non-cortical origin von van Strien, Teun W, van Rootselaar, Anne-Fleur, Hilgevoord, Anthony A.J, Linssen, Wim H.J.P, Groffen, Alexander J.A, Tijssen, Marina A.J

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Tumefactive multiple sclerosis lesions under fingolimod treatment von Visser, Femke, Wattjes, Mike P, Pouwels, Petra J W, Linssen, Wim H J P, van Oosten, Bob W

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The ALS-FTD-Q: A new screening tool for behavioral disturbances in ALS von Raaphorst, Joost, Beeldman, Emma, Schmand, Ben, Berkhout, Joris, Linssen, Wim H.J.P., van den Berg, Leonard H., Pijnenburg, Yolande A., Grupstra, Hepke F., Weikamp, Janneke G., Schelhaas, H. Jurgen, Papma, Janne M., van Swieten, John C., de Visser, Marianne, de Haan, Rob J.

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Sumatriptan nasal spray in the acute treatment of migraine in adolescents and children von Callenbach, Petra M.C, Pels, Lise P.M, Mulder, Paul G.H, Linssen, Wim H.J.P, Gooskens, Rob H.J.M, van der Zwan, Jan L, Brouwer, Oebele F

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Cognitive dysfunction in lower motor neuron disease: executive and memory deficits in progressive muscular atrophy von Raaphorst, Joost, de Visser, Marianne, van Tol, Marie-José, Linssen, Wim H J P, van der Kooi, Anneke J, de Haan, Rob J, van den Berg, Leonard H, Schmand, Ben

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Neuromuscular findings in thyroid dysfunction: a prospective clinical and electrodiagnostic study von Duyff, Ruurd F, Van den Bosch, Joan, Laman, D Martin, van Loon, Bert-Jan Potter, Linssen, Wim H J P

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Benign prognosis in idiopathic hyper-CK-emia von Reijneveld, Jaap C., Notermans, Nicolette C., Linssen, Wim H.J.P., Wokke, John H.J.

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Benign prognosis in idiopathic hyper‐CK‐emia von Reijneveld, Jaap C., Notermans, Nicolette C., Linssen, Wim H.J.P., Wokke, John H.J.

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Variability and interrelationships of surface EMG parameters during local muscle fatigue von Linssen, Wim H. J. P., Stegeman, Dick F., Joosten, Ed M. G., Notermans, Servaas L. H., van't Hof, Martin A., Binkhorst, Rob A.

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Reduced sensory anticipation in migraine von MULDER, ELLES J.C.M., LINSSEN, WIM H.J.P., DE GEUS, ECO J.C.

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Fatigue in type I fiber predominance: A muscle force and surface EMG study on the relative role of type I and type II muscle fibers von Linssen, Wim H. J. P., Stegeman, Dick F., Joosten, Ed M. G., Binkhorst, Rob A., Merks, Mieke J. H., Laak, Henk J. Ter, Notermans, Servaas L. H.

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Muscle fiber action potential changes and surface EMG: A simulation study von Stegeman, Dick F., Linssen, Wim H.J.P.

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A behavioral treatment of young migrainous and nonmigrainous headache patients: prediction of treatment success von Osterhaus, S O, Lange, A, Linssen, W H, Passchier, J

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Isolated Intramedullary Tuberculosis Presenting as a Conus Tumor von Sie, Lilian T. L., Linssen, Wim H. J. P.

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Electromyographic evidence of delayed fatigue-induced sarcolemmal excitability impairment in McArdle's disease von Linssen, Wim H.J.P., Stegeman, Dick F., Merks, Mieke J.H., Binkhorst, Rob A., Notermans, Servaas L.H.

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Vascular insufficiency of the cervical cord due to hyperextension of the spine von Linssen, Wim H.J.P., Praamstra, Peter, Gabreëls, Fons J.M., Rotteveel, Jan J.

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Deafness, sensory neuropathy, and ovarian dysgenesis: A new syndrome or a broader spectrum of Perrault syndrome? von Linssen, Wim H. J. P., Van den Bent, Martin J., Brunner, Han G., Poels, Petra J. E.

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