Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients von Saris, Christiaan G J, Horvath, Steve, van Vught, Paul W J, van Es, Michael A, Blauw, Hylke M, Fuller, Tova F, Langfelder, Peter, DeYoung, Joseph, Wokke, John H J, Veldink, Jan H, van den Berg, Leonard H, Ophoff, Roel A

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Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis von Ophoff, Roel A, van den Berg, Leonard H, van Es, Michael A, van Vught, Paul WJ, Blauw, Hylke M, Franke, Lude, Saris, Christiaan GJ, Van Den Bosch, Ludo, de Jong, Sonja W, de Jong, Vianney, Baas, Frank, van't Slot, Ruben, Lemmens, Robin, Schelhaas, Helenius J, Birve, Anna, Sleegers, Kristel, Van Broeckhoven, Christine, Schymick, Jennifer C, Traynor, Bryan J, Wokke, John HJ, Wijmenga, Cisca, Robberecht, Wim, Andersen, Peter M, Veldink, Jan H

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Magnesium treatment for patients with refractory status epilepticus due to POLG1-mutations von Visser, Nora A., Braun, Kees P. J., Leijten, Frans S. S., van Nieuwenhuizen, Onno, Wokke, John H. J., van den Bergh, Walter M.

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Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis von Piepers, Sanne, Veldink, Jan H., De Jong, Sonja W., Van Der Tweel, Ingeborg, Van Der Pol, W-Ludo, Uijtendaal, Esther V., Schelhaas, H. Jurgen, Scheffer, Hans, De Visser, Marianne, De Jong, J. M. B. Vianney, Wokke, John H. J., Groeneveld, Geert Jan, Van Den Berg, Leonard H.

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Clinical features of late-onset Pompe disease: A prospective cohort study von Wokke, John H.J., Escolar, Diana M., Pestronk, Alan, Jaffe, Kenneth M., Carter, Gregory T., van den Berg, Leonard H., Florence, Julaine M., Mayhew, Jill, Skrinar, Alison, Corzo, Deyanira, Laforet, Pascal

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Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study von Dierick, Ines, Baets, Jonathan, Irobi, Joy, Jacobs, An, De Vriendt, Els, Deconinck, Tine, Merlini, Luciano, Van den Bergh, Peter, Rasic, Vedrana Milic, Robberecht, Wim, Fischer, Dirk, Morales, Raul Juntas, Mitrovic, Zoran, Seeman, Pavel, Mazanec, Radim, Kochanski, Andrzej, Jordanova, Albena, Auer-Grumbach, Michaela, Helderman-van den Enden, A. T. J. M., Wokke, John H. J., Nelis, Eva, De Jonghe, Peter, Timmerman, Vincent

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Cold paresis in multifocal motor neuropathy von Straver, Dirk C. G., van Asseldonk, Jan-Thies H., Notermans, Nicolette C., Wokke, John H. J., van den Berg, Leonard H., Franssen, Hessel

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A randomized sequential trial of creatine in amyotrophic lateral sclerosis von Jan Groeneveld, Geert, Veldink, Jan H., van der Tweel, Ingeborg, Kalmijn, Sandra, Beijer, Cornelis, de Visser, Marianne, Wokke, John H. J., Franssen, Hessel, Berg, Leonard H. van den

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Pre‐ and postsynaptic neuromuscular junction abnormalities in musk myasthenia von Niks, Erik H., Kuks, Jan B.M., Wokke, John H.J., Veldman, Henk, Bakker, Egbert, Verschuuren, Jan J.G.M., Plomp, Jaap J.

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Recombinant human insulin‐like growth factor I (rhIGF‐I) for the treatment of amyotrophic lateral sclerosis/motor neuron disease von Beauverd, Michel, Mitchell, J D, Wokke, John HJ, Borasio, Gian Domenico, Beauverd, Michel

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Another milestone in childhood spinal muscular atrophy von Wokke, John H

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Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen von Blauw, Hylke M, MD, Veldink, Jan H, PhD, van Es, Michael A, MD, van Vught, Paul W, PhD, Saris, Christiaan GJ, MD, van der Zwaag, Bert, PhD, Franke, Lude, MSc, Burbach, J Peter H, PhD, Wokke, John H, MD, Ophoff, Roel A, PhD, van den Berg, Leonard H, MD

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Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study von van der Beek, Nadine A M E, de Vries, Juna M, Hagemans, Marloes L C, Hop, Wim C J, Kroos, Marian A, Wokke, John H J, de Visser, Marianne, van Engelen, Baziel G M, Kuks, Jan B M, van der Kooi, Anneke J, Notermans, Nicolette C, Faber, Karin G, Verschuuren, Jan J G M, Reuser, Arnold J J, van der Ploeg, Ans T, van Doorn, Pieter A

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Quantification of SMN protein in leucocytes from spinal muscular atrophy patients: effects of treatment with valproic acid von Piepers, Sanne, Cobben, Jan-Maarten, Sodaar, Peter, Jansen, Marc D, Wadman, Renske I, Meester-Delver, Ann, Poll-The, Bwee Tien, Lemmink, Henny H, Wokke, John H J, van der Pol, W-Ludo, van den Berg, Leonard H

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Increased expression of rapsyn in muscles prevents acetylcholine receptor loss in experimental autoimmune myasthenia gravis von Losen, Mario, Stassen, Maurice H. W., Martínez-Martínez, Pilar, Machiels, Barbie M., Duimel, Hans, Frederik, Peter, Veldman, Henk, Wokke, John H. J., Spaans, Frank, Vincent, Angela, De Baets, Marc H.

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Drug treatment for spinal muscular atrophy types II and III von Wadman, Renske I, Bosboom, Wendy M J, van der Pol, W Ludo, van den Berg, Leonard H, Wokke, John H J, Iannaccone, Susan T, Vrancken, Alexander F J E

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Entrapment in anti myelin-associated glycoprotein neuropathy von Faber, Catharina G., Notermans, Nicolette C., Wokke, John H. J., Franssen, Hessel

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Spastin mutations in sporadic adult-onset upper motor neuron syndromes von Brugman, Frans, Wokke, John H. J., Scheffer, Hans, Versteeg, Martina H. A., Sistermans, Erik A., van den Berg, Leonard H.

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Genome-wide association study identifies 19p13.3 ( UNC13A ) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis von Giegling, Ina, Lemmens, Robin, Kiemeney, Lambertus A, Ophoff, Roel A, Zwarts, Machiel J, Hofman, Albert, Hendrich, Corinna, Landers, John E, Saris, Christiaan G J, Veldink, Jan H, Melki, Judith, Fumoto, Katsumi, Andersen, Peter M, Birve, Anna, Schreiber, Stefan, de Visser, Marianne, Hardiman, Orla, Uitterlinden, Andre G, Nöthen, Markus M, Meininger, Vincent, Waibel, Stefan, Cichon, Sven, Leigh, P Nigel, Wichmann, H-Erich, Ludolph, Albert C, van Es, Michael A, Vermeulen, Sita H H M, Robberecht, Wim, Meyer, Thomas, Schelhaas, Helenius J, van Vught, Paul W J, Groen, Ewout J N, Rivadeneira, Fernando, Purcell, Shaun, Cronin, Simon, Estrada, Karol, van den Berg, Leonard H, Glass, Jonathan D, Huisman, Mark H B, Slowik, Agnieszka, Wokke, John H J, Pasterkamp, R Jeroen, Brown, Robert H, Shaw, Christopher E, van der Kooi, Anneke J, Tomik, Barbara, van Doormaal, Perry T C, Rujescu, Dan, McLaughlin, Russell L, Dahlberg, Caroline, Al-Chalabi, Ammar, Blauw, Hylke M, Strengman, Eric, Muglia, Pierandrea

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ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study von van Es, Michael A, MD, Van Vught, Paul W, MSc, Blauw, Hylke M, MD, Franke, Lude, MSc, Saris, Christiaan G, MD, Andersen, Peter M, MD, Van Den Bosch, Ludo, PhD, de Jong, Sonja W, MD, van 't Slot, Ruben, BSc, Birve, Anna, PhD, Lemmens, Robin, MD, de Jong, Vianney, MD, Baas, Frank, PhD, Schelhaas, Helenius J, MD, Sleegers, Kristel, MD, Van Broeckhoven, Christine, PhD, Wokke, John HJ, MD, Wijmenga, Cisca, PhD, Robberecht, Wim, MD, Veldink, Jan H, MD, Ophoff, Roel A, PhD, van den Berg, Leonard H, MD

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