Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy von Neveling, Kornelia, Martinez-Carrera, Lilian A., Hölker, Irmgard, Heister, Angelien, Verrips, Aad, Hosseini-Barkooie, Seyyed Mohsen, Gilissen, Christian, Vermeer, Sascha, Pennings, Maartje, Meijer, Rowdy, te Riele, Margot, Frijns, Catharina J.M., Suchowersky, Oksana, MacLaren, Linda, Rudnik-Schöneborn, Sabine, Sinke, Richard J., Zerres, Klaus, Lowry, R. Brian, Lemmink, Henny H., Garbes, Lutz, Veltman, Joris A., Schelhaas, Helenius J., Scheffer, Hans, Wirth, Brunhilde

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People with epilepsy and intellectual disability: More than a sum of two conditions von Snoeijen-Schouwenaars, Francesca M., Young, Charlotte, Rowe, Charles, van Ool, Jans S., Schelhaas, Helenius J., Shankar, Rohit

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Autoantibodies to cytosolic 5′-nucleotidase 1A in inclusion body myositis von Pluk, Helma, van Hoeve, Bas J. A., van Dooren, Sander H. J., Stammen-Vogelzangs, Judith, van der Heijden, Annemarie, Schelhaas, Helenius J., Verbeek, Marcel M., Badrising, Umesh A., Arnardottir, Snjolaug, Gheorghe, Karina, Lundberg, Ingrid E., Boelens, Wilbert C., van Engelen, Baziel G., Pruijn, Ger J. M.

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Evidence for an oligogenic basis of amyotrophic lateral sclerosis von van Blitterswijk, Marka, van Es, Michael A, Hennekam, Eric A M, Dooijes, Dennis, van Rheenen, Wouter, Medic, Jelena, Bourque, Pierre R, Schelhaas, Helenius J, van der Kooi, Anneke J, de Visser, Marianne, de Bakker, Paul I W, Veldink, Jan H, van den Berg, Leonard H

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Postoperative urinary retention or difficulties to empty the bladder in young patients undergoing posterior spinal fusion for adolescent idiopathic scoliosis von Keskinen, Heli, Helenius, Linda, Pajulo, Olli, Helenius, Ilkka J.

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Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19 von Duarri, Anna, Jezierska, Justyna, Fokkens, Michiel, Meijer, Michel, Schelhaas, Helenius J., den Dunnen, Wilfred F. A., van Dijk, Freerk, Verschuuren-Bemelmans, Corien, Hageman, Gerard, van de Vlies, Pieter, Küsters, Benno, van de Warrenburg, Bart P., Kremer, Berry, Wijmenga, Cisca, Sinke, Richard J., Swertz, Morris A., Kampinga, Harm H., Boddeke, Erik, Verbeek, Dineke S.

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SCN1A-deficient excitatory neuronal networks display mutation-specific phenotypes von van Hugte, Eline J H, Lewerissa, Elly I, Wu, Ka Man, Scheefhals, Nicky, Parodi, Giulia, van Voorst, Torben W, Puvogel, Sofia, Kogo, Naoki, Keller, Jason M, Frega, Monica, Schubert, Dirk, Schelhaas, Helenius J, Verhoeven, Judith, Majoie, Marian, van Bokhoven, Hans, Nadif Kasri, Nael

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Psychogenic non‐epileptic (functional) seizures in adults with intellectual disability and epilepsy: A matched case–control study von Kloosterman, Iris E. M., Haenen, Alexandra I., Poortvliet‐Koedam, Esther L. G. E., Lazeron, Richard H. C., Schelhaas, Helenius J., Ool, Jans S.

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A systematic review of neuropsychiatric comorbidities in patients with both epilepsy and intellectual disability von van Ool, Jans S, Snoeijen-Schouwenaars, Francesca M, Schelhaas, Helenius J, Tan, In Y, Aldenkamp, Albert P, Hendriksen, Jos G.M

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A Rare Complication of Thoracic Spine Surgery: Pediatric Horner's Syndrome after Posterior Vertebral Column Resection-A Case Report von Grabala, Pawel, Danowska-Idziok, Kinga, Helenius, Ilkka J

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The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions von SIMON-SANCHEZ, Javier, DOPPER, Elise G. P, SMITS, Marion, RAAPHORST, Joost, DEN BERG, Leonard H. Van, SCHELHAAS, Helenius J, DE DIE-SMULDERS, Christine E. M, MAJOOR-KRAKAUER, Danielle, ROZEMULLER, Annemieke J. M, WILLEMSEN, Rob, PIJNENBURG, Yolande A. L, HEUTINK, Peter, COHN-HOKKE, Petra E, SWIETEN, John C. Van, HUKEMA, Renate K, NICOLAOU, Nayia, SEELAAR, Harro, DE GRAAF, J. Roos A, DE KONING, Inge, SCHOOR, Natasja M. Van, DEEG, Dorly J. H

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UNC13A is a modifier of survival in amyotrophic lateral sclerosis von Diekstra, Frank P, van Vught, Paul W.J, van Rheenen, Wouter, Koppers, Max, Pasterkamp, R. Jeroen, van Es, Michael A, Schelhaas, Helenius J, de Visser, Marianne, Robberecht, Wim, Van Damme, Philip, Andersen, Peter M, van den Berg, Leonard H, Veldink, Jan H

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Diagnostic exome sequencing in 100 consecutive patients with both epilepsy and intellectual disability von Snoeijen‐Schouwenaars, Francesca M., van Ool, Jans S., Verhoeven, Judith S., Mierlo, Petra, Braakman, Hilde M. H., Smeets, Eric E., Nicolai, Joost, Schoots, Jeroen, Teunissen, Mariel W. A., Rouhl, Rob P. W., Tan, In Y., Yntema, Helger G., Brunner, Han G., Pfundt, Rolph, Stegmann, Alexander P., Kamsteeg, Erik‐Jan, Schelhaas, Helenius J., Willemsen, Marjolein H.

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Outcomes of early hemivertebrectomy in children with congenital scoliosis: A prospective follow-up study von Oksanen, Hanna M., Jalanko, Tuomas, Helenius, Ilkka J.

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VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient von van Blitterswijk, Marka, van Es, Michael A, Koppers, Max, van Rheenen, Wouter, Medic, Jelena, Schelhaas, Helenius J, van der Kooi, Anneke J, de Visser, Marianne, Veldink, Jan H, van den Berg, Leonard H

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Less-Invasive Approach to Early-Onset Scoliosis-Surgical Technique for Magnetically Controlled Growing Rod (MCGR) Based on Treatment of 2-Year-Old Child with Severe Scoliosis von Grabala, Pawel, Helenius, Ilkka J, Chamberlin, Kelly, Galgano, Michael

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Progesterone Inhibition of Wnt/β-Catenin Signaling in Normal Endometrium and Endometrial Cancer von YONGYI WANG, HANIFI-MOGHADDAM, Payman, BURGER, Curt W, FODDE, Riccardo, BLOK, Leen J, HANEKAMP, Eline E, KLOOSTERBOER, Helenius J, FRANKEN, Patrick, VELDSCHOLTE, Jos, VAN DOORN, Helena C, EWING, Patricia C, KIM, J. Julie, GROOTEGOED, J. Anton

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VCP mutations in familial and sporadic amyotrophic lateral sclerosis von Koppers, Max, van Blitterswijk, Marka M, Vlam, Lotte, Rowicka, Paulina A, van Vught, Paul W.J, Groen, Ewout J.N, Spliet, Wim G.M, Engelen-Lee, JooYeon, Schelhaas, Helenius J, de Visser, Marianne, van der Kooi, Anneke J, van der Pol, W-Ludo, Pasterkamp, R. Jeroen, Veldink, Jan H, van den Berg, Leonard H

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Genetic overlap between apparently sporadic motor neuron diseases von van Blitterswijk, Marka, Vlam, Lotte, van Es, Michael A, van der Pol, W-Ludo, Hennekam, Eric A M, Dooijes, Dennis, Schelhaas, Helenius J, van der Kooi, Anneke J, de Visser, Marianne, Veldink, Jan H, van den Berg, Leonard H

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Euthanasia and physician-assisted suicide in amyotrophic lateral sclerosis: a prospective study von Maessen, Maud, Veldink, Jan H., Onwuteaka-Philipsen, Bregje D., Hendricks, Henk T., Schelhaas, Helenius J., Grupstra, Hepke F., van der Wal, Gerrit, van den Berg, Leonard H.

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