Mutation in the SYNJ1 Gene Associated with Autosomal Recessive, Early-Onset Parkinsonism von Quadri, Marialuisa, Fang, Mingyan, Picillo, Marina, Olgiati, Simone, Breedveld, Guido J., Graafland, Josja, Wu, Bin, Xu, Fengping, Erro, Roberto, Amboni, Marianna, Pappatà, Sabina, Quarantelli, Mario, Annesi, Grazia, Quattrone, Aldo, Chien, Hsin F., Barbosa, Egberto R., Oostra, Ben A., Barone, Paolo, Wang, Jun, Bonifati, Vincenzo

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How do the benefits from active demand vary? A comparison of four EU countries von Cronenberg, A., Delnooz, A., Linke, C., Baron, M., Lago, O., Linares, P.

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e-Harbours: Identification and analysis of barriers for Virtual Power Plants in harbour regions von Delnooz, A., Six, D., Kessels, K., Hommelberg, M. P. F.

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Task-free functional MRI in cervical dystonia reveals multi-network changes that partially normalize with botulinum toxin von Delnooz, Cathérine C S, Pasman, Jaco W, Beckmann, Christian F, van de Warrenburg, Bart P C

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Network localization of cervical dystonia based on causal brain lesions von Corp, Daniel T, Joutsa, Juho, Darby, R Ryan, Delnooz, Cathérine C S, van de Warrenburg, Bart P C, Cooke, Danielle, Prudente, Cecília N, Ren, Jianxun, Reich, Martin M, Batla, Amit, Bhatia, Kailash P, Jinnah, Hyder A, Liu, Hesheng, Fox, Michael D

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Altered striatal and pallidal connectivity in cervical dystonia von Delnooz, Cathérine C. S., Pasman, Jaco W., Beckmann, Christian F., van de Warrenburg, Bart P. C.

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A Gain‐of‐Function Variant in Dopamine D2 Receptor and Progressive Chorea and Dystonia Phenotype von Weijden, Marlous C.M., Rodriguez‐Contreras, Dayana, Delnooz, Cathérine C.S., Robinson, Brooks G., Condon, Alec F., Kielhold, Michelle L., Stormezand, Gilles N., Ma, Kai Yu, Dufke, Claudia, Williams, John T., Neve, Kim A., Tijssen, Marina A.J., Verbeek, Dineke S.

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Dynamic cortical gray matter volume changes after botulinum toxin in cervical dystonia von Delnooz, Cathérine C.S, Pasman, Jaco W, van de Warrenburg, Bart P.C

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The cost-effectiveness of specialized nursing interventions for people with Parkinson's disease: the NICE-PD study protocol for a randomized controlled clinical trial von Radder, Danique L M, Lennaerts, Herma H, Vermeulen, Hester, van Asseldonk, Thies, Delnooz, Cathérine C S, Hagen, Rob H, Munneke, Marten, Bloem, Bastiaan R, de Vries, Nienke M

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Reduced parietal connectivity with a premotor writing area in writer's cramp von Delnooz, Cathérine C.S., Helmich, Rick C., Toni, Ivan, van de Warrenburg, Bart P.C.

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Writer's cramp: Increased dorsal premotor activity during intended writing von Delnooz, Cathérine C.S., Helmich, Rick C., Medendorp, W.P., Van de Warrenburg, Bart P.C., Toni, Ivan

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Expanding the phenotype in aminoacylase 1 (ACY1) deficiency: characterization of the molecular defect in a 63-year-old woman with generalized dystonia von Sass, Jörn Oliver, Vaithilingam, Jathana, Gemperle-Britschgi, Corinne, Delnooz, Cathérine C. S., Kluijtmans, Leo A. J., van de Warrenburg, Bart P. C., Wevers, Ron A.

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Using the shared genetics of dystonia and ataxia to unravel their pathogenesis von Nibbeling, Esther A.R., Delnooz, Cathérine C.S., de Koning, Tom J., Sinke, Richard J., Jinnah, Hyder A., Tijssen, Marina A.J., Verbeek, Dineke S.

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Paramedical treatment in primary dystonia: A systematic review von Delnooz, Cathérine C.S., Horstink, Martin W.I.M., Tijssen, Marina A., van de Warrenburg, Bart P.C.

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Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease von Quadri, Marialuisa, Federico, Antonio, Zhao, Tianna, Breedveld, Guido J., Battisti, Carla, Delnooz, Cathérine, Severijnen, Lies-Anne, Di Toro Mammarella, Lara, Mignarri, Andrea, Monti, Lucia, Sanna, Antioco, Lu, Peng, Punzo, Francesca, Cossu, Giovanni, Willemsen, Rob, Rasi, Fabrizio, Oostra, Ben A., van de Warrenburg, Bart P., Bonifati, Vincenzo

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Disease impact in chronic progressive external ophthalmoplegia: More than meets the eye von Smits, Bart W, Fermont, Jiske, Delnooz, Cathérine C.S, Kalkman, Joke S, Bleijenberg, Gijs, van Engelen, Baziel G.M

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Projet pour le nº 17 / 2024 von Delnooz, Isabelle

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Phenotypic variability in a dystonia family with mutations in the manganese transporter gene von Delnooz, Cathérine C. S., Wevers, Ron A., Quadri, Marialuisa, Clayton, Peter T., Mills, Philippa B., Tuschl, Karin, Steenbergen, Eric J., Bonifati, Vincenzo, van de Warrenburg, Bart P. C.

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Addressing creativity in higher education from a rhizomatic perspective von de Vries, E.W., Delnooz, P., Velthuijsen, H., Pinxten, R.

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Current and future medical treatment in primary dystonia von Delnooz, Cathérine C.S., van de Warrenburg, Bart P.C.

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