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Full Text	Issue Date	Title	Author(s)
	2012	Cerebellar Cognitive Affective Syndrome and Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: A Report of Two Male Sibs	Verhoeven, W.M.A.; Egger, J.I.M.; Ahmed, A.I.A.; Kremer, H.P.H.; Vermeer, S.; Warrenburg, B.P.C. van de
	2012	Reduced parietal connectivity with a premotor writing area in writer's cramp	Delnooz, C.C.S.; Helmich, R.C.G.; Toni, I.; Warrenburg, B.P.C. van de
	2012	Compensatory Activity in the Extrastriate Body Area of Parkinson's Disease Patients	Nuenen, B.F.L. van; Helmich, R.C.G.; Buenen, N.; Warrenburg, B.P.C. van de; Bloem, B.R.; Toni, I.
	2012	Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism	Nuenen, B.F.L. van; Helmich, R.C.G.; Ferraye, M.; Thaler, A.; Hendler, T.; Orr-Urtreger, A.; Mirelman, A.; Bressman, S.; Marder, K.S.; Giladi, N.; Warrenburg, B.P.C. van de; Bloem, B.R.; Toni, I.
	2011	Genetics of the dominant ataxias.	Verbeek, D.S.; Warrenburg, B.P.C. van de
	2011	Ataxia telangiectasia: the consequences of a delayed diagnosis	Mandigers, C.M.P.W.; Warrenburg, B.P.C. van de; Strobbe, L.J.; Kluijt, I.; Molenaar, A.H.; Schinagl, D.A.X.
	2011	Postural deformities in Parkinson's disease	Doherty, K.M.; Warrenburg, B.P.C. van de; Peralta, M.C.; Silveira-Moriyama, L.; Azulay, J.P.; Gershanik, O.S.; Bloem, B.R.
	2011	A distinctive pattern of cortical excitability in patients with the syndrome of dystonia and cerebellar ataxia	Talelli, P.; Hoffland, B.S.; Schneider, S.A.; Edwards, M.; Bhatia, K.P.; Warrenburg, B.P.C. van de; Rothwell, J.C.
	2011	Kleefstra Syndrome in Three Adult Patients: Further Delineation of the Behavioral and Neurological Phenotype Shows Aspects of a Neurodegenerative Course	Verhoeven, W.M.A.; Egger, J.I.M.; Vermeulen, K.; Warrenburg, B.P.C. van de; Kleefstra, T.
	2011	Patients with primary cervical dystonia have evidence of discrete deficits in praxis	Hoffland, B.S.; Snik, D.; Bhatia, K.P.; Baratelli, E.; Katschnig, P.; Schwingenschuh, P.; Crutch, S.; Warrenburg, B.P.C. van de; Edwards, M.J.
	2011	Cerebellar brain inhibition is decreased in active and surround muscles at the onset of voluntary movement	Kassavetis, P.; Hoffland, B.S.; Saifee, T.A.; Bhatia, K.P.; Warrenburg, B.P.C. van de; Rothwell, J.C.; Edwards, M.
	2011	Genome-wide association study confirms extant PD risk loci among the Dutch	Simon-Sanchez, J.; Hilten, J.J. van; Warrenburg, B.P.C. van de; Post, B.; Berendse, H.W.; Arepalli, S.; Hernandez, D.G.; Bie, R.M. de; Velseboer, D.; Scheffer, H.; Bloem, B.R.; Dijk, K.D. van; Rivadeneira, F.; Hofman, A.; Uitterlinden, A.G.; Rizzu, P.; Bochdanovits, Z.; Singleton, A.B.; Heutink, P.
	2011	How might physical activity benefit patients with Parkinson disease?	Speelman, A.D.; Warrenburg, B.P.C. van de; Nimwegen, M.L. van; Petzinger, G.M.; Munneke, M.; Bloem, B.R.
	2011	Movement disorders in spinocerebellar ataxias	Gaalen, J. van; Giunti, P.; Warrenburg, B.P.C. van de
	2011	Adult metachromatic leukodystrophy treated by allo-SCT and a review of the literature	Hosson, L.D. de; Warrenburg, B.P.C. van de; Preijers, F.W.M.B.; Blijlevens, N.M.A.; Reijden, B.A. van der; Kremer, H.P.H.; Lefeber, D.J.; Allebes, W.A.; Al-Ali, H.; Niederwieser, D.W.; Schaap, N.P.M.; Schattenberg, A.V.M.B.
	2011	Botulinum toxin has an increased effect when targeted toward the muscle's endplate zone: a high-density surface EMG guided study	Lapatki, B.G.; Dijk, J.P. van; Warrenburg, B.P.C. van de; Zwarts, M.J.
	2011	Autosomal recessive cerebellar ataxias: the current state of affairs	Vermeer, S.; Warrenburg, B.P.C. van de; Willemsen, M.A.A.P.; Cluitmans, M.; Scheffer, H.; Kremer, B.; Knoers, N.V.A.M.
	2011	Kleefstra syndrome in three adult patients: further delineation of the behavioral and neurological phenotype shows aspects of a neurodegenerative course	Verhoeven, W.M.A.; Egger, J.I.; Vermeulen, K.; Warrenburg, B.P.C. van de; Kleefstra, T.
	2011	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies	Nalls, M.A.; Plagnol, V.; Hernandez, D.G.; Sharma, M.; Sheerin, U.M.; Saad, M.; Simon-Sanchez, J.; Schulte, C.; Lesage, S.; Sveinbjornsdottir, S.; Stefansson, K.; Martinez, M.; Hardy, J.; Heutink, P.; Brice, A.; Gasser, T.; Singleton, A.B.; Wood, N.W.; Bloem, B.R.; Post, B.; Scheffer, H.; Warrenburg, B.P.C. van de
	2011	Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations	Elfferich, P.; Verleun-Mooijman, M.C.T.; Maat-Kievit, J.A.; Warrenburg, B.P.C. van de; Abdo, W.F.; Eshuis, S.A.; Leenders, K.L.; Hovestadt, A.; Zijlmans, J.C.M.; Stroy, J.P.; Swieten, J.C. van; Boon, A.J.; Engelen, K. van; Verschuuren-Bemelmans, C.C.; Lesnik-Oberstein, S.A.; Tassorelli, C.; Lopiano, L.; Bonifati, V.; Dooijes, D.; Minkelen, R. van
	2011	The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study	Jacobi, H.; Bauer, P.; Giunti, P.; Labrum, R.; Sweeney, M.G.; Charles, P.; Durr, A.; Marelli, C.; Globas, C.; Linnemann, C.; Schols, L.; Rakowicz, M.; Rola, R.; Zdzienicka, E.; Schmitz-Hubsch, T.; Fancellu, R.; Mariotti, C.; Tomasello, C.; Baliko, L.; Melegh, B.; Filla, A.; Rinaldi, C.; Warrenburg, B.P.C. van de; Verstappen, C.C.P.; Szymanski, S.; Berciano, J.; Infante, J.; Timmann, D.; Boesch, S.; Hering, S.; Depondt, C.; Pandolfo, M.; Kang, J.S.; Ratzka, S.; Schulz, J.; Tezenas du Montcel, S.; Klockgether, T.
	2011	Depression comorbidity in spinocerebellar ataxia	Schmitz-Hubsch, T.; Coudert, M.; Tezenas du Montcel, S.; Giunti, P.; Labrum, R.; Durr, A.; Ribai, P.; Charles, P.; Linnemann, C.; Schols, L.; Rakowicz, M.; Rola, R.; Zdzienicka, E.; Fancellu, R.; Mariotti, C.; Baliko, L.; Melegh, B.; Filla, A.; Salvatore, E.; Warrenburg, B.P.C. van de; Szymanski, S.; Infante, J.; Timmann, D.; Boesch, S.; Depondt, C.; Kang, J.S.; Schulz, J.B.; Klopstock, T.; Lossnitzer, N.; Lowe, B.; Frick, C.; Rottlander, D.; Schlaepfer, T.E.; Klockgether, T.
	2011	Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.	Es, M.A. van; Schelhaas, H.J.; Vught, P.W. van; Ticozzi, N.; Andersen, P.M.; Groen, E.J.; Schulte, C.; Blauw, H.M.; Koppers, M.; Diekstra, F.P.; Fumoto, K.; Leclerc, A.L.; Keagle, P.; Bloem, B.R.; Scheffer, H.; Nuenen, B.F.L. van; Blitterswijk, M. van; Rheenen, W. van; Wills, A.M.; Lowe, P.P.; Hu, G.F.; Yu, W.; Kishikawa, H.; Wu, D.; Folkerth, R.D.; Mariani, C.; Goldwurm, S.; Pezzoli, G.; Damme, P. van; Lemmens, R.; Dahlberg, C.; Birve, A.; Fernandez-Santiago, R.; Waibel, S.; Klein, C.; Weber, M.; Kooi, A.J. van der; Visser, M.C.H. de; Verbaan, D.; Hilten, J.J. van; Heutink, P.; Hennekam, E.A.; Cuppen, E.; Berg, D. Van den; Brown, R.H. Jr.; Silani, V.; Gasser, T.; Ludolph, A.C.; Robberecht, W.; Ophoff, R.A.; Veldink, J.H.; Pasterkamp, R.J.; Bakker, P.I. de; Landers, J.E.; Warrenburg, B.P.C. van de; Berg, L.H. van den
	2011	A two-stage meta-analysis identifies several new loci for Parkinson's disease.	Plagnol, V.; Nalls, M.A.; Bras, J.M.; Hernandez, D.; Sharma, M.; Sheerin, U.M.; Saad, M.; Simon-Sanchez, J.; Schulte, C.; Lesage, S.; Sveinbjornsdottir, S.; Amouyel, P.; Arepalli, S.; Band, G.; Barker, R.A.; Bellinguez, C.; Ben-Shlomo, Y.; Berendse, H.W.; Berg, D.; Bhatia, K.P.; Bie, R.M. de; Biffi, A.; Bloem, B.R.; Bochdanovits, Z.; Bonin, M.; Brockmann, K.; Brooks, J.; Burn, D.J.; Charlesworth, G.; Chen, H.; Chinnery, P.F.; Chong, S.; Clarke, C.E.; Cookson, M.R.; Cooper, J.M.; Corvol, J.C.; Counsell, J.; Damier, P.; Dartigues, J.F.; Deloukas, P.; Deuschl, G.; Dexter, D.T.; Dijk, K.D. van; Dillman, A.; Durif, F.; Durr, A.; Edkins, S.; Evans, J.R.; Foltynie, T.; Freeman, C.; Gao, J.; Gardner, M.; Gibbs, J.R.; Goate, A.; Gray, E.; Guerreiro, R.; Gustafsson, O.; Harris, C.; Hellenthal, G.; Hilten, J.J. van; Hofman, A.; Hollenbeck, A.; Holton, J.L.; Hu, M.; Huang, X.; Huber, H.; Hudson, G.; Hunt, S.E.; Huttenlocher, J.; Illig, T.; Jonsson, P.V.; Langford, C.; Lees, A.J.; Lichtner, P.; Limousin, P.; Lopez, G.; McNeill, A.; Moorby, C.; Moore, M.; Morris, H.A.; Morrison, K.E.; Mudanohwo, E.; O'Sullivan, S.S; Pearson, J.; Pearson, R.; Perlmutter, J.; Petursson, H.; Pirinen, M.; Polnak, P.; Post, B.; Potter, S.C.; Ravina, B.; Revesz, T.; Riess, O.; Rivadeneira, F.; Rizzu, P.; Ryten, M.; Sawcer, S.J.; Schapira, A.; Scheffer, H.; Shaw, K.; Shoulson, I.; Sidransky, E.; Silva, R. de; Smith, C.; Spencer, C.C.; Stefansson, H.; Steinberg, S.; Stockton, J.D.; Strange, A.; Su, Z.; Talbot, K.; Tanner, C.M.; Tashakkori-Ghanbaria, A.; Tison, F.; Trabzuni, D.; Traynor, B.J.; Uitterlinden, A.G.; Vandrovcova, J.; Velseboer, D.; Vidailhet, M.; Vukcevic, D.; Walker, R.; Warrenburg, B.P.C. van de; Weale, M.E.; Wickremaratchi, M.; Williams, N.; Williams-Gray, C.H.; Winder-Rhodes, S.; Stefansson, K.; Martinez, M.; Donnelly, P.; Singleton, A.B.; Hardy, J.; Heutink, P.; Brice, A.; Gasser, T.; Wood, N.W.
	2010	Het fragiele-X-geassocieerde tremor-ataxie syndroom (FXTAS)	Vossen, P. van der; Gons, R.A.R.; Bloem, B.R.; Verschuuren-Bemelmans, C.C.; Warrenburg, B.P.C. van de
	2010	Child neurology: hereditary spastic paraplegia in children.	Bot, S.T. de; Warrenburg, B.P.C. van de; Kremer, H.P.H.; Willemsen, M.A.A.P.
	2010	Validation of a dystonia screening questionnaire: testing in a cohort of mixed neurological disorders.	Snik, D.M.; Hoffland, B.S.; Aguirregomozcorta, M.; Schwingenschuh, P.; Bhatia, K.P.; Warrenburg, B.P.C. van de; Edwards, M.J.R.
	2010	Een ernstige, subacute axonale polyneuropathie door hypofosfatemie	Eijk, J.J.J. van; Abdo, W.; Deurwaarder, E. den; Zwarts, M.J.; Warrenburg, B.P.C. van de
	2010	The clinical approach to movement disorders.	Abdo, W.; Warrenburg, B.P.C. van de; Burn, D.J.; Quinn, N.P.; Bloem, B.R.
	2010	Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.	Bot, S.T. de; Elzen, R.T. van den; Mensenkamp, A.R.; Schelhaas, H.J.; Willemsen, M.A.A.P.; Knoers, N.V.A.M.; Kremer, H.P.H.; Warrenburg, B.P.C. van de; Scheffer, H.
	2010	DYT6 dystonia: mutation screening, phenotype, and response to deep brain stimulation.	Groen, J.L.; Ritz, K.; Contarino, M.F.; Warrenburg, B.P.C. van de; Aramideh, M.; Foncke, E.M.; Hilten, J.J. van; Schuurman, P.R.; Speelman, J.D.; Koelman, J.H.; Bie, R.M. de; Baas, F.; Tijssen, M.A.
	2010	Nonmotor symptoms in Parkin gene-related parkinsonism.	Kagi, G.; Klein, C.; Wood, N.W.; Schneider, S.A.; Pramstaller, P.P.; Tadic, V.; Quinn, N.P.; Warrenburg, B.P.C. van de; Bhatia, K.P.
	2010	New cases of adult-onset Sandhoff disease with a cerebellar or lower motor neuron phenotype.	Delnooz, C.C.S.; Lefeber, D.J.; Langemeijer, S.M.C.; Hoffjan, S.; Dekomien, G.; Zwarts, M.J.; Engelen, B.G.M. van; Wevers, R.A.; Schelhaas, H.J.; Warrenburg, B.P.C. van de
	2010	Pallidopyramidal disease : a misnomer?	Horstink, M.W.I.M.; Dekker, M.C.J.; Montagna, P.; Bonifati, V.; Warrenburg, B.P.C. van de
	2010	Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.	Schulz, J.B.; Borkert, J.; Wolf, S.; Schmitz-Hubsch, T.; Rakowicz, M.; Mariotti, C.; Schols, L.; Timmann, D.; Warrenburg, B.P.C. van de; Durr, A.; Pandolfo, M.; Kang, J.S.; Mandly, A.G.; Nagele, T.; Grisoli, M.; Boguslawska, R.; Bauer, P.; Klockgether, T.; Hauser, T.K.
	2010	Responsiveness of different rating instruments in spinocerebellar ataxia patients.	Schmitz-Hubsch, T.; Fimmers, R.; Rakowicz, M.; Rola, R.; Zdzienicka, E.; Fancellu, R.; Mariotti, C.; Linnemann, C.; Schols, L.; Timmann, D.; Filla, A.; Salvatore, E.; Infante, J.; Giunti, P.; Labrum, R.; Kremer, B.; Warrenburg, B.P.C. van de; Baliko, L.; Melegh, B.; Depondt, C.; Schulz, J.; Montcel, S.T. du; Klockgether, T.
	2010	Falls in spinocerebellar ataxias: Results of the EuroSCA Fall Study.	Fonteyn, E.M.; Schmitz-Hubsch, T.; Verstappen, C.C.P.; Baliko, L.; Bloem, B.R.; Boesch, S.; Bunn, L.; Charles, P.; Durr, A.; Filla, A.; Giunti, P.; Globas, C.; Klockgether, T.; Melegh, B.; Pandolfo, M.; Rosa, A. De; Schols, L.; Timmann, D.; Munneke, M.; Kremer, H.P.H.; Warrenburg, B.P.C. van de
	2010	Self-rated health status in spinocerebellar ataxia--results from a European multicenter study.	Schmitz-Hubsch, T.; Coudert, M.; Giunti, P.; Globas, C.; Baliko, L.; Fancellu, R.; Mariotti, C.; Filla, A.; Rakowicz, M.; Charles, P.; Ribai, P.; Szymanski, S.; Infante, J.; Warrenburg, B.P.C. van de; Durr, A.; Timmann, D.; Boesch, S.; Rola, R.; Depondt, C.; Schols, L.; Zdzienicka, E.; Kang, J.S.; Ratzka, S.; Kremer, B.; Schulz, J.B.; Klopstock, T.; Melegh, B.; Montcel, S.T. du; Klockgether, T.
	2010	Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.	Vermeer, S.; Hoischen, A.; Meijer, R.P.; Gilissen, C.F.H.A.; Neveling, K.; Wieskamp, N.A.W.; Brouwer, A.; Koenig, M.; Anheim, M.; Assoum, M.; Drouot, N.; Todorovic, S.; Milic-Rasic, V.; Lochmuller, H.; Stevanin, G.; Goizet, C.; David, A.; Durr, A.; Brice, A.; Kremer, B.; Warrenburg, B.P.C. van de; Schijvenaars, M.M.V.A.P.; Heister, A.; Kwint, M.P.; Arts, P.J.W.; Wijst, J.A.J. van der; Veltman, J.; Kamsteeg, E.J.; Scheffer, H.; Knoers, N.V.A.M.
	2009	There might be more to SPG4!	Warrenburg, B.P.C. van de
	2009	Seipin/BSCL2 mutation screening in sporadic adult-onset upper motor neuron syndromes.	Brugman, F.; Scheffer, H.; Schelhaas, H.J.; Nillesen, W.M.; Wokke, J.H.J.; Warrenburg, B.P.C. van de; Berg, L.H. van den
	2009	Hereditaire spastische paraparesen : stand van zaken en leidraad voor genetisch onderzoek	Bot, S.T. de; Scheffer, H.; Schelhaas, H.J.; Knoers, N.V.A.M.; Willemsen, M.A.A.P.; Warrenburg, B.P.C. van de; Kremer, H.P.H.
	2009	Atypical dystonic shoulder movements following neuralgic amyotrophy.	Abdo, W.; Bloem, B.R.; Eijk, J.J.J. van; Geurts, A.C.H.; Alfen, N. van; Warrenburg, B.P.C. van de
	2009	ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia (vol 9, pg 207, 2008)	Vermeer, S.; Meijer, R.P.; Pijl, B.J.; Timmermans, J.; Cruysberg, J.R.M.; Bos, M.M.; Schelhaas, H.J.; Warrenburg, B.P.C. van de; Knoers, N.V.A.M.; Scheffer, H.; Kremer, H.P.H.
	2009	Repetitive transcranial magnetic stimulation for levodopa-induced dyskinesias in Parkinson's disease.	Filipovic, S.R.; Rothwell, J.C.; Warrenburg, B.P.C. van de; Bhatia, K.P.
	2009	Clinical identification of dysarthria types among neurologists, residents in neurology and speech therapists.	Graaff, M. Van der; Kuiper, T.; Zwinderman, A.; Warrenburg, B.P.C. van de; Poels, P.J.E.; Offeringa, A.; Kooi, A. van der; Speelman, H.D.; Visser, M. de
	2009	Neurophysiological evidence for cerebellar dysfunction in primary focal dystonia.	Teo, J.T.; Warrenburg, B.P.C. van de; Schneider, S.A.; Rothwell, J.C.; Bhatia, K.P.
	2009	Paramedical treatment in primary dystonia: a systematic review.	Delnooz, C.C.S.; Horstink, M.W.I.M.; Tijssen, M.A.; Warrenburg, B.P.C. van de
	2009	Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.	Schule, R.; Bonin, M.; Durr, A.; Forlani, S.; Sperfeld, A.D.; Klimpe, S.; Mueller, J.C.; Seibel, A.; Warrenburg, B.P.C. van de; Bauer, P.; Schols, L.
	2009	Postural instability in cerebellar ataxia: correlations of knee, arm and trunk movements to center of mass velocity.	Kung, U.M.; Horlings, C.G.; Honegger, F.; Kremer, H.P.H.; Bloem, B.R.; Warrenburg, B.P.C. van de; Allum, J.H.J.

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