Movement disorders in spinocerebellar ataxias J van Gaalen, P Giunti, BP van de Warrenburg Movement Disorders 26 (5), 792-800, 2011 | 158 | 2011 |
EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood BPC Van de Warrenburg, J Van Gaalen, S Boesch, JM Burgunder, A Dürr, ... European journal of neurology 21 (4), 552-562, 2014 | 133 | 2014 |
The preclinical stage of spinocerebellar ataxias RP Maas, J van Gaalen, T Klockgether, BPC van de Warrenburg Neurology 85 (1), 96-103, 2015 | 125 | 2015 |
Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice C Wilke, E Haas, K Reetz, J Faber, H Garcia‐Moreno, MM Santana, ... EMBO molecular medicine 12 (7), e11803, 2020 | 79 | 2020 |
KIF1A variants are a frequent cause of autosomal dominant hereditary spastic paraplegia M Pennings, MI Schouten, J van Gaalen, RPP Meijer, ST de Bot, M Kriek, ... European Journal of Human Genetics 28 (1), 40-49, 2020 | 74 | 2020 |
Drug-induced cerebellar ataxia: a systematic review J Van Gaalen, FG Kerstens, R Maas, L Härmark, BPC van de Warrenburg CNS drugs 28, 1139-1153, 2014 | 68 | 2014 |
Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia I Giordano, F Harmuth, H Jacobi, B Paap, S Vielhaber, J Machts, L Schöls, ... Neurology 89 (10), 1043-1049, 2017 | 61 | 2017 |
Regional brain and spinal cord volume loss in spinocerebellar ataxia type 3 J Faber, T Schaprian, K Berkan, K Reetz, MC França Jr, TJR de Rezende, ... Movement disorders 36 (10), 2273-2281, 2021 | 42 | 2021 |
A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into order J van Gaalen, BPC van de Warrenburg Practical neurology 12 (1), 14-24, 2012 | 39 | 2012 |
Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy MS van Der Knaap, M Bugiani, MI Mendes, LG Riley, DEC Smith, ... Neurology 92 (11), e1225-e1237, 2019 | 38 | 2019 |
Heterozygous missense variants of LMX1A lead to nonsyndromic hearing impairment and vestibular dysfunction M Wesdorp, PAM de Koning Gans, M Schraders, J Oostrik, MA Huynen, ... Human genetics 137, 389-400, 2018 | 35 | 2018 |
Genotype–phenotype correlations in ataxia telangiectasia patients with ATM c. 3576G> A and c. 8147T> C mutations NJH van Os, L Chessa, CMR Weemaes, M van Deuren, A Fiévet, ... Journal of Medical Genetics 56 (5), 308-316, 2019 | 34 | 2019 |
The movement disorder spectrum of SCA21 (ATX-TMEM240): 3 novel families and systematic review of the literature A Traschütz, J van Gaalen, M Oosterloo, M Vreeburg, EJ Kamsteeg, ... Parkinsonism & related disorders 62, 215-220, 2019 | 24 | 2019 |
Polyglutamine‐expanded Ataxin‐3: a target engagement marker for spinocerebellar ataxia type 3 in peripheral blood J Hübener‐Schmid, K Kuhlbrodt, J Peladan, J Faber, MM Santana, ... Movement Disorders 36 (11), 2675-2681, 2021 | 22 | 2021 |
De novo SPAST mutations may cause a complex SPG4 phenotype JH Schieving, ST de Bot, LA van de Pol, NI Wolf, EH Brilstra, SG Frints, ... Brain 142 (7), e31-e31, 2019 | 22 | 2019 |
Abnormal eyeblink conditioning is an early marker of cerebellar dysfunction in preclinical SCA3 mutation carriers J van Gaalen, R Maas, EF Ippel, MW Elting, KY van Spaendonck-Zwarts, ... Experimental brain research 237, 427-433, 2019 | 21 | 2019 |
Digital gait biomarkers allow to capture 1‐year longitudinal change in spinocerebellar ataxia type 3 W Ilg, B Müller, J Faber, J van Gaalen, H Hengel, IR Vogt, G Hennes, ... Movement Disorders 37 (11), 2295-2301, 2022 | 19 | 2022 |
A single session of cerebellar theta burst stimulation does not alter writing performance in writer’s cramp MW Linssen, J van Gaalen, MAM Munneke, BS Hoffland, W Hulstijn, ... Brain 138 (6), e355-e355, 2015 | 19 | 2015 |
Classic ataxia-telangiectasia: the phenotype of long-term survivors NJH van Os, M van Deuren, CMR Weemaes, J van Gaalen, H Hijdra, ... Journal of Neurology 267, 830-837, 2020 | 18 | 2020 |
Differential temporal dynamics of axial and appendicular ataxia in SCA3 RP Maas, S Teerenstra, M Lima, P Pires, L Pereira de Almeida, ... Movement Disorders 37 (9), 1850-1860, 2022 | 17 | 2022 |