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Judith van Gaalen
Judith van Gaalen
Neuroloog | Rijnstate Ziekenhuis & Radboudumc Expertisecentrum Parkinson en Bewegingsstoornissen
在 radboudumc.nl 的电子邮件经过验证
标题
引用次数
引用次数
年份
Movement disorders in spinocerebellar ataxias
J van Gaalen, P Giunti, BP van de Warrenburg
Movement Disorders 26 (5), 792-800, 2011
1582011
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
1332014
The preclinical stage of spinocerebellar ataxias
RP Maas, J van Gaalen, T Klockgether, BPC van de Warrenburg
Neurology 85 (1), 96-103, 2015
1252015
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
792020
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
742020
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
682014
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
612017
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
422021
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
392012
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
382019
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
352018
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
342019
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
242019
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
222021
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
222019
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
212019
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
192022
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
192015
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
182020
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
172022
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