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Martin W.I.M. Horstink

Observed names: M W Horstink, M W I Horstink, M W I M Horstink, M. H. I. M. Horstink, M. Horstink, M. W I M Horstink, M. W. Horstink, M. W. I. Horstink, M. W. I. M. Horstink, M. W. M. Horstink, M. W.I.M. Horstink, M.W. Horstink, M.W. I. M. Horstink, M.W.I. Horstink, M.W.I.M Horstink, M.W.I.M. Horstink, M.W.J.M. Horstink, Martin Horstink, Martin W I M Horstink, Martin W. Horstink, Martin W. I. M. Horstink, Martin W.I. Horstink, Martin W.I.M Horstink, Martin WIM Horstink
Observed institutions: Radboud University Nijmegen, Inserm, Universidade de São Paulo, University of Milan, Erasmus MC, Amsterdam UMC Location University of Amsterdam, Radboud University Medical Center, Max Planck Institute for Psycholinguistics, Hospital de Clínicas de Porto Alegre, Canisius-Wilhelmina Ziekenhuis, National Hospital for Neurology and Neurosurgery, Institut für Medizinische Psychologie, UCL Queen Square Institute of Neurology, Donders Institute for Brain, Cognition and Behaviour, Donders Centre for Neuroscience, Physiopathologie des Comportements, University of Turin, University of Bari Aldo Moro, Sapienza University of Rome
OpenAlex ID: A5109802377
Gender differences in Parkinson's disease
2006 · C. A Haaxma, B. R Bloem, et al. · Journal of Neurology Neurosurgery & Psychiatry · 795
Accurate differentiation of parkinsonism and essential tremor using visual assessment of [123I]-FP-CIT SPECT imaging: The [123I]-FP-CIT study group
2000 · Hani T. S. Benamer, Jim Patterson, et al. · Movement Disorders · 699
PARK7, a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism, on Chromosome 1p36
2001 · C.M. van Duijn, M.C.J. Dekker, et al. · The American Journal of Human Genetics · 385
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Cognitive and motor shifting aptitude disorder in Parkinson's disease.
1984 · A R Cools, J H van den Bercken, et al. · Journal of Neurology Neurosurgery & Psychiatry · 370
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FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndrome
2008 · A. Di Fonzo, M.C.J. Dekker, et al. · Neurology · 362
Early-onset parkinsonism associated with PINK1 mutations
2005 · V. Bonifati, C. F. Rohé, et al. · Neurology · 342
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
2007 · A. Di Fonzo, H. F. Chien, et al. · Neurology · 337
How much phenotypic variation can be attributed to parkin genotype?
2003 · Ebba Lohmann, Magali Periquet, et al. · Annals of Neurology · 304
Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies and the Movement Disorder Society–European Section. Part I: early (uncomplicated) Parkinson's disease
2006 · M. Horstink, E. Tolosa, et al. · European Journal of Neurology · 297
The clinical benefit of imaging striatal dopamine transporters with [123I]FP-CIT SPET in differentiating patients with presynaptic parkinsonism from those with other forms of parkinsonism
2001 · Jan Booij, Johannes D. Speelman, et al. · European Journal of Nuclear Medicine and Molecular Imaging · 264
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations
2001 · B.P.C. van de Warrenburg, M. Lammens, et al. · Neurology · 257
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Symptoms and duration of the prodromal phase in parkinson's disease
1997 · Ed G. Gonera, Martin Van't Hof, et al. · Movement Disorders · 215
Review of the therapeutic management of Parkinson's disease. Report of a joint task force of the European Federation of Neurological Societies (EFNS) and the Movement Disorder Society‐European Section (MDS‐ES). Part II: late (complicated) Parkinson's disease
2006 · M. Horstink, E. Tolosa, et al. · European Journal of Neurology · 173
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Ambulatory motor assessment in Parkinson's disease
2005 · Noël L.W. Keijsers, Martin W.I.M. Horstink, et al. · Movement Disorders · 158
Dipole source analysis suggests selective modulation of the supplementary motor area contribution to the readiness potential
1996 · P. Praamstra, D.F. Stegeman, et al. · Electroencephalography and Clinical Neurophysiology · 151
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Automatic assessment of levodopa‐induced dyskinesias in daily life by neural networks
2002 · Noël L.W. Keijsers, Martin W.I.M. Horstink, et al. · Movement Disorders · 138
MRI in patients with suspected vascular parkinsonism
1995 · J.C.M. Zijlmans, H.O.M. Thijssen, et al. · Neurology · 118
Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects
2001 · Magali Periquet, Christoph B. Lücking, et al. · The American Journal of Human Genetics · 112
Memory and learning strategies in patients with Parkinson's disease
1994 · Elly L. Buytenhuijs, Hans J.C. Berger, et al. · Neuropsychologia · 112
Estrogen as Neuroprotectant of Nigrostriatal Dopaminergic System: Laboratory and Clinical Studies
2003 · Dean E. Dluzen, Martin W. I. M. Horstink · Endocrine · 105
Intermediate CAG repeat lengths (53,54) for MJD/SCA3 are associated with an abnormal phenotype
2001 · Nens Van Alfen, Richard J. Sinke, et al. · Annals of Neurology · 101
Effects of Female Sex Steroids on Parkinsonʼs Disease in Postmenopausal Women
1999 · Elma Strijks, Jan A. M. Kremer, et al. · Clinical Neuropharmacology · 95
Genetic and environmental risk factors in Parkinson’s disease
1998 · B.A.J Veldman, A.M Wijn, et al. · Clinical Neurology and Neurosurgery · 92
Cerebrospinal fluid analysis differentiates multiple system atrophy from Parkinson's disease
2003 · W. Farid Abdo, Daniëlle De Jong, et al. · Movement Disorders · 84
Severity of Parkinson's disease is a risk factor for peak-dose dyskinesia.
1990 · M W Horstink, J C Zijlmans, et al. · Journal of Neurology Neurosurgery & Psychiatry · 75
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Works count: 143
Citation count: 8,611
H-index: 45
I10-index: 92
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