Kathrin Reetz
Kathrin Reetz
Dep. of Neurology, RWTH Aachen University; JARA BRAIN
Bestätigte E-Mail-Adresse bei ukaachen.de
Titel
Zitiert von
Zitiert von
Jahr
Modelling neural correlates of working memory: a coordinate-based meta-analysis
C Rottschy, R Langner, I Dogan, K Reetz, AR Laird, JB Schulz, PT Fox, ...
Neuroimage 60 (1), 830-846, 2012
5542012
No double-dissociation between optic ataxia and visual agnosia: Multiple sub-streams for multiple visuo-manual integrations
L Pisella, F Binkofski, K Lasek, I Toni, Y Rossetti
Neuropsychologia 44 (13), 2734-2748, 2006
2112006
Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?
K Hedrich, J Hagenah, A Djarmati, A Hiller, T Lohnau, K Lasek, ...
Archives of neurology 63 (6), 833-838, 2006
1302006
The Montreal Cognitive Assessment (MoCA)-a sensitive screening instrument for detecting cognitive impairment in chronic hemodialysis patients
FE Tiffin-Richards, AS Costa, B Holschbach, RD Frank, A Vassiliadou, ...
PloS one 9 (10), 2014
1062014
Multisensory integration mechanisms during aging
J Freiherr, JN Lundström, U Habel, K Reetz
Frontiers in human neuroscience 7, 863, 2013
1022013
Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data
H Jacobi, K Reetz, ST du Montcel, P Bauer, C Mariotti, L Nanetti, ...
The Lancet Neurology 12 (7), 650-658, 2013
1012013
Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data
K Reetz, I Dogan, AS Costa, M Dafotakis, K Fedosov, P Giunti, ...
The Lancet Neurology 14 (2), 174-182, 2015
1002015
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
DJH Moss, AF Pardiñas, D Langbehn, K Lo, BR Leavitt, R Roos, A Durr, ...
The Lancet Neurology 16 (9), 701-711, 2017
912017
Alternate-form reliability of the Montreal cognitive assessment screening test in a clinical setting
AS Costa, B Fimm, P Friesen, H Soundjock, C Rottschy, T Gross, F Eitner, ...
Dementia and geriatric cognitive disorders 33 (6), 379-384, 2012
832012
Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)
K Lasek, R Lencer, C Gaser, J Hagenah, U Walter, A Wolters, N Kock, ...
Brain 129 (9), 2341-2352, 2006
812006
Loss of annexin A7 leads to alterations in frequency-induced shortening of isolated murine cardiomyocytes
C Herr, N Smyth, S Ullrich, F Yun, P Sasse, J Hescheler, B Fleischmann, ...
Molecular and cellular biology 21 (13), 4119-4128, 2001
812001
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6
K Reetz, AS Costa, S Mirzazade, A Lehmann, A Juzek, M Rakowicz, ...
Brain 136 (3), 905-917, 2013
752013
Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia
F Binkofski, K Reetz, C Gaser, R Hilker, J Hagenah, K Hedrich, ...
Neurology 69 (9), 842-850, 2007
742007
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype
N Brüggemann, J Hagenah, K Reetz, A Schmidt, M Kasten, I Buchmann, ...
Archives of neurology 67 (11), 1357-1363, 2010
732010
Altered resting‐state connectivity in Huntington's disease
CJ Werner, I Dogan, C Saß, S Mirzazade, J Schiefer, NJ Shah, JB Schulz, ...
Human brain mapping 35 (6), 2582-2593, 2014
692014
Differentiated parietal connectivity of frontal regions for “what” and “where” memory
C Rottschy, S Caspers, C Roski, K Reetz, I Dogan, JB Schulz, K Zilles, ...
Brain Structure and function 218 (6), 1551-1567, 2013
652013
Investigating function and connectivity of morphometric findings—exemplified on cerebellar atrophy in spinocerebellar ataxia 17 (SCA17)
K Reetz, I Dogan, A Rolfs, F Binkofski, JB Schulz, AR Laird, PT Fox, ...
Neuroimage 62 (3), 1354-1366, 2012
632012
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype
BFL Van Nuenen, MM Weiss, BR Bloem, K Reetz, T Van Eimeren, ...
Neurology 72 (12), 1041-1047, 2009
622009
ATP13A2 variants in early‐onset Parkinson's disease patients and controls
A Djarmati, J Hagenah, K Reetz, S Winkler, MI Behrens, H Pawlack, ...
Movement disorders: official journal of the Movement Disorder Society 24 (14 …, 2009
602009
Early Parkinson's disease: longitudinal changes in brain activity during sequence learning
M Carbon, K Reetz, MF Ghilardi, V Dhawan, D Eidelberg
Neurobiology of disease 37 (2), 455-460, 2010
582010
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