Prof. Dr. Rejko Krüger, MD
Prof. Dr. Rejko Krüger, MD
Luxembourg Institute of Health and University of Luxembourg
Verified email at - Homepage
Cited by
Cited by
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
Ala30Pro mutation in the gene encoding α-synuclein in Parkinson's disease
R Krüger, W Kuhn, T Müller, D Woitalla, M Graeber, S Kösel, H Przuntek, ...
Nature genetics 18 (2), 106-108, 1998
Genome-wide association study reveals genetic risk underlying Parkinson's disease
J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ...
Nature genetics 41 (12), 1308-1312, 2009
Neurostimulation for Parkinson's disease with early motor complications
WMM Schuepbach, J Rau, K Knudsen, J Volkmann, P Krack, ...
New England Journal of Medicine 368 (7), 610-622, 2013
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease
KM Strauss, LM Martins, H Plun-Favreau, FP Marx, S Kautzmann, D Berg, ...
Human molecular genetics 14 (15), 2099-2111, 2005
Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease
LF Burbulla, P Song, JR Mazzulli, E Zampese, YC Wong, S Jeon, ...
Science 357 (6357), 1255-1261, 2017
Loss-of-function of human PINK1 results in mitochondrial pathology and can be rescued by parkin
N Exner, B Treske, D Paquet, K Holmström, C Schiesling, S Gispert, ...
Journal of Neuroscience 27 (45), 12413-12418, 2007
Collaborative analysis of α-synuclein gene promoter variability and Parkinson disease
DM Maraganore, M De Andrade, A Elbaz, MJ Farrer, JP Ioannidis, ...
Jama 296 (6), 661-670, 2006
Genetic correction of a LRRK2 mutation in human iPSCs links parkinsonian neurodegeneration to ERK-dependent changes in gene expression
P Reinhardt, B Schmid, LF Burbulla, DC Schöndorf, L Wagner, M Glatza, ...
Cell stem cell 12 (3), 354-367, 2013
Reduced basal autophagy and impaired mitochondrial dynamics due to loss of Parkinson's disease-associated protein DJ-1
G Krebiehl, S Ruckerbauer, LF Burbulla, N Kieper, B Maurer, J Waak, ...
PloS one 5 (2), e9367, 2010
The hallmarks of P arkinson's disease
PMA Antony, NJ Diederich, R Krüger, R Balling
The FEBS journal 280 (23), 5981-5993, 2013
Increased susceptibility to sporadic Parkinson's disease by a certain combined α‐synuclein/apolipoprotein E genotype
R Krüger, AM Menezes Vieira‐Saecker, W Kuhn, D Berg, T Müller, ...
Annals of Neurology: Official Journal of the American Neurological …, 1999
UCHL1 is a Parkinson's disease susceptibility gene
DM Maraganore, TG Lesnick, A Elbaz, MC Chartier‐Harlin, T Gasser, ...
Annals of neurology 55 (4), 512-521, 2004
The brainstem pathologies of Parkinson's disease and dementia with Lewy bodies
K Seidel, J Mahlke, S Siswanto, R Krüger, H Heinsen, G Auburger, ...
Brain pathology 25 (2), 121-135, 2015
Nigral stimulation for resistant axial motor impairment in Parkinson’s disease? A randomized controlled trial
D Weiss, M Walach, C Meisner, M Fritz, M Scholten, S Breit, C Plewnia, ...
Brain 136 (7), 2098-2108, 2013
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
R Chia, MS Sabir, S Bandres-Ciga, S Saez-Atienzar, RH Reynolds, ...
Nature genetics 53 (3), 294-303, 2021
Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds
L Schöls, R Krüger, G Amoiridis, H Przuntek, JT Epplen, O Riess
Journal of Neurology, Neurosurgery & Psychiatry 64 (1), 67-73, 1998
Familial Parkinson's disease–genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease
C Schiesling, N Kieper, K Seidel, R Krüger
Neuropathology and applied neurobiology 34 (3), 255-271, 2008
Mitochondrial protein quality control by the proteasome involves ubiquitination and the protease Omi
S Radke, H Chander, P Schäfer, G Meiss, R Krüger, JB Schulz, ...
Journal of Biological Chemistry 283 (19), 12681-12685, 2008
Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers
R Kruger, W Kuhn, KL Leenders, R Sprengelmeyer, T Muller, D Woitalla, ...
Neurology 56 (10), 1355-1362, 2001
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