Armin Giese
Armin Giese
Professor for Neuropathology, Ludwig-Maximilians-Universität München; CSO MODAG GmbH
Verified email at modag.net - Homepage
Title
Cited by
Cited by
Year
The cellular prion protein binds copper in vivo
DR Brown, K Qin, JW Herms, A Madlung, J Manson, R Strome, PE Fraser, ...
Nature 390 (18/25), 685, 1997
14971997
Classification of sporadic Creutzfeldt‐Jakob disease based on molecular and phenotypic analysis of 300 subjects
P Parchi, A Giese, S Capellari, P Brown, W Schulz‐Schaeffer, O Windl, ...
Annals of neurology 46 (2), 224-233, 1999
13241999
Different species of α-synuclein oligomers induce calcium influx and seeding
KM Danzer, D Haasen, AR Karow, S Moussaud, M Habeck, A Giese, ...
Journal of Neuroscience 27 (34), 9220-9232, 2007
6902007
Clinical diagnosis of progressive supranuclear palsy: the movement disorder society criteria
GU Höglinger, G Respondek, M Stamelou, C Kurz, KA Josephs, AE Lang, ...
Movement Disorders 32 (6), 853-864, 2017
5422017
Prevalence of superficial siderosis in patients with cerebral amyloid angiopathy
J Linn, A Halpin, P Demaerel, J Ruhland, AD Giese, M Dichgans, ...
Neurology 74 (17), 1346-1350, 2010
5342010
Inhibition of mitochondrial fusion by α-synuclein is rescued by PINK1, Parkin and DJ-1
F Kamp, N Exner, AK Lutz, N Wender, J Hegermann, B Brunner, ...
The EMBO journal 29 (20), 3571-3589, 2010
4532010
Evidence of presynaptic location and function of the prion protein
J Herms, T Tings, S Gall, A Madlung, A Giese, H Siebert, P Schürmann, ...
Journal of Neuroscience 19 (20), 8866-8875, 1999
4031999
Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets
J Bieschke, A Giese, W Schulz-Schaeffer, I Zerr, S Poser, M Eigen, ...
Proceedings of the National Academy of Sciences 97 (10), 5468-5473, 2000
3062000
Chaperonin TRiC promotes the assembly of polyQ expansion proteins into nontoxic oligomers
C Behrends, CA Langer, R Boteva, UM Böttcher, MJ Stemp, G Schaffar, ...
Molecular cell 23 (6), 887-897, 2006
2942006
Typing prion isoforms
P Parchi, S Capellari, SG Chen, RB Petersen, P Gambetti, N Kopp, ...
Nature 386, 232-233, 1997
2811997
Role of microglia in neuronal cell death in prion disease
A Giese, DR Brown, MH Groschup, C Feldmann, I Haist, HA Kretzschmar
Brain pathology 8 (3), 449-457, 1998
2711998
The Paraffin-Embedded Tissue Blot Detects PrPSc Early in the Incubation Time in Prion Diseases
WJ Schulz-Schaeffer, S Tschöke, N Kranefuss, W Dröse, D Hause-Reitner, ...
The American journal of pathology 156 (1), 51-56, 2000
2362000
Single particle characterization of iron-induced pore-forming α-synuclein oligomers
M Kostka, T Högen, KM Danzer, J Levin, M Habeck, A Wirth, R Wagner, ...
Journal of Biological Chemistry 283 (16), 10992-11003, 2008
2352008
Anle138b: a novel oligomer modulator for disease-modifying therapy of neurodegenerative diseases such as prion and Parkinson’s disease
J Wagner, S Ryazanov, A Leonov, J Levin, S Shi, F Schmidt, C Prix, ...
Acta neuropathologica 125 (6), 795-813, 2013
2242013
Current clinical diagnosis in Creutzfeldt‐Jakob disease: Identification of uncommon variants
I Zerr, WJ Schulz‐Schaeffer, A Giese, M Bodemer, A Schröter, K Henkel, ...
Annals of neurology 48 (3), 323-329, 2000
2192000
Molecular genetics of human prion diseases in Germany
O Windl, A Giese, W Schulz-Schaeffer, I Zerr, K Skworc, S Arendt, ...
Human genetics 105 (3), 244-252, 1999
2191999
Quantifying prion disease penetrance using large population control cohorts
EV Minikel, SM Vallabh, M Lek, K Estrada, KE Samocha, ...
Science Translational Medicine 8 (322), 322ra9-322ra9, 2016
2092016
Case-control study of risk factors of Creutzfeldt-Jakob disease in Europe during 1993--95
CM Van Duijn, N Delasnerie-Laupretre, C Masullo, I Zerr, R Silva, ...
Lancet 351, 1081-5, 1998
2051998
The phenotypic spectrum of progressive supranuclear palsy: a retrospective multicenter study of 100 definite cases
G Respondek, M Stamelou, C Kurz, LW Ferguson, A Rajput, WZ Chiu, ...
Movement disorders 29 (14), 1758-1766, 2014
1982014
Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrP Sc types: an updated classification
P Parchi, R Strammiello, S Notari, A Giese, JPM Langeveld, A Ladogana, ...
Acta neuropathologica 118 (5), 659-671, 2009
1972009
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