Articles with public access mandates - Durr AlexandraLearn more
Not available anywhere: 8
Myoclonus–dystonia: Clinical and electrophysiologic pattern related to SGCE mutations
E Roze, E Apartis, F Clot, N Dorison, S Thobois, L Guyant-Marechal, ...
Neurology 70 (13), 1010-1016, 2008
Mandates: National Institute of Health and Medical Research, France
PRRT2 mutations: A major cause of paroxysmal kinesigenic dyskinesia in the European population
A Méneret, D Grabli, C Depienne, C Gaudebout, F Picard, A Dürr, ...
Neurology 79 (2), 170-174, 2012
Mandates: Swiss National Science Foundation, Research Foundation (Flanders), National …
Self‐rated health status in spinocerebellar ataxia—Results from a European multicenter study
T Schmitz‐Hübsch, M Coudert, P Giunti, C Globas, L Baliko, R Fancellu, ...
Movement disorders 25 (5), 587-595, 2010
Mandates: German Research Foundation, Hungarian Scientific Research Fund
Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls
S Lesage, E Lohmann, F Tison, F Durif, A Dürr, A Brice, ...
Journal of medical genetics 45 (1), 43-46, 2008
Mandates: National Institute of Health and Medical Research, France
Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians
K Ishikawa, A Dürr, T Klopstock, S Müller, B De Toffol, M Vidailhet, ...
Neurology 77 (20), 1853-1855, 2011
Mandates: German Research Foundation
Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa
S Lesage, C Condroyer, N Hecham, M Anheim, S Belarbi, E Lohman, ...
Neurology 76 (3), 301-303, 2011
Mandates: Research Foundation (Flanders), National Institute of Health and Medical …
Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24
R Schule, M Bonin, A Durr, S Forlani, AD Sperfeld, S Klimpe, JC Mueller, ...
Neurology 72 (22), 1893-1898, 2009
Mandates: German Research Foundation
Low disease risk in relatives of north african lrrk2 Parkinson disease patients
AR Troiano, A Elbaz, E Lohmann, S Belarbi, M Vidailhet, AM Bonnet, ...
Neurology 75 (12), 1118-1119, 2010
Mandates: National Institute of Health and Medical Research, France
Available somewhere: 43
Second consensus statement on the diagnosis of multiple system atrophy
S Gilman, GK Wenning, PA Low, DJ Brooks, CJ Mathias, JQ Trojanowski, ...
Neurology 71 (9), 670-676, 2008
Mandates: US National Institutes of Health
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
E Sidransky, MA Nalls, JO Aasly, J Aharon-Peretz, G Annesi, ER Barbosa, ...
New England Journal of Medicine 361 (17), 1651-1661, 2009
Mandates: US National Institutes of Health
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
Mandates: US National Institutes of Health, UK Economic and Social Research Council …
Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt, M Jacoupy, A Nicolas, ...
The American Journal of Human Genetics 98 (3), 500-513, 2016
Mandates: US National Institutes of Health, National Institute of Health and Medical …
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
LA Robak, IE Jansen, J Van Rooij, AG Uitterlinden, R Kraaij, J Jankovic, ...
Brain 140 (12), 3191-3203, 2017
Mandates: US Department of Defense, US National Institutes of Health, Helmholtz …
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
Mandates: US National Institutes of Health, Motor Neurone Disease Association, UK, UK …
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
A Beilina, IN Rudenko, A Kaganovich, L Civiero, H Chau, SK Kalia, ...
Proceedings of the National Academy of Sciences 111 (7), 2626-2631, 2014
Mandates: US National Institutes of Health, Research Foundation (Flanders), Fondazione …
Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy
Multiple-System Atrophy Research Collaboration
New England Journal of Medicine 369 (3), 233-244, 2013
Mandates: US National Institutes of Health, German Research Foundation
Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease
C Lautier, S Goldwurm, A Dürr, B Giovannone, WG Tsiaras, G Pezzoli, ...
The American Journal of Human Genetics 82 (4), 822-833, 2008
Mandates: US National Institutes of Health
The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study
H Jacobi, P Bauer, P Giunti, R Labrum, MG Sweeney, P Charles, A Duerr, ...
Neurology 77 (11), 1035-1041, 2011
Mandates: German Research Foundation, Hungarian Scientific Research Fund, Government …
A two-stage meta-analysis identifies several new loci for Parkinson's disease
International Parkinson's Disease Genomics Consortium (IPDGC), ...
PLoS genetics 7 (6), e1002142, 2011
Mandates: US National Institutes of Health, Parkinson's UK
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6
JB Schulz, J Borkert, S Wolf, T Schmitz-Hübsch, M Rakowicz, C Mariotti, ...
Neuroimage 49 (1), 158-168, 2010
Mandates: German Research Foundation
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