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Grover, S.* et al.: Genome-wide association and meta-analysis of age-at-onset in parkinson disease: Evidence from COURAGE-PD consortium. Neurology 99, e698-e710 (2022)
Jaworek, T.* et al.: Contribution of common genetic variants to risk of early onset ischemic stroke. Neurology 99, E1738-E1754 (2022)
Papadopoulos, A.* et al.: Circulating interleukin-6 levels and incident ischemic stroke: A systematic review and meta-analysis of prospective studies Neurology 98, e1002-e1012 (2022)
Lo, C.* et al.: Olfactory testing in Parkinson's Disease & REM behavior disorder: A machine learning approach. Neurology 96, e2016-e2027 (2021)
Baumeister, S. et al.: Physical activity and risk of Alzheimer disease A 2-sample mendelian randomization study. Neurology 95, E1897-E1905 (2020)
Bernath, M.M.* et al.: Serum triglycerides in Alzheimer disease: Relation to neuroimaging and CSF biomarkers. Neurology 94, E2088-E2098 (2020)
Senderek, J.* et al.: The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME. Neurology 95, e3163-e3179 (2020)
Chauhan, G.* et al.: Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. Neurology 92, e486-e503 (2019)
Larsson, S.C.* et al.: Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study. Neurology 92, e944-e950 (2019)
Valdes-Marquez, E.* et al.: Relative effects of LDL-C on ischemic stroke and coronary disease: A Mendelian randomization study. Neurology 92, E1176-E1187 (2019)
Rannikme, K.* et al.: COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology 89, 1829-1839 (2017)
la Piana, R.* et al.: Diffuse hypomyelination is not obligate for POLR3-related disorders. Neurology 86, 1622-1626 (2016)
Malik, R.* et al.: Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology 86, 1217-1226 (2016)
Trenkwalder, C.* ; Allen, R.P.* ; Högl, B.* ; Paulus, W.* & Winkelmann, J.: Restless legs syndrome associated with major diseases: A systematic review and new concept. Neurology 86, 1336-1343 (2016)
Wang, L.* et al.: Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. Neurology 85, 1283-1292 (2015)
Dallabona, C.* et al.: Novel (ovario) leukodystrophy related to AARS2 mutations. Neurology 82, 2063-2071 (2014)
Gess, B.* et al.: HSJ1-related hereditary neuropathies: Novel mutations and extended clinical spectrum. Neurology 83, 1726-1732 (2014)
Schirmer, L.* et al.: Differential Loss of KIR4.1 on Oligodendrocytes and Astrocytes in Multiple Sclerosis Lesions. Neurology 80 (2013)
Sharma, M.L.* et al.: Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology 79, 659-667 (2012)
Ishikawa, K.* et al.: Pentanucleotide repeats at the spinocerebellar ataxia type 31 (SCA31) locus in Caucasians. Neurology 77, 1853-1855 (2011)