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1.
Ahn, N.* et al.: Emulating a target trial of proton pump inhibitors and dementia risk using claims data. Eur. J. Neurol. 29, 1335-1343 (2022)
2.
Kender, Z.* et al.: Diabetic neuropathy is a generalized phenomenon with impact on hand functional performance and quality of life. Eur. J. Neurol. 29, 3081-3091 (2022)
3.
Krenn, M.* et al.: Clinico-genetic spectrum of limb-girdle muscular weakness in Austria: A multi-centre cohort study. Eur. J. Neurol. 29, 1815-1824 (2022)
4.
Schulte, E.C. ; Hauer, L.* ; Kunz, A.B.* & Sellner, J.*: Systematic review of cases of acute myelitis in individuals with COVID-19. Eur. J. Neurol. 28, 3230-3244 (2021)
5.
Krenn, M.* et al.: Genotype-guided diagnostic reassessment after exome sequencing in neuromuscular disorders: Experiences with a two-step approach. Eur. J. Neurol. 27, 51-61 (2020)
6.
Krenn, M.* et al.: Clinical whole-exome sequencing for the diagnosis of Mendelian neuromuscular disorders. Eur. J. Neurol. 25, 2, 549-549 (2018)
7.
Tan, J.* et al.: Estimated lifetime prevalences of autosomal mitochondrial disorders based on allele frequencies of pathogenic variants in exome databases. Eur. J. Neurol. 25, 31-31 (2018)
8.
Kaminski, M.* ; Grummel, V.* ; Hoffmann, D. ; Berthele, A.* & Hemmer, B.*: The spectrum of aseptic central nervous system infections in southern Germany - demographic, clinical and laboratory findings. Eur. J. Neurol. 24, 1062-1070 (2017)
9.
Krenn, M.* et al.: Hereditary spastic paraplegia caused by compound heterozygous mutations outside the motor domain of the KIF1A gene. Eur. J. Neurol. 24, 741-747 (2017)
10.
Bluher, A.* et al.: Heritability of young- and old-onset ischaemic stroke. Eur. J. Neurol. 22, 1488-1491 (2015)
11.
Kuepper, C.* et al.: Familial dyskinesia with facial myokymia due to ADCY5 mutation: Treatment with propranolol. Eur. J. Neurol. 22, 30 (2015)
12.
Bigalke, B.* et al.: Expression of platelet glycoprotein VI is associated with transient ischemic attack and stroke. Eur. J. Neurol. 17, 111-117 (2009)
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