PuSH - Publikationsserver des Helmholtz Zentrums München

9 Datensätze gefunden.
Zum Exportieren der Ergebnisse bitte einloggen.
Alle Publikationen dieser Seite in den Korb legen
1.
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., DOI: 10.1111/ene.14952 (2021)
2.
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)
3.
Krenn, M.* et al.: Clinical whole-exome sequencing for the diagnosis of Mendelian neuromuscular disorders. Eur. J. Neurol. 25, 2, 549-549 (2018)
4.
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)
5.
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)
6.
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)
7.
Bluher, A.* et al.: Heritability of young- and old-onset ischaemic stroke. Eur. J. Neurol. 22, 1488-1491 (2015)
8.
Kuepper, C.* et al.: Familial dyskinesia with facial myokymia due to ADCY5 mutation: Treatment with propranolol. Eur. J. Neurol. 22, 30 (2015)
9.
Bigalke, B.* et al.: Expression of platelet glycoprotein VI is associated with transient ischemic attack and stroke. Eur. J. Neurol. 17, 111-117 (2009)