PuSH - Publication Server of Helmholtz Zentrum München

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1.
Jochim, A.* et al.: Treatment of cervical dystonia with abo- and onabotulinumtoxinA: Long-term safety and efficacy in daily clinical practice. J. Neurol., accepted (2019)
2.
Jochim, A.* et al.: Microstructural white matter abnormalities in patients with COL6A3 mutations (DYT27 dystonia). Parkinsonism Relat. Disord. 46, 74-78 (2018)
3.
Zech, M. et al.: Molecular diversity of combined and complex dystonia: Insights from diagnostic exome sequencing. Neurogenetics 18, 195–205 (2017)
4.
Jochim, A.* ; Zech, M. ; Gora-Stahlberg, G.* ; Winkelmann, J. & Haslinger, B.*: The clinical phenotype of early-onset isolated dystonia caused by recessive COL6A3 mutations (DYT27). Mov. Disord. 31, 747-750 (2016)
5.
Zech, M. et al.: Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls. Parkinsonism Relat. Disord. 31, 119-123 (2016)
6.
Zech, M. et al.: Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up. Mov. Disord. 32, 549-559 (2016)
7.
Zech, M. et al.: Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia. Am. J. Hum. Genet. 96, 883-893 (2015)
8.
Zech, M. et al.: Large-scale TUBB4A mutational screening in isolated dystonia and controls. Parkinsonism Relat. Disord. 21, 1278-1281 (2015)
9.
Zech, M. et al.: Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls. Mov. Disord. 29, 143-147 (2014)
10.
Zech, M. et al.: DYT16 revisited: Exome sequencing identifies PRKRA mutations in a European dystonia family. Mov. Disord. 29, 1504-1510 (2014)
11.
Buck, D.* et al.: Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis. Ann. Neurol. 73, 86-94 (2013)
12.
International Multiple Sclerosis Genetics Consortium (Illig, T. ; Lichtner, P.) et al.: Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat. Genet. 45, 1353-1360 (2013)
13.
Schulte, E.C. et al.: Mitochondrial membrane protein associated neurodegeneration: A novel variant of neurodegeneration with brain iron accumulation. Mov. Disord. 28, 224-227 (2013)
14.
Zech, M. et al.: Niemann-pick C disease gene mutations and age-related neurodegenerative disorders. PLoS ONE 8:e82879 (2013)