Siebner HR - Search Results

1

ATP13A2 variants in early-onset Parkinson's disease patients and controls.

Djarmati A, Hagenah J, Reetz K, Winkler S, Behrens MI, Pawlack H, Lohmann K, Ramirez A, Tadić V, Brüggemann N, Berg D, Siebner HR, Lang AE, Pramstaller PP, Binkofski F, Kostić VS, Volkmann J, Gasser T, Klein C. Djarmati A, et al. Among authors: siebner hr. Mov Disord. 2009 Oct 30;24(14):2104-11. doi: 10.1002/mds.22728. Mov Disord. 2009. PMID: 19705361

2

Structural findings in the basal ganglia in genetically determined and idiopathic Parkinson's disease.

Reetz K, Gaser C, Klein C, Hagenah J, Büchel C, Gottschalk S, Pramstaller PP, Siebner HR, Binkofski F. Reetz K, et al. Among authors: siebner hr. Mov Disord. 2009 Jan 15;24(1):99-103. doi: 10.1002/mds.22333. Mov Disord. 2009. PMID: 18823048

3

Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease.

Kertelge L, Brüggemann N, Schmidt A, Tadic V, Wisse C, Dankert S, Drude L, van der Vegt J, Siebner H, Pawlack H, Pramstaller PP, Behrens MI, Ramirez A, Reichel D, Buhmann C, Hagenah J, Klein C, Lohmann K, Kasten M. Kertelge L, et al. Mov Disord. 2010 Nov 15;25(15):2665-9. doi: 10.1002/mds.23272. Mov Disord. 2010. PMID: 20721915

4

Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.

Brüggemann N, Hagenah J, Reetz K, Schmidt A, Kasten M, Buchmann I, Eckerle S, Bähre M, Münchau A, Djarmati A, van der Vegt J, Siebner H, Binkofski F, Ramirez A, Behrens MI, Klein C. Brüggemann N, et al. Arch Neurol. 2010 Nov;67(11):1357-63. doi: 10.1001/archneurol.2010.281. Arch Neurol. 2010. PMID: 21060012

5

Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease.

Kasten M, Kertelge L, Tadic V, Brüggemann N, Schmidt A, van der Vegt J, Siebner H, Buhmann C, Lencer R, Kumar KR, Lohmann K, Hagenah J, Klein C. Kasten M, et al. Mov Disord. 2012 May;27(6):754-9. doi: 10.1002/mds.24999. Epub 2012 May 1. Mov Disord. 2012. PMID: 22550041

6

Responsiveness to distracting stimuli, though increased in Parkinson's disease, is decreased in asymptomatic PINK1 and Parkin mutation carriers.

Verleger R, Hagenah J, Weiss M, Ewers T, Heberlein I, Pramstaller PP, Siebner HR, Klein C. Verleger R, et al. Among authors: siebner hr. Neuropsychologia. 2010 Jan;48(2):467-76. doi: 10.1016/j.neuropsychologia.2009.10.004. Epub 2009 Oct 12. Neuropsychologia. 2010. PMID: 19822161

7

Mapping preclinical compensation in Parkinson's disease: an imaging genomics approach.

van Nuenen BF, van Eimeren T, van der Vegt JP, Buhmann C, Klein C, Bloem BR, Siebner HR. van Nuenen BF, et al. Among authors: siebner hr. Mov Disord. 2009;24 Suppl 2:S703-10. doi: 10.1002/mds.22635. Mov Disord. 2009. PMID: 19877238 Review.

8

Structural imaging in the presymptomatic stage of genetically determined parkinsonism.

Reetz K, Tadic V, Kasten M, Brüggemann N, Schmidt A, Hagenah J, Pramstaller PP, Ramirez A, Behrens MI, Siebner HR, Klein C, Binkofski F. Reetz K, et al. Among authors: siebner hr. Neurobiol Dis. 2010 Sep;39(3):402-8. doi: 10.1016/j.nbd.2010.05.006. Epub 2010 May 17. Neurobiol Dis. 2010. PMID: 20483373

9

Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.

van Nuenen BF, Weiss MM, Bloem BR, Reetz K, van Eimeren T, Lohmann K, Hagenah J, Pramstaller PP, Binkofski F, Klein C, Siebner HR. van Nuenen BF, et al. Among authors: siebner hr. Neurology. 2009 Mar 24;72(12):1041-7. doi: 10.1212/01.wnl.0000338699.56379.11. Epub 2008 Nov 26. Neurology. 2009. PMID: 19038850 Free PMC article.

10

Imaging the impact of genes on Parkinson's disease.

van der Vegt JP, van Nuenen BF, Bloem BR, Klein C, Siebner HR. van der Vegt JP, et al. Among authors: siebner hr. Neuroscience. 2009 Nov 24;164(1):191-204. doi: 10.1016/j.neuroscience.2009.01.055. Epub 2009 Feb 3. Neuroscience. 2009. PMID: 19409223 Review.

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