Reetz K - Search Results

1

Investigating function and connectivity of morphometric findings--exemplified on cerebellar atrophy in spinocerebellar ataxia 17 (SCA17).

Reetz K, Dogan I, Rolfs A, Binkofski F, Schulz JB, Laird AR, Fox PT, Eickhoff SB. Reetz K, et al. Neuroimage. 2012 Sep;62(3):1354-66. doi: 10.1016/j.neuroimage.2012.05.058. Epub 2012 May 30. Neuroimage. 2012. PMID: 22659444 Free PMC article.

2

Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.

Hagenah J, Reetz K, Zühlke C, Rolfs A, Binkofski F, Klein C. Hagenah J, et al. Among authors: reetz k. Neurology. 2007 Jun 12;68(24):2157; author reply 2157-8. doi: 10.1212/01.wnl.0000269478.69285.7e. Neurology. 2007. PMID: 17562842 No abstract available.

3

Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia.

Binkofski F, Reetz K, Gaser C, Hilker R, Hagenah J, Hedrich K, van Eimeren T, Thiel A, Büchel C, Pramstaller PP, Siebner HR, Klein C. Binkofski F, et al. Among authors: reetz k. Neurology. 2007 Aug 28;69(9):842-50. doi: 10.1212/01.wnl.0000267844.72421.6c. Neurology. 2007. PMID: 17724286

4

Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers.

Reetz K, Lencer R, Steinlechner S, Gaser C, Hagenah J, Büchel C, Petersen D, Kock N, Djarmati A, Siebner HR, Klein C, Binkofski F. Reetz K, et al. Biol Psychiatry. 2008 Aug 1;64(3):241-7. doi: 10.1016/j.biopsych.2007.12.010. Epub 2008 Feb 7. Biol Psychiatry. 2008. PMID: 18261714

5

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. Mov Disord. 2009 Jan 15;24(1):99-103. doi: 10.1002/mds.22333. Mov Disord. 2009. PMID: 18823048

6

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: reetz k. 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.

7

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: reetz k. Mov Disord. 2009 Oct 30;24(14):2104-11. doi: 10.1002/mds.22728. Mov Disord. 2009. PMID: 19705361

8

Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17.

Reetz K, Lencer R, Hagenah JM, Gaser C, Tadic V, Walter U, Wolters A, Steinlechner S, Zühlke C, Brockmann K, Klein C, Rolfs A, Binkofski F. Reetz K, et al. Cerebellum. 2010 Jun;9(2):210-7. doi: 10.1007/s12311-009-0150-4. Cerebellum. 2010. PMID: 20016963

9

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. 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

10

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. Among authors: reetz k. Arch Neurol. 2010 Nov;67(11):1357-63. doi: 10.1001/archneurol.2010.281. Arch Neurol. 2010. PMID: 21060012

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