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

2

Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.

Hiller A, Hagenah JM, Djarmati A, Hedrich K, Reetz K, Schneider-Gold C, Kress W, Münchau A, Klein C. Hiller A, et al. Among authors: reetz k. Mov Disord. 2007 Jan;22(1):145-7. doi: 10.1002/mds.21059. Mov Disord. 2007. PMID: 17013904

3

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.

4

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

5

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

6

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

7

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.

8

Premotor Gray Matter Volume is Associated with Clinical Findings in Idiopathic and Genetically Determined Parkinson's Disease.

Reetz K, Siebner HR, Gaser C, Hagenah J, Buechel C, Kasten M, Petersen D, Pramstaller PP, Klein C, Binkofksi F. Reetz K, et al. Open Neuroimag J. 2008 Sep 27;2:102-5. doi: 10.2174/1874440000802010102. Open Neuroimag J. 2008. PMID: 19526072 Free PMC article.

9

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

10

Digitized spiral analysis is a promising early motor marker for Parkinson Disease.

Stanley K, Hagenah J, Brüggemann N, Reetz K, Severt L, Klein C, Yu Q, Derby C, Pullman S, Saunders-Pullman R. Stanley K, et al. Among authors: reetz k. Parkinsonism Relat Disord. 2010 Mar;16(3):233-4. doi: 10.1016/j.parkreldis.2009.12.007. Epub 2010 Jan 15. Parkinsonism Relat Disord. 2010. PMID: 20079674 Free PMC article. No abstract available.

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