Rakovic A - Search Results

1

α-Synuclein Pathology in PRKN-Linked Parkinson's Disease: New Insights from a Blood-Based Seed Amplification Assay.

Kluge A, Borsche M, Streubel-Gallasch L, Gül T, Schaake S, Balck A, Prasuhn J, Campbell P, Morris HR, Schapira AH, Lohmann K, Brüggemann N, Rakovic A, Seibler P, Başak AN, Berg D, Klein C. Kluge A, et al. Among authors: rakovic a. Ann Neurol. 2024 Jun;95(6):1173-1177. doi: 10.1002/ana.26917. Epub 2024 Mar 28. Ann Neurol. 2024. PMID: 38546204

2

Genetic association study of the P-type ATPase ATP13A2 in late-onset Parkinson's disease.

Rakovic A, Stiller B, Djarmati A, Flaquer A, Freudenberg J, Toliat MR, Linnebank M, Kostic V, Lohmann K, Paus S, Nürnberg P, Kubisch C, Klein C, Wüllner U, Ramirez A. Rakovic A, et al. Mov Disord. 2009 Feb 15;24(3):429-33. doi: 10.1002/mds.22399. Mov Disord. 2009. PMID: 19097176 Free article.

3

Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.

Djarmati A, Schneider SA, Lohmann K, Winkler S, Pawlack H, Hagenah J, Brüggemann N, Zittel S, Fuchs T, Raković A, Schmidt A, Jabusch HC, Wilcox R, Kostić VS, Siebner H, Altenmüller E, Münchau A, Ozelius LJ, Klein C. Djarmati A, et al. Among authors: rakovic a. Lancet Neurol. 2009 May;8(5):447-52. doi: 10.1016/S1474-4422(09)70083-3. Epub 2009 Apr 1. Lancet Neurol. 2009. PMID: 19345148

4

The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?

Brüggemann N, Kock N, Lohmann K, König IR, Rakovic A, Hagenah J, Schmidt A, Ziegler A, Jabusch HC, Siebner H, Altenmüller E, Münchau A, Klein C. Brüggemann N, et al. Among authors: rakovic a. Neurology. 2009 Apr 21;72(16):1441-3. doi: 10.1212/WNL.0b013e3181a1861e. Neurology. 2009. PMID: 19380705 No abstract available.

5

Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients.

Rakovic A, Grünewald A, Seibler P, Ramirez A, Kock N, Orolicki S, Lohmann K, Klein C. Rakovic A, et al. Hum Mol Genet. 2010 Aug 15;19(16):3124-37. doi: 10.1093/hmg/ddq215. Epub 2010 May 27. Hum Mol Genet. 2010. PMID: 20508036

6

Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.

Weissbach A, Djarmati A, Klein C, Dragasević N, Zühlke C, Raković A, Guzvić M, Butz E, Tönnies H, Siebert R, Petrović I, Svetel M, Kostić VS, Lohmann K. Weissbach A, et al. Among authors: rakovic a. Mov Disord. 2010 Aug 15;25(11):1577-82. doi: 10.1002/mds.22857. Mov Disord. 2010. PMID: 20589871

7

Mutant Parkin impairs mitochondrial function and morphology in human fibroblasts.

Grünewald A, Voges L, Rakovic A, Kasten M, Vandebona H, Hemmelmann C, Lohmann K, Orolicki S, Ramirez A, Schapira AH, Pramstaller PP, Sue CM, Klein C. Grünewald A, et al. Among authors: rakovic a. PLoS One. 2010 Sep 27;5(9):e12962. doi: 10.1371/journal.pone.0012962. PLoS One. 2010. PMID: 20885945 Free PMC article.

8

The dystonia gene DYT1 is repressed by the transcription factor THAP1 (DYT6).

Kaiser FJ, Osmanoric A, Rakovic A, Erogullari A, Uflacker N, Braunholz D, Lohnau T, Orolicki S, Albrecht M, Gillessen-Kaesbach G, Klein C, Lohmann K. Kaiser FJ, et al. Among authors: rakovic a. Ann Neurol. 2010 Oct;68(4):554-9. doi: 10.1002/ana.22157. Ann Neurol. 2010. PMID: 20976771

9

Mutations in PINK1 and Parkin impair ubiquitination of Mitofusins in human fibroblasts.

Rakovic A, Grünewald A, Kottwitz J, Brüggemann N, Pramstaller PP, Lohmann K, Klein C. Rakovic A, et al. PLoS One. 2011 Mar 8;6(3):e16746. doi: 10.1371/journal.pone.0016746. PLoS One. 2011. PMID: 21408142 Free PMC article.

10

PINK1-Interacting Proteins: Proteomic Analysis of Overexpressed PINK1.

Rakovic A, Grünewald A, Voges L, Hofmann S, Orolicki S, Lohmann K, Klein C. Rakovic A, et al. Parkinsons Dis. 2011 Mar 16;2011:153979. doi: 10.4061/2011/153979. Parkinsons Dis. 2011. PMID: 21437181 Free PMC article.

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