Zech M - Search Results

1

Dystonia in ATP Synthase Defects: Reconnecting Mitochondria and Dopamine.

Indelicato E, Boesch S, Mencacci NE, Ghezzi D, Prokisch H, Winkelmann J, Zech M. Indelicato E, et al. Among authors: zech m. Mov Disord. 2024 Jan;39(1):29-35. doi: 10.1002/mds.29657. Epub 2023 Nov 14. Mov Disord. 2024. PMID: 37964479 Free article. No abstract available.

2

Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls.

Zech M, Gross N, Jochim A, Castrop F, Kaffe M, Dresel C, Lichtner P, Peters A, Gieger C, Meitinger T, Haslinger B, Winkelmann J. Zech M, et al. Mov Disord. 2014 Jan;29(1):143-7. doi: 10.1002/mds.25715. Epub 2013 Oct 22. Mov Disord. 2014. PMID: 24151159

3

Niemann-Pick C disease gene mutations and age-related neurodegenerative disorders.

Zech M, Nübling G, Castrop F, Jochim A, Schulte EC, Mollenhauer B, Lichtner P, Peters A, Gieger C, Marquardt T, Vanier MT, Latour P, Klünemann H, Trenkwalder C, Diehl-Schmid J, Perneczky R, Meitinger T, Oexle K, Haslinger B, Lorenzl S, Winkelmann J. Zech M, et al. PLoS One. 2013 Dec 30;8(12):e82879. doi: 10.1371/journal.pone.0082879. eCollection 2013. PLoS One. 2013. PMID: 24386122 Free PMC article.

4

DYT16 revisited: exome sequencing identifies PRKRA mutations in a European dystonia family.

Zech M, Castrop F, Schormair B, Jochim A, Wieland T, Gross N, Lichtner P, Peters A, Gieger C, Meitinger T, Strom TM, Oexle K, Haslinger B, Winkelmann J. Zech M, et al. Mov Disord. 2014 Oct;29(12):1504-10. doi: 10.1002/mds.25981. Epub 2014 Aug 20. Mov Disord. 2014. PMID: 25142429

5

Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.

Zech M, Castrop F, Haslinger B, Winkelmann J. Zech M, et al. Mov Disord. 2015 May;30(6):878-9. doi: 10.1002/mds.26233. Epub 2015 Apr 25. Mov Disord. 2015. PMID: 25914261 No abstract available.

6

Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia.

Zech M, Lam DD, Francescatto L, Schormair B, Salminen AV, Jochim A, Wieland T, Lichtner P, Peters A, Gieger C, Lochmüller H, Strom TM, Haslinger B, Katsanis N, Winkelmann J. Zech M, et al. Am J Hum Genet. 2015 Jun 4;96(6):883-93. doi: 10.1016/j.ajhg.2015.04.010. Epub 2015 May 21. Am J Hum Genet. 2015. PMID: 26004199 Free PMC article.

7

Large-scale TUBB4A mutational screening in isolated dystonia and controls.

Zech M, Boesch S, Jochim A, Graf S, Lichtner P, Peters A, Gieger C, Mueller J, Poewe W, Haslinger B, Winkelmann J. Zech M, et al. Parkinsonism Relat Disord. 2015 Oct;21(10):1278-81. doi: 10.1016/j.parkreldis.2015.08.017. Epub 2015 Aug 20. Parkinsonism Relat Disord. 2015. PMID: 26318963

8

TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia.

Zech M, Boesch S, Sycha T, Mueller J, Poewe W, Winkelmann J. Zech M, et al. Mov Disord. 2015 Nov;30(13):1853-4. doi: 10.1002/mds.26458. Epub 2015 Oct 28. Mov Disord. 2015. PMID: 26506956 No abstract available.

9

The clinical phenotype of early-onset isolated dystonia caused by recessive COL6A3 mutations (DYT27).

Jochim A, Zech M, Gora-Stahlberg G, Winkelmann J, Haslinger B. Jochim A, et al. Among authors: zech m. Mov Disord. 2016 May;31(5):747-50. doi: 10.1002/mds.26501. Epub 2015 Dec 21. Mov Disord. 2016. PMID: 26687111

10

Systematic TOR1A non-c.907_909delGAG variant analysis in isolated dystonia and controls.

Zech M, Jochim A, Boesch S, Weber S, Meindl T, Peters A, Gieger C, Mueller J, Messner M, Ceballos-Baumann A, Poewe W, Haslinger B, Winkelmann J. Zech M, et al. Parkinsonism Relat Disord. 2016 Oct;31:119-123. doi: 10.1016/j.parkreldis.2016.07.013. Epub 2016 Jul 25. Parkinsonism Relat Disord. 2016. PMID: 27477622

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