Tunc S - Search Results

1

Hope for Huntington's disease? A novel approach for disease modification.

Tunc S, Capetian P, Münchau A. Tunc S, et al. Mov Disord. 2014 Aug;29(9):1117. doi: 10.1002/mds.25935. Epub 2014 Jun 7. Mov Disord. 2014. PMID: 24909788 No abstract available.

2

[On the fast track to diagnosis : Recommendations for patients without a diagnosis].

Stieber C, Mücke M, Windheuser IC, Grigull L, Klawonn F, Tunc S, Münchau A, Klockgether T. Stieber C, et al. Among authors: tunc s. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2017 May;60(5):517-522. doi: 10.1007/s00103-017-2535-8. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2017. PMID: 28289775 German.

3

Facial twitches in ADCY5-associated disease - Myokymia or myoclonus? An electromyography study.

Tunc S, Brüggemann N, Baaske MK, Hartmann C, Grütz K, Westenberger A, Klein C, Münchau A, Bäumer T. Tunc S, et al. Parkinsonism Relat Disord. 2017 Jul;40:73-75. doi: 10.1016/j.parkreldis.2017.04.013. Epub 2017 Apr 20. Parkinsonism Relat Disord. 2017. PMID: 28442302

4

Alcohol improves cerebellar learning deficit in myoclonus-dystonia: A clinical and electrophysiological investigation.

Weissbach A, Werner E, Bally JF, Tunc S, Löns S, Timmann D, Zeuner KE, Tadic V, Brüggemann N, Lang A, Klein C, Münchau A, Bäumer T. Weissbach A, et al. Among authors: tunc s. Ann Neurol. 2017 Oct;82(4):543-553. doi: 10.1002/ana.25035. Epub 2017 Sep 25. Ann Neurol. 2017. PMID: 28869676

5

A novel, in-frame KMT2B deletion in a patient with apparently isolated, generalized dystonia.

Lange LM, Tunc S, Tennstedt S, Münchau A, Klein C, Assmann B, Lohmann K. Lange LM, et al. Among authors: tunc s. Mov Disord. 2017 Oct;32(10):1495-1497. doi: 10.1002/mds.27137. Epub 2017 Sep 18. Mov Disord. 2017. PMID: 28921672 No abstract available.

6

Boys in a famous choir: Singing and ticcing.

Tunc S, Münchau A. Tunc S, et al. Ann Neurol. 2017 Dec;82(6):1029-1031. doi: 10.1002/ana.25112. Ann Neurol. 2017. PMID: 29265544

7

A recurrent de-novo ANO3 mutation causes early-onset generalized dystonia.

Tunc S, Denecke J, Olschewski L, Bäumer T, Münchau A, Lessel D, Lohmann K. Tunc S, et al. J Neurol Sci. 2019 Jan 15;396:199-201. doi: 10.1016/j.jns.2018.11.024. Epub 2018 Nov 22. J Neurol Sci. 2019. PMID: 30502610 No abstract available.

8

Spinocerebellar Ataxia Type 28-Phenotypic and Molecular Characterization of a Family with Heterozygous and Compound-Heterozygous Mutations in AFG3L2.

Tunc S, Dulovic-Mahlow M, Baumann H, Baaske MK, Jahn M, Junker J, Münchau A, Brüggemann N, Lohmann K. Tunc S, et al. Cerebellum. 2019 Aug;18(4):817-822. doi: 10.1007/s12311-019-01036-2. Cerebellum. 2019. PMID: 31111429

9

Predictive coding and adaptive behavior in patients with genetically determined cerebellar ataxia--A neurophysiology study.

Tunc S, Baginski N, Lubs J, Bally JF, Weissbach A, Baaske MK, Tadic V, Brüggemann N, Bäumer T, Beste C, Münchau A. Tunc S, et al. Neuroimage Clin. 2019;24:102043. doi: 10.1016/j.nicl.2019.102043. Epub 2019 Oct 18. Neuroimage Clin. 2019. PMID: 31678909 Free PMC article.

10

"Twitching" and Stiffness in POLG1 Mutation Carriers: Red Flag or Red Herring?

Pauly MG, Tunc S, Bäumer T, Gillessen-Kaesbach G, Münchau A. Pauly MG, et al. Among authors: tunc s. Mov Disord Clin Pract. 2019 Nov 12;7(1):91-93. doi: 10.1002/mdc3.12860. eCollection 2020 Jan. Mov Disord Clin Pract. 2019. PMID: 31970219 Free PMC article. No abstract available.

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