Tunc S - Search Results

1

Quantitative susceptibility mapping reveals alterations of dentate nuclei in common types of degenerative cerebellar ataxias.

Deistung A, Jäschke D, Draganova R, Pfaffenrot V, Hulst T, Steiner KM, Thieme A, Giordano IA, Klockgether T, Tunc S, Münchau A, Minnerop M, Göricke SL, Reichenbach JR, Timmann D. Deistung A, et al. Among authors: tunc s. Brain Commun. 2022 Jan 13;4(1):fcab306. doi: 10.1093/braincomms/fcab306. eCollection 2022. Brain Commun. 2022. PMID: 35291442 Free PMC article.

2

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.

3

[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.

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

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

8

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.

9

"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.

10

Reply to: Double Trouble from POLG1 and CLCN1 Variants with Intrafamilial Phenotypic Heterogeneity.

Pauly MG, Tunc S, Bäumer T, Gillessen-Kaesbach G, Münchau A. Pauly MG, et al. Among authors: tunc s. Mov Disord Clin Pract. 2020 May 8;7(5):577-578. doi: 10.1002/mdc3.12961. eCollection 2020 Jul. Mov Disord Clin Pract. 2020. PMID: 32626811 Free PMC article. No abstract available.

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