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Items: 1 to 20 of 28

1.

'Atypical' Parkinson's disease - genetic.

Weissbach A, Wittke C, Kasten M, Klein C.

Int Rev Neurobiol. 2019;149:207-235. doi: 10.1016/bs.irn.2019.10.011. Epub 2019 Nov 25.

PMID:
31779813
2.

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.

Neuroimage Clin. 2019;24:102043. doi: 10.1016/j.nicl.2019.102043. Epub 2019 Oct 18.

3.

Temporal discrimination threshold and blink reflex recovery cycle in cervical dystonia - two sides of the same coin?

Junker J, Paulus T, Brandt V, Weissbach A, Tunc S, Loens S, Reilly RB, Hutchinson M, Baumer T.

Parkinsonism Relat Disord. 2019 Nov;68:4-7. doi: 10.1016/j.parkreldis.2019.09.028. Epub 2019 Sep 28.

PMID:
31621616
4.

Single-pulse subthalamic deep brain stimulation reduces premotor-motor facilitation in Parkinson's disease.

Weissbach A, Udupa K, Ni Z, Gunraj C, Rinchon C, Baarbe J, Fasano A, Munhoz RP, Lang A, Tadic V, Brüggemann N, Münchau A, Bäumer T, Chen R.

Parkinsonism Relat Disord. 2019 Sep;66:224-227. doi: 10.1016/j.parkreldis.2019.08.003. Epub 2019 Aug 7.

PMID:
31427071
5.

Somatosensory-motor cortex interactions measured using dual-site transcranial magnetic stimulation.

Brown MJN, Weissbach A, Pauly MG, Vesia M, Gunraj C, Baarbé J, Münchau A, Bäumer T, Chen R.

Brain Stimul. 2019 Sep - Oct;12(5):1229-1243. doi: 10.1016/j.brs.2019.04.009. Epub 2019 Apr 23.

PMID:
31043330
6.

Association of Pallidal Neurostimulation and Outcome Predictors With X-linked Dystonia Parkinsonism.

Brüggemann N, Domingo A, Rasche D, Moll CKE, Rosales RL, Jamora RDG, Hanssen H, Münchau A, Graf J, Weissbach A, Tadic V, Diesta CC, Volkmann J, Kühn A, Münte TF, Tronnier V, Klein C.

JAMA Neurol. 2019 Feb 1;76(2):211-216. doi: 10.1001/jamaneurol.2018.3777.

7.

Predictors of alcohol responsiveness in dystonia.

Junker J, Brandt V, Berman BD, Vidailhet M, Roze E, Weissbach A, Comella C, Malaty IA, Jankovic J, LeDoux MS, Berardelli A, Barbano R, Reich SG, Perlmutter JS, Jinnah HA, Brüggemann N.

Neurology. 2018 Nov 20;91(21):e2020-e2026. doi: 10.1212/WNL.0000000000006551. Epub 2018 Oct 19.

8.

Associative plasticity in supplementary motor area - motor cortex pathways in Tourette syndrome.

Tübing J, Gigla B, Brandt VC, Verrel J, Weissbach A, Beste C, Münchau A, Bäumer T.

Sci Rep. 2018 Aug 10;8(1):11984. doi: 10.1038/s41598-018-30504-8.

9.

Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.

Hebert E, Borngräber F, Schmidt A, Rakovic A, Brænne I, Weissbach A, Hampf J, Vollstedt EJ, Größer L, Schaake S, Müller M, Manzoor H, Jabusch HC, Alvarez-Fischer D, Kasten M, Kostic VS, Gasser T, Zeuner KE, Kim HJ, Jeon B, Bauer P, Altenmüller E, Klein C, Lohmann K.

Genes (Basel). 2017 Oct 18;8(10). pii: E276. doi: 10.3390/genes8100276. Review.

10.

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.

Ann Neurol. 2017 Oct;82(4):543-553. doi: 10.1002/ana.25035. Epub 2017 Sep 25.

PMID:
28869676
11.

Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers.

Weissbach A, König IR, Hückelheim K, Pramstaller PP, Werner E, Brüggemann N, Tadic V, Lohmann K, Bäumer T, Münchau A, Kasten M, Klein C.

Parkinsonism Relat Disord. 2017 Sep;42:95-99. doi: 10.1016/j.parkreldis.2017.07.003. Epub 2017 Jul 8.

PMID:
28716427
12.

Faithful SGCE imprinting in iPSC-derived cortical neurons: an endogenous cellular model of myoclonus-dystonia.

Grütz K, Seibler P, Weissbach A, Lohmann K, Carlisle FA, Blake DJ, Westenberger A, Klein C, Grünewald A.

Sci Rep. 2017 Feb 3;7:41156. doi: 10.1038/srep41156.

13.

Alternating Hemiplegia of Childhood as a New Presentation of Adenylate Cyclase 5-Mutation-Associated Disease: A Report of Two Cases.

Westenberger A, Max C, Brüggemann N, Domingo A, Grütz K, Pawlack H, Weissbach A, Kühn AA, Spiegler J, Lang AE, Sperner J, Fung VSC, Schallner J, Gillessen-Kaesbach G, Münchau A, Klein C.

J Pediatr. 2017 Feb;181:306-308.e1. doi: 10.1016/j.jpeds.2016.10.079. Epub 2016 Dec 6.

PMID:
27931826
14.

Abnormal premotor-motor interaction in heterozygous Parkin- and Pink1 mutation carriers.

Weissbach A, Bäumer T, Pramstaller PP, Brüggemann N, Tadic V, Chen R, Klein C, Münchau A.

Clin Neurophysiol. 2017 Jan;128(1):275-280. doi: 10.1016/j.clinph.2016.10.007. Epub 2016 Oct 26.

PMID:
27843055
15.

Clinical and genetic features of cervical dystonia in a large multicenter cohort.

LeDoux MS, Vemula SR, Xiao J, Thompson MM, Perlmutter JS, Wright LJ, Jinnah HA, Rosen AR, Hedera P, Comella CL, Weissbach A, Junker J, Jankovic J, Barbano RL, Reich SG, Rodriguez RL, Berman BD, Chouinard S, Severt L, Agarwal P, Stover NP.

Neurol Genet. 2016 Apr 11;2(3):e69. doi: 10.1212/NXG.0000000000000069. eCollection 2016 Jun.

16.

A nonsense mutation in CHCHD2 in a patient with Parkinson disease.

Koschmidder E, Weissbach A, Brüggemann N, Kasten M, Klein C, Lohmann K.

Neurology. 2016 Feb 9;86(6):577-9. doi: 10.1212/WNL.0000000000002361. Epub 2016 Jan 13. No abstract available.

PMID:
26764027
17.

Premotor-motor excitability is altered in dopa-responsive dystonia.

Weissbach A, Bäumer T, Brüggemann N, Tadic V, Zittel S, Cheng B, Thomalla G, Klein C, Münchau A.

Mov Disord. 2015 Oct;30(12):1705-9. doi: 10.1002/mds.26365. Epub 2015 Jul 31.

PMID:
26230973
18.

The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort.

Mencacci NE, R'bibo L, Bandres-Ciga S, Carecchio M, Zorzi G, Nardocci N, Garavaglia B, Batla A, Bhatia KP, Pittman AM, Hardy J, Weissbach A, Klein C, Gasser T, Lohmann E, Wood NW.

Hum Mol Genet. 2015 Sep 15;24(18):5326-9. doi: 10.1093/hmg/ddv255. Epub 2015 Jul 8.

19.

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.

Mencacci NE, Rubio-Agusti I, Zdebik A, Asmus F, Ludtmann MH, Ryten M, Plagnol V, Hauser AK, Bandres-Ciga S, Bettencourt C, Forabosco P, Hughes D, Soutar MM, Peall K, Morris HR, Trabzuni D, Tekman M, Stanescu HC, Kleta R, Carecchio M, Zorzi G, Nardocci N, Garavaglia B, Lohmann E, Weissbach A, Klein C, Hardy J, Pittman AM, Foltynie T, Abramov AY, Gasser T, Bhatia KP, Wood NW.

Am J Hum Genet. 2015 Jun 4;96(6):938-47. doi: 10.1016/j.ajhg.2015.04.008. Epub 2015 May 14.

20.

Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease.

Weissbach A, Bäumer T, Rosales R, Lee LV, Brüggemann N, Domingo A, Westenberger A, Jamora RD, Diesta CC, Brandt V, Tadic V, Zittel S, Klein C, Münchau A.

Mov Disord. 2015 May;30(6):873-5. doi: 10.1002/mds.26224. Epub 2015 Apr 25. No abstract available.

PMID:
25914216

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