Bürk K - Search Results

1

The comorbidity and co-medication profile of patients with progressive supranuclear palsy.

Greten S, Wegner F, Jensen I, Krey L, Rogozinski S, Fehring M, Heine J, Doll-Lee J, Pötter-Nerger M, Zeitzschel M, Hagena K, Pedrosa DJ, Eggers C, Bürk K, Trenkwalder C, Claus I, Warnecke T, Süß P, Winkler J, Gruber D, Gandor F, Berg D, Paschen S, Classen J, Pinkhardt EH, Kassubek J, Jost WH, Tönges L, Kühn AA, Schwarz J, Peters O, Dashti E, Priller J, Spruth EJ, Krause P, Spottke A, Schneider A, Beyle A, Kimmich O, Donix M, Haussmann R, Brandt M, Dinter E, Wiltfang J, Schott BH, Zerr I, Bähr M, Buerger K, Janowitz D, Perneczky R, Rauchmann BS, Weidinger E, Levin J, Katzdobler S, Düzel E, Glanz W, Teipel S, Kilimann I, Prudlo J, Gasser T, Brockmann K, Hoffmann DC, Klockgether T, Krause O, Heck J, Höglinger GU, Klietz M. Greten S, et al. Among authors: burk k. J Neurol. 2024 Feb;271(2):782-793. doi: 10.1007/s00415-023-12006-4. Epub 2023 Oct 6. J Neurol. 2024. PMID: 37803149 Free PMC article.

2

The Progressive Supranuclear Palsy Clinical Deficits Scale.

Piot I, Schweyer K, Respondek G, Stamelou M; DescribePSP study group; ProPSP study group; MDS-endorsed PSP study group; Sckopke P, Schenk T, Goetz CG, Stebbins GT, Höglinger GU. Piot I, et al. Mov Disord. 2020 Apr;35(4):650-661. doi: 10.1002/mds.27964. Epub 2020 Jan 17. Mov Disord. 2020. PMID: 31951049

3

Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3.

Abele M, Bürk K, Laccone F, Dichgans J, Klockgether T. Abele M, et al. Among authors: burk k. J Neurol. 2001 Apr;248(4):311-4. doi: 10.1007/s004150170206. J Neurol. 2001. PMID: 11374096

4

Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families.

Dichgans M, Schöls L, Herzog J, Stevanin G, Weirich-Schwaiger H, Rouleau G, Bürk K, Klockgether T, Zühlke C, Laccone F, Riess O, Gasser T. Dichgans M, et al. Among authors: burk k. Neurology. 1999 Mar 10;52(4):849-51. doi: 10.1212/wnl.52.4.849. Neurology. 1999. PMID: 10078738

5

Cerebellar ataxia with glutamic acid decarboxylase autoantibodies.

Abele M, Weller M, Mescheriakov S, Bürk K, Dichgans J, Klockgether T. Abele M, et al. Among authors: burk k. Neurology. 1999 Mar 10;52(4):857-9. doi: 10.1212/wnl.52.4.857. Neurology. 1999. PMID: 10078741

6

Nerve conduction studies in multiple system atrophy.

Abele M, Schulz JB, Bürk K, Topka H, Dichgans J, Klockgether T. Abele M, et al. Among authors: burk k. Eur Neurol. 2000;43(4):221-3. doi: 10.1159/000008179. Eur Neurol. 2000. PMID: 10828652

7

Clinical and genetic analysis of three German kindreds with autosomal dominant cerebellar ataxia type I linked to the SCA2 locus.

Bürk K, Stevanin G, Didierjean O, Cancel G, Trottier Y, Skalej M, Abele M, Brice A, Dichgans J, Klockgether T. Bürk K, et al. J Neurol. 1997 Apr;244(4):256-61. doi: 10.1007/s004150050081. J Neurol. 1997. PMID: 9112595

8

Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.

Bürk K, Fetter M, Abele M, Laccone F, Brice A, Dichgans J, Klockgether T. Bürk K, et al. J Neurol. 1999 Sep;246(9):789-97. doi: 10.1007/s004150050456. J Neurol. 1999. PMID: 10525976 Clinical Trial.

9

Cognitive deficits in spinocerebellar ataxia type 1, 2, and 3.

Bürk K, Globas C, Bösch S, Klockgether T, Zühlke C, Daum I, Dichgans J. Bürk K, et al. J Neurol. 2003 Feb;250(2):207-11. doi: 10.1007/s00415-003-0976-5. J Neurol. 2003. PMID: 12574952 Clinical Trial.

10

Friedreich's ataxia with retained tendon reflexes: molecular genetics, clinical neurophysiology, and magnetic resonance imaging.

Klockgether T, Zühlke C, Schulz JB, Bürk K, Fetter M, Dittmann H, Skalej M, Dichgans J. Klockgether T, et al. Among authors: burk k. Neurology. 1996 Jan;46(1):118-21. doi: 10.1212/wnl.46.1.118. Neurology. 1996. PMID: 8559357

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