Zühlke C - Search Results

1

Psychosis Complicating Friedreich Ataxia.

Ganos C, Schöttle D, Zühlke C, Münchau A. Ganos C, et al. Among authors: zuhlke c. Mov Disord Clin Pract. 2014 Nov 28;2(1):84-85. doi: 10.1002/mdc3.12115. eCollection 2015 Mar. Mov Disord Clin Pract. 2014. PMID: 30363893 Free PMC article. No abstract available.

2

Clinical and neurophysiological profile of four German families with spinocerebellar ataxia type 14.

Ganos C, Zittel S, Minnerop M, Schunke O, Heinbokel C, Gerloff C, Zühlke C, Bauer P, Klockgether T, Münchau A, Bäumer T. Ganos C, et al. Among authors: zuhlke c. Cerebellum. 2014 Feb;13(1):89-96. doi: 10.1007/s12311-013-0522-7. Cerebellum. 2014. PMID: 24030789

3

Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromes.

Gisatulin M, Dobricic V, Zühlke C, Hellenbroich Y, Tadic V, Münchau A, Isenhardt K, Bürk K, Bahlo M, Lockhart PJ, Lohmann K, Helmchen C, Brüggemann N. Gisatulin M, et al. Among authors: zuhlke c. Neurology. 2020 Nov 24;95(21):e2912-e2923. doi: 10.1212/WNL.0000000000010744. Epub 2020 Sep 1. Neurology. 2020. PMID: 32873692

4

Possible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.

Weissbach A, Djarmati A, Klein C, Dragasević N, Zühlke C, Raković A, Guzvić M, Butz E, Tönnies H, Siebert R, Petrović I, Svetel M, Kostić VS, Lohmann K. Weissbach A, et al. Among authors: zuhlke c. Mov Disord. 2010 Aug 15;25(11):1577-82. doi: 10.1002/mds.22857. Mov Disord. 2010. PMID: 20589871

5

Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18-Year Study.

Rosenbohm A, Pott H, Thomsen M, Rafehi H, Kaya S, Szymczak S, Volk AE, Mueller K, Silveira I, Weishaupt JH, Tönnies H, Seibler P, Zschiedrich K, Schaake S, Westenberger A, Zühlke C, Depienne C, Trinh J, Ludolph AC, Klein C, Bahlo M, Lohmann K. Rosenbohm A, et al. Among authors: zuhlke c. Mov Disord. 2022 Dec;37(12):2427-2439. doi: 10.1002/mds.29221. Epub 2022 Sep 23. Mov Disord. 2022. PMID: 36148898 Free PMC article.

6

Focal dystonia as a presenting sign of spinocerebellar ataxia 17.

Hagenah JM, Zühlke C, Hellenbroich Y, Heide W, Klein C. Hagenah JM, et al. Among authors: zuhlke c. Mov Disord. 2004 Feb;19(2):217-20. doi: 10.1002/mds.10600. Mov Disord. 2004. PMID: 14978680

7

Premutations in the FMR1 gene as a modifying factor in Parkin-associated Parkinson's disease?

Hedrich K, Pramstaller PP, Stübke K, Hiller A, Kabakci K, Purmann S, Kasten M, Scaglione C, Schwinger E, Volkmann J, Kostic V, Vieregge P, Martinelli P, Abbruzzese G, Klein C, Zühlke C. Hedrich K, et al. Among authors: zuhlke c. Mov Disord. 2005 Aug;20(8):1060-2. doi: 10.1002/mds.20512. Mov Disord. 2005. PMID: 15929093

8

No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3.

Hellenbroich Y, Kaulich M, Opitz S, Schwinger E, Zühlke C. Hellenbroich Y, et al. Among authors: zuhlke c. Psychiatr Genet. 2004 Jun;14(2):61-3. doi: 10.1097/01.ypg.0000128763.69225.77. Psychiatr Genet. 2004. PMID: 15167689

9

Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein.

Zühlke C, Bürk K. Zühlke C, et al. Cerebellum. 2007;6(4):300-7. doi: 10.1080/14734220601136177. Epub 2007 Jan 19. Cerebellum. 2007. PMID: 17853080 Review.

10

Do CTG expansions at the SCA8 locus cause ataxia?

Schöls L, Bauer I, Zühlke C, Schulte T, Kölmel C, Bürk K, Topka H, Bauer P, Przuntek H, Riess O. Schöls L, et al. Among authors: zuhlke c. Ann Neurol. 2003 Jul;54(1):110-5. doi: 10.1002/ana.10608. Ann Neurol. 2003. PMID: 12838526

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