Klein C - Search Results

1

Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation.

Doss S, Lohmann K, Seibler P, Arns B, Klopstock T, Zühlke C, Freimann K, Winkler S, Lohnau T, Drungowski M, Nürnberg P, Wiegers K, Lohmann E, Naz S, Kasten M, Bohner G, Ramirez A, Endres M, Klein C. Doss S, et al. Among authors: klein c. J Neurol. 2014 Jan;261(1):207-12. doi: 10.1007/s00415-013-7177-7. Epub 2013 Nov 8. J Neurol. 2014. PMID: 24202787

2

Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.

Klein C, Pramstaller PP, Castellan CC, Breakefield XO, Kramer PL, Ozelius LJ. Klein C, et al. Ann Neurol. 1998 Sep;44(3):394-8. doi: 10.1002/ana.410440318. Ann Neurol. 1998. PMID: 9749609

3

Genetic analysis of three patients with an 18p- syndrome and dystonia.

Klein C, Page CE, LeWitt P, Gordon MF, de Leon D, Awaad Y, Breakefield XO, Brin MF, Ozelius LJ. Klein C, et al. Neurology. 1999 Feb;52(3):649-51. doi: 10.1212/wnl.52.3.649. Neurology. 1999. PMID: 10025808

4

Parkinson's disease in twins: a follow-up study.

Vieregge P, Hagenah J, Heberlein I, Klein C, Ludin HP. Vieregge P, et al. Among authors: klein c. Neurology. 1999 Aug 11;53(3):566-72. doi: 10.1212/wnl.53.3.566. Neurology. 1999. PMID: 10449122

5

The GAG deletion of the DYT1 gene is infrequent in musicians with focal dystonia.

Friedman JR, Klein C, Leung J, Woodward H, Ozelius LJ, Breakefield XO, Charness ME. Friedman JR, et al. Among authors: klein c. Neurology. 2000 Nov 14;55(9):1417-8. doi: 10.1212/wnl.55.9.1417. Neurology. 2000. PMID: 11087801 No abstract available.

6

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene.

Hilker R, Klein C, Ghaemi M, Kis B, Strotmann T, Ozelius LJ, Lenz O, Vieregge P, Herholz K, Heiss WD, Pramstaller PP. Hilker R, et al. Among authors: klein c. Ann Neurol. 2001 Mar;49(3):367-76. Ann Neurol. 2001. PMID: 11261512

7

Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence.

Saunders-Pullman R, Shriberg J, Heiman G, Raymond D, Wendt K, Kramer P, Schilling K, Kurlan R, Klein C, Ozelius LJ, Risch NJ, Bressman SB. Saunders-Pullman R, et al. Among authors: klein c. Neurology. 2002 Jan 22;58(2):242-5. doi: 10.1212/wnl.58.2.242. Neurology. 2002. PMID: 11805251

8

Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations.

Hedrich K, Marder K, Harris J, Kann M, Lynch T, Meija-Santana H, Pramstaller PP, Schwinger E, Bressman SB, Fahn S, Klein C. Hedrich K, et al. Among authors: klein c. Neurology. 2002 Apr 23;58(8):1239-46. doi: 10.1212/wnl.58.8.1239. Neurology. 2002. PMID: 11971093

9

Genetics of primary dystonia.

Klein C, Breakefield XO, Ozelius LJ. Klein C, et al. Semin Neurol. 1999;19(3):271-80. doi: 10.1055/s-2008-1040843. Semin Neurol. 1999. PMID: 12194383 Review.

10

Phenotypic features of myoclonus-dystonia in three kindreds.

Doheny DO, Brin MF, Morrison CE, Smith CJ, Walker RH, Abbasi S, Müller B, Garrels J, Liu L, De Carvalho Aguiar P, Schilling K, Kramer P, De Leon D, Raymond D, Saunders-Pullman R, Klein C, Bressman SB, Schmand B, Tijssen MA, Ozelius LJ, Silverman JM. Doheny DO, et al. Among authors: klein c. Neurology. 2002 Oct 22;59(8):1187-96. doi: 10.1212/wnl.59.8.1187. Neurology. 2002. PMID: 12391346

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