Klein C - Search Results

1

No association between NOD2 variants and Parkinson's disease.

Appenzeller S, Thier S, Papengut F, Klein C, Hagenah J, Kasten M, Berg D, Srulijes K, Gasser T, Schreiber S, Deuschl G, Kuhlenbäumer G. Appenzeller S, et al. Among authors: klein c. Mov Disord. 2012 Aug;27(9):1191-2. doi: 10.1002/mds.25059. Epub 2012 Jul 13. Mov Disord. 2012. PMID: 22807259 No abstract available.

2

Exogenous levodopa is not toxic to elderly subjects with non-parkinsonian movement disorders: further clinical evidence.

Hagenah J, Klein C, Sieberer M, Vieregge P. Hagenah J, et al. Among authors: klein c. J Neural Transm (Vienna). 1999;106(3-4):301-7. doi: 10.1007/s007020050159. J Neural Transm (Vienna). 1999. PMID: 10392538

3

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

4

Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany.

Klein C, Vieregge P, Hagenah J, Sieberer M, Doyle E, Jacobs H, Gasser T, Breakefield XO, Risch NJ, Ozelius LJ. Klein C, et al. Ann Hum Genet. 1999 Jul;63(Pt 4):285-91. doi: 10.1046/j.1469-1809.1999.6340285.x. Ann Hum Genet. 1999. PMID: 10738540

5

Association studies of Parkinson's disease and parkin polymorphisms.

Klein C, Schumacher K, Jacobs H, Hagenah J, Kis B, Garrels J, Schwinger E, Ozelius L, Pramstaller P, Vieregge P, Kramer PL. Klein C, et al. Ann Neurol. 2000 Jul;48(1):126-7. Ann Neurol. 2000. PMID: 10894229 No abstract available.

6

Neuropsychological abnormalities in first degree relatives of patients with familial Parkinson's disease.

Kis B, Heberlein I, Hagenah J, Jacobs H, Klein C, Vieregge P. Kis B, et al. Among authors: klein c. J Neurol Neurosurg Psychiatry. 2000 Dec;69(6):838. doi: 10.1136/jnnp.69.6.838. J Neurol Neurosurg Psychiatry. 2000. PMID: 11185648 Free PMC article. No abstract available.

7

Focal and segmental primary dystonia in north-western Germany--a clinico-genetic study.

Maniak S, Sieberer M, Hagenah J, Klein C, Vieregge P. Maniak S, et al. Among authors: klein c. Acta Neurol Scand. 2003 Mar;107(3):228-32. doi: 10.1034/j.1600-0404.2003.01362.x. Acta Neurol Scand. 2003. PMID: 12614318

8

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: klein c. Mov Disord. 2004 Feb;19(2):217-20. doi: 10.1002/mds.10600. Mov Disord. 2004. PMID: 14978680

9

High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening.

Hagenah J, Saunders-Pullman R, Hedrich K, Kabakci K, Habermann K, Wiegers K, Mohrmann K, Lohnau T, Raymond D, Vieregge P, Nygaard T, Ozelius LJ, Bressman SB, Klein C. Hagenah J, et al. Among authors: klein c. Neurology. 2005 Mar 8;64(5):908-11. doi: 10.1212/01.WNL.0000152839.50258.A2. Neurology. 2005. PMID: 15753436

10

Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism.

Buhmann C, Binkofski F, Klein C, Büchel C, van Eimeren T, Erdmann C, Hedrich K, Kasten M, Hagenah J, Deuschl G, Pramstaller PP, Siebner HR. Buhmann C, et al. Among authors: klein c. Brain. 2005 Oct;128(Pt 10):2281-90. doi: 10.1093/brain/awh572. Epub 2005 Jun 9. Brain. 2005. PMID: 15947065

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