Klein C - Search Results

1

Structural imaging in the presymptomatic stage of genetically determined parkinsonism.

Reetz K, Tadic V, Kasten M, Brüggemann N, Schmidt A, Hagenah J, Pramstaller PP, Ramirez A, Behrens MI, Siebner HR, Klein C, Binkofski F. Reetz K, et al. Among authors: klein c. Neurobiol Dis. 2010 Sep;39(3):402-8. doi: 10.1016/j.nbd.2010.05.006. Epub 2010 May 17. Neurobiol Dis. 2010. PMID: 20483373

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

Exclusion of chromosome regions 6p12 and 15q11, but not chromosome region 7p11, in a German family with autosomal dominant congenital nystagmus.

Klein C, Vieregge P, Heide W, Kemper B, Hagedorn-Greiwe M, Hagenah J, Vollmer C, Breakefield XO, Kömpf D, Ozelius L. Klein C, et al. Genomics. 1998 Nov 15;54(1):176-7. doi: 10.1006/geno.1998.5535. Genomics. 1998. PMID: 9806847 No abstract available.

4

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

5

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

6

Genetic testing for early-onset torsion dystonia (DYT1): introduction of a simple screening method, experiences from testing of a large patient cohort, and ethical aspects.

Klein C, Friedman J, Bressman S, Vieregge P, Brin MF, Pramstaller PP, De Leon D, Hagenah J, Sieberer M, Fleet C, Kiely R, Xin W, Breakefield XO, Ozelius LJ, Sims KB. Klein C, et al. Genet Test. 1999;3(4):323-8. doi: 10.1089/gte.1999.3.323. Genet Test. 1999. PMID: 10627938

7

Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype.

Klein C, Pramstaller PP, Kis B, Page CC, Kann M, Leung J, Woodward H, Castellan CC, Scherer M, Vieregge P, Breakefield XO, Kramer PL, Ozelius LJ. Klein C, et al. Ann Neurol. 2000 Jul;48(1):65-71. Ann Neurol. 2000. PMID: 10894217

8

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.

9

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

10

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism.

Hedrich K, Kann M, Lanthaler AJ, Dalski A, Eskelson C, Landt O, Schwinger E, Vieregge P, Lang AE, Breakefield XO, Ozelius LJ, Pramstaller PP, Klein C. Hedrich K, et al. Among authors: klein c. Hum Mol Genet. 2001 Aug 1;10(16):1649-56. doi: 10.1093/hmg/10.16.1649. Hum Mol Genet. 2001. PMID: 11487568

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