Klein C - Search Results

1

Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotype.

van Nuenen BF, Weiss MM, Bloem BR, Reetz K, van Eimeren T, Lohmann K, Hagenah J, Pramstaller PP, Binkofski F, Klein C, Siebner HR. van Nuenen BF, et al. Among authors: klein c. Neurology. 2009 Mar 24;72(12):1041-7. doi: 10.1212/01.wnl.0000338699.56379.11. Epub 2008 Nov 26. Neurology. 2009. PMID: 19038850 Free PMC article.

2

The diagnosis of 'essential palatal tremor'.

Vieregge P, Klein C, Gehrking E, Körtke D, Kömpf D. Vieregge P, et al. Among authors: klein c. Neurology. 1997 Jul;49(1):248-9. doi: 10.1212/wnl.49.1.248. Neurology. 1997. PMID: 9222198

3

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

4

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.

5

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

6

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

7

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

8

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

9

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.

10

[Genetics of dystonia].

Klein C, Kann M, Kis B, Pramstaller PP, Breakefield XO, Ozelius LJ, Vieregge P. Klein C, et al. Nervenarzt. 2000 Jun;71(6):431-41. doi: 10.1007/s001150050604. Nervenarzt. 2000. PMID: 10919137 Review. German.

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