Klein C - Search Results

1

Rapid-onset dystonia-parkinsonism: linkage to chromosome 19q13.

Kramer PL, Mineta M, Klein C, Schilling K, de Leon D, Farlow MR, Breakefield XO, Bressman SB, Dobyns WB, Ozelius LJ, Brashear A. Kramer PL, et al. Among authors: klein c. Ann Neurol. 1999 Aug;46(2):176-82. doi: 10.1002/1531-8249(199908)46:2<176::aid-ana6>3.0.co;2-2. Ann Neurol. 1999. PMID: 10443882

2

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.

Klein C, Brin MF, de Leon D, Limborska SA, Ivanova-Smolenskaya IA, Bressman SB, Friedman A, Markova ED, Risch NJ, Breakefield XO, Ozelius LJ. Klein C, et al. Hum Mol Genet. 1998 Jul;7(7):1133-6. doi: 10.1093/hmg/7.7.1133. Hum Mol Genet. 1998. PMID: 9618171

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

Search for a founder mutation in idiopathic focal dystonia from Northern Germany.

Klein C, Ozelius LJ, Hagenah J, Breakefield XO, Risch NJ, Vieregge P. Klein C, et al. Am J Hum Genet. 1998 Dec;63(6):1777-82. doi: 10.1086/302143. Am J Hum Genet. 1998. PMID: 9837831 Free PMC article.

6

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

7

Association of a missense change in the D2 dopamine receptor with myoclonus dystonia.

Klein C, Brin MF, Kramer P, Sena-Esteves M, de Leon D, Doheny D, Bressman S, Fahn S, Breakefield XO, Ozelius LJ. Klein C, et al. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5173-6. doi: 10.1073/pnas.96.9.5173. Proc Natl Acad Sci U S A. 1999. PMID: 10220438 Free PMC article.

8

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

9

Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.

Nygaard TG, Raymond D, Chen C, Nishino I, Greene PE, Jennings D, Heiman GA, Klein C, Saunders-Pullman RJ, Kramer P, Ozelius LJ, Bressman SB. Nygaard TG, et al. Among authors: klein c. Ann Neurol. 1999 Nov;46(5):794-8. doi: 10.1002/1531-8249(199911)46:5<794::aid-ana19>3.0.co;2-2. Ann Neurol. 1999. PMID: 10554001

10

Concordant late onset of craniocervical dystonia in a pair of monozygotic twins.

Sieberer MG, Vieregge P, Klein C, Ozelius LJ, Wandinger KP. Sieberer MG, et al. Among authors: klein c. Mov Disord. 1999 Nov;14(6):1040-3. doi: 10.1002/1531-8257(199911)14:6<1040::aid-mds1025>3.0.co;2-9. Mov Disord. 1999. PMID: 10584687 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

4,010 results

Search Page

Filters