Klein C - Search Results

1

Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.

Lange LM, Junker J, Loens S, Baumann H, Olschewski L, Schaake S, Madoev H, Petkovic S, Kuhnke N, Kasten M, Westenberger A, Domingo A, Marras C, König IR, Camargos S, Ozelius LJ, Klein C, Lohmann K. Lange LM, et al. Among authors: klein c. Mov Disord. 2021 May;36(5):1086-1103. doi: 10.1002/mds.28485. Epub 2021 Jan 27. Mov Disord. 2021. PMID: 33502045 Review.

2

Paroxysmal choreoathetosis in a patient with idiopathic basal ganglia calcification, chorea, and dystonia.

Klein C, Vieregge P, Kömpf D. Klein C, et al. Mov Disord. 1997 Mar;12(2):254-5. doi: 10.1002/mds.870120223. Mov Disord. 1997. PMID: 9087991 No abstract available.

3

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

4

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

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

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

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.

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