Klein C - Search Results

1

Primary familial brain calcification with known gene mutations: a systematic review and challenges of phenotypic characterization.

Tadic V, Westenberger A, Domingo A, Alvarez-Fischer D, Klein C, Kasten M. Tadic V, et al. Among authors: klein c. JAMA Neurol. 2015 Apr;72(4):460-7. doi: 10.1001/jamaneurol.2014.3889. JAMA Neurol. 2015. PMID: 25686319 Review.

2

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

3

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

4

Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations.

Hedrich K, Marder K, Harris J, Kann M, Lynch T, Meija-Santana H, Pramstaller PP, Schwinger E, Bressman SB, Fahn S, Klein C. Hedrich K, et al. Among authors: klein c. Neurology. 2002 Apr 23;58(8):1239-46. doi: 10.1212/wnl.58.8.1239. Neurology. 2002. PMID: 11971093

5

Mutations in DYT1: extension of the phenotypic and mutational spectrum.

Kabakci K, Hedrich K, Leung JC, Mitterer M, Vieregge P, Lencer R, Hagenah J, Garrels J, Witt K, Klostermann F, Svetel M, Friedman J, Kostic V, Bressman SB, Breakefield XO, Ozelius LJ, Pramstaller PP, Klein C. Kabakci K, et al. Among authors: klein c. Neurology. 2004 Feb 10;62(3):395-400. doi: 10.1212/01.wnl.0000113024.84178.f7. Neurology. 2004. PMID: 14872019

6

Myoclonus-dystonia: detection of novel, recurrent, and de novo SGCE mutations.

Hedrich K, Meyer EM, Schüle B, Kock N, de Carvalho Aguiar P, Wiegers K, Koelman JH, Garrels J, Dürr R, Liu L, Schwinger E, Ozelius LJ, Landwehrmeyer B, Stoessl AJ, Tijssen MA, Klein C. Hedrich K, et al. Among authors: klein c. Neurology. 2004 Apr 13;62(7):1229-31. doi: 10.1212/01.wnl.0000118286.75059.35. Neurology. 2004. PMID: 15079037 No abstract available.

7

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

8

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

9

Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease.

Hedrich K, Winkler S, Hagenah J, Kabakci K, Kasten M, Schwinger E, Volkmann J, Pramstaller PP, Kostic V, Vieregge P, Klein C. Hedrich K, et al. Among authors: klein c. Mov Disord. 2006 Sep;21(9):1506-10. doi: 10.1002/mds.20990. Mov Disord. 2006. PMID: 16758483

10

Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?

Hedrich K, Hagenah J, Djarmati A, Hiller A, Lohnau T, Lasek K, Grünewald A, Hilker R, Steinlechner S, Boston H, Kock N, Schneider-Gold C, Kress W, Siebner H, Binkofski F, Lencer R, Münchau A, Klein C. Hedrich K, et al. Among authors: klein c. Arch Neurol. 2006 Jun;63(6):833-8. doi: 10.1001/archneur.63.6.833. Arch Neurol. 2006. PMID: 16769864

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