Klein C - Search Results

1

Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.

Clark LN, Haamer E, Mejia-Santana H, Harris J, Lesage S, Durr A, Bs SJ, Hedrich K, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Scott W, Klein C, Brice A, Roomere H, Ottman R, Marder K. Clark LN, et al. Among authors: klein c. Mov Disord. 2007 May 15;22(7):932-7. doi: 10.1002/mds.21419. Mov Disord. 2007. PMID: 17415800

2

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

3

Parkin mutations in a patient with hemiparkinsonism-hemiatrophy: a clinical-genetic and PET study.

Pramstaller PP, Künig G, Leenders K, Kann M, Hedrich K, Vieregge P, Goetz CG, Klein C. Pramstaller PP, et al. Among authors: klein c. Neurology. 2002 Mar 12;58(5):808-10. doi: 10.1212/wnl.58.5.808. Neurology. 2002. PMID: 11889248

4

The parkin gene is not involved in late-onset Parkinson's disease.

Kann M, Hedrich K, Vieregge P, Jacobs H, Müller B, Kock N, Schwinger E, Klein C, Marder K, Harris J, Meija-Santana H, Bressman S, Ozelius LJ, Lang AE, Pramstaller PP. Kann M, et al. Among authors: klein c. Neurology. 2002 Mar 12;58(5):835; author reply 835. doi: 10.1212/wnl.58.5.835. Neurology. 2002. PMID: 11889262 No abstract available.

5

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

6

Parkin-proven disease: common founders but divergent phenotypes.

Lincoln S, Wiley J, Lynch T, Langston JW, Chen R, Lang A, Rogaeva E, Sa DS, Munhoz RP, Harris J, Marder K, Klein C, Bisceglio G, Hussey J, West A, Hulihan M, Hardy J, Farrer M. Lincoln S, et al. Among authors: klein c. Neurology. 2003 May 27;60(10):1605-10. doi: 10.1212/01.wnl.0000064289.49410.a9. Neurology. 2003. PMID: 12771249

7

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

Hedrich K, Djarmati A, Schäfer N, Hering R, Wellenbrock C, Weiss PH, Hilker R, Vieregge P, Ozelius LJ, Heutink P, Bonifati V, Schwinger E, Lang AE, Noth J, Bressman SB, Pramstaller PP, Riess O, Klein C. Hedrich K, et al. Among authors: klein c. Neurology. 2004 Feb 10;62(3):389-94. doi: 10.1212/01.wnl.0000113022.51739.88. Neurology. 2004. PMID: 14872018

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

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study.

Karamohamed S, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Liu J, Shoemaker CM, Wilk JB, DeStefano AL, Latourelle JC, Xu G, Watts R, Growdon J, Lew M, Waters C, Vieregge P, Pramstaller PP, Klein C, Racette BA, Perlmutter JS, Parsian A, Singer C, Montgomery E, Baker K, Gusella JF, Herbert A, Myers RH. Karamohamed S, et al. Among authors: klein c. Mov Disord. 2005 Sep;20(9):1188-91. doi: 10.1002/mds.20515. Mov Disord. 2005. PMID: 15966003

10

Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers.

Pramstaller PP, Schlossmacher MG, Jacques TS, Scaravilli F, Eskelson C, Pepivani I, Hedrich K, Adel S, Gonzales-McNeal M, Hilker R, Kramer PL, Klein C. Pramstaller PP, et al. Among authors: klein c. Ann Neurol. 2005 Sep;58(3):411-22. doi: 10.1002/ana.20587. Ann Neurol. 2005. PMID: 16130111

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