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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
Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.
Klein C, Gurvich N, Sena-Esteves M, Bressman S, Brin MF, Ebersole BJ, Fink S, Forsgren L, Friedman J, Grimes D, Holmgren G, Kyllerman M, Lang AE, de Leon D, Leung J, Prioleau C, Raymond D, Sanner G, Saunders-Pullman R, Vieregge P, Wahlström J, Breakefield XO, Kramer PL, Ozelius LJ, Sealfon SC. Klein C, et al. Ann Neurol. 2000 Mar;47(3):369-73. Ann Neurol. 2000. PMID: 10716258
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.
A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study.
Karamohamed S, DeStefano AL, Wilk JB, Shoemaker CM, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Sullivan KM, 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, Fink SJ, Myers RH, Herbert A; GenePD study. Karamohamed S, et al. Among authors: klein c. Neurology. 2003 Dec 9;61(11):1557-61. doi: 10.1212/01.wnl.0000095966.99430.f4. Neurology. 2003. PMID: 14663042
3,914 results