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Case-control study of the parkin gene in early-onset Parkinson disease.
Clark LN, Afridi S, Karlins E, Wang Y, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Clark LN, et al. Among authors: cote lj. Arch Neurol. 2006 Apr;63(4):548-52. doi: 10.1001/archneur.63.4.548. Arch Neurol. 2006. PMID: 16606767 Free article.
Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study.
Alcalay RN, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Ross BM, Verbitsky M, Kisselev S, Louis ED, Comella C, Colcher A, Jennings D, Nance MA, Bressman SB, Scott WK, Tanner C, Mickel S, Andrews H, Waters C, Fahn S, Cote L, Frucht S, Ford B, Rezak M, Novak K, Friedman JH, Pfeiffer R, Marsh L, Hiner B, Siderowf A, Ottman R, Marder K, Clark LN. Alcalay RN, et al. Arch Neurol. 2010 Sep;67(9):1116-22. doi: 10.1001/archneurol.2010.194. Arch Neurol. 2010. PMID: 20837857 Free PMC article.
The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
Sharp ME, Caccappolo E, Mejia-Santana H, Tang MX, Rosado L, Orbe Reilly M, Ruiz D, Louis ED, Comella C, Nance M, Bressman S, Scott WK, Tanner C, Waters C, Fahn S, Cote L, Ford B, Rezak M, Novak K, Friedman JH, Pfeiffer R, Payami H, Molho E, Factor SA, Nutt J, Serrano C, Arroyo M, Pauciulo MW, Nichols WC, Clark LN, Alcalay RN, Marder KS. Sharp ME, et al. Mov Disord. 2015 Feb;30(2):278-83. doi: 10.1002/mds.26065. Epub 2014 Nov 12. Mov Disord. 2015. PMID: 25393808 Free PMC article.
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations.
Clark LN, Afridi S, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Singleton A, Wavrant De-Vrieze F, Hardy J, Mayeux R, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K. Clark LN, et al. Among authors: cote lj. Mov Disord. 2004 Jul;19(7):796-800. doi: 10.1002/mds.20131. Mov Disord. 2004. PMID: 15254937
95 results