Marras C - Search Results

1

Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.

Lee AJ, Wang Y, Alcalay RN, Mejia-Santana H, Saunders-Pullman R, Bressman S, Corvol JC, Brice A, Lesage S, Mangone G, Tolosa E, Pont-Sunyer C, Vilas D, Schüle B, Kausar F, Foroud T, Berg D, Brockmann K, Goldwurm S, Siri C, Asselta R, Ruiz-Martinez J, Mondragón E, Marras C, Ghate T, Giladi N, Mirelman A, Marder K; Michael J. Fox LRRK2 Cohort Consortium. Lee AJ, et al. Among authors: marras c. Mov Disord. 2017 Oct;32(10):1432-1438. doi: 10.1002/mds.27059. Epub 2017 Jun 22. Mov Disord. 2017. PMID: 28639421 Free PMC article.

2

Smell identification ability in twin pairs discordant for Parkinson's disease.

Marras C, Goldman S, Smith A, Barney P, Aston D, Comyns K, Korell M, Langston JW, Ross GW, Tanner CM. Marras C, et al. Mov Disord. 2005 Jun;20(6):687-93. doi: 10.1002/mds.20389. Mov Disord. 2005. PMID: 15719425

3

Antipsychotic use in older adults with Parkinson's disease.

Marras C, Kopp A, Qiu F, Lang AE, Sykora K, Shulman KI, Rochon PA. Marras C, et al. Mov Disord. 2007 Feb 15;22(3):319-23. doi: 10.1002/mds.21192. Mov Disord. 2007. PMID: 17149718

4

The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: phenotype in monozygotic twins.

Munhoz RP, Wakutani Y, Marras C, Teive HA, Raskin S, Werneck LC, Moreno D, Sato C, Lang AE, Rogaeva E. Munhoz RP, et al. Among authors: marras c. Mov Disord. 2008 Jan 30;23(2):290-4. doi: 10.1002/mds.21832. Mov Disord. 2008. PMID: 17999435

5

A comparison of the mini mental state exam to the Montreal cognitive assessment in identifying cognitive deficits in Parkinson's disease.

Zadikoff C, Fox SH, Tang-Wai DF, Thomsen T, de Bie RM, Wadia P, Miyasaki J, Duff-Canning S, Lang AE, Marras C. Zadikoff C, et al. Among authors: marras c. Mov Disord. 2008 Jan 30;23(2):297-9. doi: 10.1002/mds.21837. Mov Disord. 2008. PMID: 18044697

6

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.

Healy DG, Falchi M, O'Sullivan SS, Bonifati V, Durr A, Bressman S, Brice A, Aasly J, Zabetian CP, Goldwurm S, Ferreira JJ, Tolosa E, Kay DM, Klein C, Williams DR, Marras C, Lang AE, Wszolek ZK, Berciano J, Schapira AH, Lynch T, Bhatia KP, Gasser T, Lees AJ, Wood NW; International LRRK2 Consortium. Healy DG, et al. Among authors: marras c. Lancet Neurol. 2008 Jul;7(7):583-90. doi: 10.1016/S1474-4422(08)70117-0. Epub 2008 Jun 6. Lancet Neurol. 2008. PMID: 18539534 Free PMC article.

7

LRRK2 and Parkin mutations in a family with parkinsonism-Lack of genotype-phenotype correlation.

Marras C, Klein C, Lang AE, Wakutani Y, Moreno D, Sato C, Yip E, Munhoz RP, Lohmann K, Djarmati A, Bi A, Rogaeva E. Marras C, et al. Neurobiol Aging. 2010 Apr;31(4):721-2. doi: 10.1016/j.neurobiolaging.2008.05.030. Epub 2008 Jul 21. Neurobiol Aging. 2010. PMID: 18644660

8

A comparison of treatment thresholds in two large Parkinson's disease clinical trial cohorts.

Marras C, Lang AE, Eberly SW, Oakes D, Fahn S, Schwid SR, Hyson C, Shoulson I; Parkinson Study Group DATATOP and PRECEPT investigators. Marras C, et al. Mov Disord. 2009 Dec 15;24(16):2370-8. doi: 10.1002/mds.22828. Mov Disord. 2009. PMID: 19908310 Clinical Trial.

9

Predictors of time to requiring dopaminergic treatment in 2 Parkinson's disease cohorts.

Marras C, McDermott MP, Marek K, Rochon P, Naglie G, Tanner CM, Rudolph A, Shoulson I, Lang AE; Parkinson Study Group DATATOP and PRECEPT investigators. Marras C, et al. Mov Disord. 2011 Mar;26(4):608-13. doi: 10.1002/mds.23581. Epub 2011 Feb 1. Mov Disord. 2011. PMID: 21287602

10

The curious case of phenocopies in families with genetic Parkinson's disease.

Klein C, Chuang R, Marras C, Lang AE. Klein C, et al. Among authors: marras c. Mov Disord. 2011 Aug 15;26(10):1793-802. doi: 10.1002/mds.23853. Epub 2011 Jul 6. Mov Disord. 2011. PMID: 21735483 Review.

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