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Page 1
Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease.
Brockmann K, Schulte C, Schneiderhan-Marra N, Apel A, Pont-Sunyer C, Vilas D, Ruiz-Martinez J, Langkamp M, Corvol JC, Cormier F, Knorpp T, Joos TO, Bernard A, Gasser T, Marras C, Schüle B, Aasly JO, Foroud T, Marti-Masso JF, Brice A, Tolosa E, Berg D, Maetzler W. Brockmann K, et al. Among authors: corvol jc. Eur J Neurol. 2017 Feb;24(2):427-e6. doi: 10.1111/ene.13223. Eur J Neurol. 2017. PMID: 28102045
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism.
Klebe S, Golmard JL, Nalls MA, Saad M, Singleton AB, Bras JM, Hardy J, Simon-Sanchez J, Heutink P, Kuhlenbäumer G, Charfi R, Klein C, Hagenah J, Gasser T, Wurster I, Lesage S, Lorenz D, Deuschl G, Durif F, Pollak P, Damier P, Tison F, Durr A, Amouyel P, Lambert JC, Tzourio C, Maubaret C, Charbonnier-Beaupel F, Tahiri K, Vidailhet M, Martinez M, Brice A, Corvol JC; French Parkinson's Disease Genetics Study Group; International Parkinson's Disease Genomics Consortium (IPDGC). Klebe S, et al. Among authors: corvol jc. J Neurol Neurosurg Psychiatry. 2013 Jun;84(6):666-73. doi: 10.1136/jnnp-2012-304475. Epub 2013 Feb 13. J Neurol Neurosurg Psychiatry. 2013. PMID: 23408064 Free PMC article.
Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's.
Liu G, Boot B, Locascio JJ, Jansen IE, Winder-Rhodes S, Eberly S, Elbaz A, Brice A, Ravina B, van Hilten JJ, Cormier-Dequaire F, Corvol JC, Barker RA, Heutink P, Marinus J, Williams-Gray CH, Scherzer CR; International Genetics of Parkinson Disease Progression (IGPP) Consortium. Liu G, et al. Among authors: corvol jc. Ann Neurol. 2016 Nov;80(5):674-685. doi: 10.1002/ana.24781. Ann Neurol. 2016. PMID: 27717005 Free PMC article.
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?
Lesage S, Condroyer C, Klebe S, Lohmann E, Durif F, Damier P, Tison F, Anheim M, Honoré A, Viallet F, Bonnet AM, Ouvrard-Hernandez AM, Vidailhet M, Durr A, Brice A; French Parkinson's Disease Genetics Study Group. Lesage S, et al. Neurobiol Aging. 2012 Sep;33(9):2233.e1-2233.e5. doi: 10.1016/j.neurobiolaging.2012.05.006. Epub 2012 Jun 1. Neurobiol Aging. 2012. PMID: 22658323 Free article.
"De-novo" consultation: Evaluation of an outpatient's clinic dedicated to early diagnosis of parkinsonian syndromes.
Ruggeri J, Mariani LL, Aix S, Bonnet AM, Cormier F, Corvol JC, Dodet P, Grabli D, Hartmann A, Hubsch C, Lacomblez L, Roze E, Welter ML, Worbe Y, Vidailhet M, Degos B. Ruggeri J, et al. Among authors: corvol jc. Rev Neurol (Paris). 2017 Jan-Feb;173(1-2):55-61. doi: 10.1016/j.neurol.2016.12.031. Epub 2017 Jan 31. Rev Neurol (Paris). 2017. PMID: 28159316
The PINK1 kinase-driven ubiquitin ligase Parkin promotes mitochondrial protein import through the presequence pathway in living cells.
Jacoupy M, Hamon-Keromen E, Ordureau A, Erpapazoglou Z, Coge F, Corvol JC, Nosjean O, Mannoury la Cour C, Millan MJ, Boutin JA, Harper JW, Brice A, Guedin D, Gautier CA, Corti O. Jacoupy M, et al. Among authors: corvol jc. Sci Rep. 2019 Aug 14;9(1):11829. doi: 10.1038/s41598-019-47352-9. Sci Rep. 2019. PMID: 31413265 Free PMC article.
Clinical implications of neuropharmacogenetics.
Corvol JC, Devos D, Hulot JS, Lacomblez L. Corvol JC, et al. Rev Neurol (Paris). 2015 Jun-Jul;171(6-7):482-97. doi: 10.1016/j.neurol.2015.04.003. Epub 2015 May 23. Rev Neurol (Paris). 2015. PMID: 26008819 Review.
360 results