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Journal Abstract Search

380 related items for PubMed ID: 27085187

  • 21. [Parkinson's disease: what have we learned from the genes responsible for familial forms?].
    Corti O, Brice A.
    Med Sci (Paris); 2003 May; 19(5):613-9. PubMed ID: 12836396
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  • 24. Alpha-synuclein pathology in Parkinson's and Alzheimer's disease brain: incidence and topographic distribution--a pilot study.
    Jellinger KA.
    Acta Neuropathol; 2003 Sep; 106(3):191-201. PubMed ID: 12845452
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  • 27. Lewy bodies and parkinsonism in families with parkin mutations.
    Farrer M, Chan P, Chen R, Tan L, Lincoln S, Hernandez D, Forno L, Gwinn-Hardy K, Petrucelli L, Hussey J, Singleton A, Tanner C, Hardy J, Langston JW.
    Ann Neurol; 2001 Sep; 50(3):293-300. PubMed ID: 11558785
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  • 32. Accelerated in vitro fibril formation by a mutant alpha-synuclein linked to early-onset Parkinson disease.
    Conway KA, Harper JD, Lansbury PT.
    Nat Med; 1998 Nov; 4(11):1318-20. PubMed ID: 9809558
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  • 33. DJ-1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7.
    Di Nottia M, Masciullo M, Verrigni D, Petrillo S, Modoni A, Rizzo V, Di Giuda D, Rizza T, Niceta M, Torraco A, Bianchi M, Santoro M, Bentivoglio AR, Bertini E, Piemonte F, Carrozzo R, Silvestri G.
    Clin Genet; 2017 Jul; 92(1):18-25. PubMed ID: 27460976
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  • 36. Familial parkinsonism, dementia, and Lewy body disease: study of family G.
    Denson MA, Wszolek ZK, Pfeiffer RF, Wszolek EK, Paschall TM, McComb RD.
    Ann Neurol; 1997 Oct; 42(4):638-43. PubMed ID: 9382476
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  • 37. A stable proportion of Lewy body bearing neurons in the substantia nigra suggests a model in which the Lewy body causes neuronal death.
    Greffard S, Verny M, Bonnet AM, Seilhean D, Hauw JJ, Duyckaerts C.
    Neurobiol Aging; 2010 Jan; 31(1):99-103. PubMed ID: 18457903
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  • 40. Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.
    Wilson GR, Sim JC, McLean C, Giannandrea M, Galea CA, Riseley JR, Stephenson SE, Fitzpatrick E, Haas SA, Pope K, Hogan KJ, Gregg RG, Bromhead CJ, Wargowski DS, Lawrence CH, James PA, Churchyard A, Gao Y, Phelan DG, Gillies G, Salce N, Stanford L, Marsh AP, Mignogna ML, Hayflick SJ, Leventer RJ, Delatycki MB, Mellick GD, Kalscheuer VM, D'Adamo P, Bahlo M, Amor DJ, Lockhart PJ.
    Am J Hum Genet; 2014 Dec 04; 95(6):729-35. PubMed ID: 25434005
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