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Journal Abstract Search

330 related items for PubMed ID: 17846414

  • 21. Phenotypic commonalities in familial and sporadic Parkinson disease.
    Baba Y, Markopoulou K, Putzke JD, Whaley NR, Farrer MJ, Wszolek ZK, Uitti RJ.
    Arch Neurol; 2006 Apr; 63(4):579-83. PubMed ID: 16606772
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  • 23. Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.
    Huerta C, Castro MG, Coto E, Blázquez M, Ribacoba R, Guisasola LM, Salvador C, Martínez C, Lahoz CH, Alvarez V.
    J Neurol Sci; 2005 Sep 15; 236(1-2):49-54. PubMed ID: 15975594
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  • 26. PITX3 polymorphism is associated with early onset Parkinson's disease.
    Bergman O, Håkansson A, Westberg L, Nordenström K, Carmine Belin A, Sydow O, Olson L, Holmberg B, Eriksson E, Nissbrandt H.
    Neurobiol Aging; 2010 Jan 15; 31(1):114-7. PubMed ID: 18420308
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  • 27. Mitochondrial DNA polymerase gamma mutations: an ever expanding molecular and clinical spectrum.
    Tang S, Wang J, Lee NC, Milone M, Halberg MC, Schmitt ES, Craigen WJ, Zhang W, Wong LJ.
    J Med Genet; 2011 Oct 15; 48(10):669-81. PubMed ID: 21880868
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  • 29. Assessment of PINK1 (PARK6) polymorphisms in Finnish PD.
    Clarimón J, Eerola J, Hellström O, Peuralinna T, Tienari PJ, Singleton AB.
    Neurobiol Aging; 2006 Jun 15; 27(6):906-7. PubMed ID: 16046032
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  • 30. Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population.
    Myhre R, Toft M, Kachergus J, Hulihan MM, Aasly JO, Klungland H, Farrer MJ.
    Acta Neurol Scand; 2008 Nov 15; 118(5):320-7. PubMed ID: 18485051
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  • 31. Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.
    Pyle A, Foltynie T, Tiangyou W, Lambert C, Keers SM, Allcock LM, Davison J, Lewis SJ, Perry RH, Barker R, Burn DJ, Chinnery PF.
    Ann Neurol; 2005 Apr 15; 57(4):564-7. PubMed ID: 15786469
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  • 33. Association of the hOGG1 Ser326Cys polymorphism with sporadic amyotrophic lateral sclerosis.
    Coppedè F, Mancuso M, Lo Gerfo A, Carlesi C, Piazza S, Rocchi A, Petrozzi L, Nesti C, Micheli D, Bacci A, Migliore L, Murri L, Siciliano G.
    Neurosci Lett; 2007 Jun 13; 420(2):163-8. PubMed ID: 17531381
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  • 34. Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany.
    Lücking CB, Lichtner P, Kramer ER, Gieger C, Illig T, Dichgans M, Berg D, Gasser T.
    Neurobiol Aging; 2010 Jan 13; 31(1):167-8. PubMed ID: 18436345
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  • 35. The transcription factor PITX3 is associated with sporadic Parkinson's disease.
    Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, Wüllner U, Illig T, Sharma M, Gasser T.
    Neurobiol Aging; 2009 May 13; 30(5):731-8. PubMed ID: 17905480
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  • 36. Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome.
    Luoma PT, Luo N, Löscher WN, Farr CL, Horvath R, Wanschitz J, Kiechl S, Kaguni LS, Suomalainen A.
    Hum Mol Genet; 2005 Jul 15; 14(14):1907-20. PubMed ID: 15917273
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  • 39. Is the CAG repeat of mitochondrial DNA polymerase gamma (POLG) associated with male infertility? A multi-centre French study.
    Aknin-Seifer IE, Touraine RL, Lejeune H, Jimenez C, Chouteau J, Siffroi JP, McElreavey K, Bienvenu T, Patrat C, Levy R.
    Hum Reprod; 2005 Mar 15; 20(3):736-40. PubMed ID: 15650046
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