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Pubmed for Handhelds

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Journal Abstract Search

357 related items for PubMed ID: 12730996

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  • 23. Early-onset Parkinson's disease caused by a novel parkin mutation in a genetic isolate from north-eastern Brazil.
    Chien HF, Rohé CF, Costa MD, Breedveld GJ, Oostra BA, Barbosa ER, Bonifati V.
    Neurogenetics; 2006 Mar; 7(1):13-9. PubMed ID: 16328510
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  • 26. Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients.
    Bognar C, Baldovic M, Benetin J, Kadasi L, Zatkova A.
    Gen Physiol Biophys; 2013 Mar; 32(1):55-66. PubMed ID: 23531835
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  • 28. Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations.
    Hedrich K, Marder K, Harris J, Kann M, Lynch T, Meija-Santana H, Pramstaller PP, Schwinger E, Bressman SB, Fahn S, Klein C.
    Neurology; 2002 Apr 23; 58(8):1239-46. PubMed ID: 11971093
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  • 29. Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.
    Lücking CB, Chesneau V, Lohmann E, Verpillat P, Dulac C, Bonnet AM, Gasparini F, Agid Y, Dürr A, Brice A.
    Arch Neurol; 2003 Sep 23; 60(9):1253-6. PubMed ID: 12975291
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  • 30. Parkin mutations are frequent in patients with isolated early-onset parkinsonism.
    Periquet M, Latouche M, Lohmann E, Rawal N, De Michele G, Ricard S, Teive H, Fraix V, Vidailhet M, Nicholl D, Barone P, Wood NW, Raskin S, Deleuze JF, Agid Y, Dürr A, Brice A, French Parkinson's Disease Genetics Study Group, European Consortium on Genetic Susceptibility in Parkinson's Disease.
    Brain; 2003 Jun 23; 126(Pt 6):1271-8. PubMed ID: 12764050
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  • 31. parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.
    Poorkaj P, Nutt JG, James D, Gancher S, Bird TD, Steinbart E, Schellenberg GD, Payami H.
    Am J Med Genet A; 2004 Aug 15; 129A(1):44-50. PubMed ID: 15266615
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  • 33. 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 15; 50(3):293-300. PubMed ID: 11558785
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  • 34. Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control.
    Brooks J, Ding J, Simon-Sanchez J, Paisan-Ruiz C, Singleton AB, Scholz SW.
    J Med Genet; 2009 Jun 15; 46(6):375-81. PubMed ID: 19351622
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  • 38. The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
    Bonifati V, De Michele G, Lücking CB, Dürr A, Fabrizio E, Ambrosio G, Vanacore N, De Mari M, Marconi R, Capus L, Breteler MM, Gasser T, Oostra B, Wood N, Agid Y, Filla A, Meco G, Brice A, Italian PD Genetics Study Group, French PD Genetics Study Group, European Consortium on Genetic Susceptibility in PD.
    Neurol Sci; 2001 Feb 15; 22(1):51-2. PubMed ID: 11487197
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