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224 related items for PubMed ID: 12882651

  • 1. A linkage study of candidate loci in familial Parkinson's Disease.
    Wirdefeldt K, Burgess CE, Westerberg L, Payami H, Schalling M.
    BMC Neurol; 2003 Jul 26; 3():6. PubMed ID: 12882651
    [Abstract] [Full Text] [Related]

  • 2. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N.
    Rinsho Shinkeigaku; 2004 Jul 26; 44(4-5):241-62. PubMed ID: 15287506
    [Abstract] [Full Text] [Related]

  • 3. [A 73-year-old woman with familial Parkinson's disease].
    Takanashi M, Urabe T, Ohta S, Hamano Y, Mori H, Shirai T, Kondo T, Mizuno Y.
    No To Shinkei; 1999 Dec 26; 51(12):1087-96. PubMed ID: 10654309
    [Abstract] [Full Text] [Related]

  • 4. Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes.
    Gasser T, Wszolek ZK, Trofatter J, Ozelius L, Uitti RJ, Lee CS, Gusella J, Pfeiffer RF, Calne DB, Breakefield XO.
    Ann Neurol; 1994 Sep 26; 36(3):387-96. PubMed ID: 7915897
    [Abstract] [Full Text] [Related]

  • 5. The dopamine transporter protein gene (SLC6A3): primary linkage mapping and linkage studies in Tourette syndrome.
    Gelernter J, Vandenbergh D, Kruger SD, Pauls DL, Kurlan R, Pakstis AJ, Kidd KK, Uhl G.
    Genomics; 1995 Dec 10; 30(3):459-63. PubMed ID: 8825631
    [Abstract] [Full Text] [Related]

  • 6. Dopamine transporter density measured by [123I]beta-CIT single-photon emission computed tomography is normal in dopa-responsive dystonia.
    Jeon BS, Jeong JM, Park SS, Kim JM, Chang YS, Song HC, Kim KM, Yoon KY, Lee MC, Lee SB.
    Ann Neurol; 1998 Jun 10; 43(6):792-800. PubMed ID: 9629849
    [Abstract] [Full Text] [Related]

  • 7. Heredity in Parkinson's disease: new findings.
    Lev N, Melamed E.
    Isr Med Assoc J; 2001 Jun 10; 3(6):435-8. PubMed ID: 11433638
    [Abstract] [Full Text] [Related]

  • 8. Genetics of Parkinson's disease.
    Mizuno Y, Hattori N, Mori H.
    Biomed Pharmacother; 1999 Apr 10; 53(3):109-16. PubMed ID: 10349506
    [Abstract] [Full Text] [Related]

  • 9. Linkage exclusion in French families with probable Parkinson' s disease.
    Farrer M, Destée T, Becquet E, Wavrant-De Vrièze F, Mouroux V, Richard F, Defebvre L, Lincoln S, Hardy J, Amouyel P, Chartier-Harlin MC.
    Mov Disord; 2000 Nov 10; 15(6):1075-83. PubMed ID: 11104189
    [Abstract] [Full Text] [Related]

  • 10. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
    Mineharu Y, Inoue K, Inoue S, Yamada S, Nozaki K, Hashimoto N, Koizumi A.
    Stroke; 2007 Apr 10; 38(4):1174-8. PubMed ID: 17322081
    [Abstract] [Full Text] [Related]

  • 11. Genetics of Parkinson's disease and essential tremor.
    Zimprich A.
    Curr Opin Neurol; 2011 Aug 10; 24(4):318-23. PubMed ID: 21734494
    [Abstract] [Full Text] [Related]

  • 12. Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.
    Panhuysen CI, Karban A, Knodle Manning A, Bayless TM, Duerr RH, Bailey-Wilson JE, Epstein EH, Brant SR.
    Hum Genet; 2006 Aug 10; 120(1):31-41. PubMed ID: 16733713
    [Abstract] [Full Text] [Related]

  • 13. A susceptibility locus for Parkinson's disease maps to chromosome 2p13.
    Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, Bereznai B, Fabrizio E, Vieregge P, Horstmann RD.
    Nat Genet; 1998 Mar 10; 18(3):262-5. PubMed ID: 9500549
    [Abstract] [Full Text] [Related]

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  • 16. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations.
    Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T, Parkinson Study Group.
    Am J Hum Genet; 2002 Jul 10; 71(1):124-35. PubMed ID: 12058349
    [Abstract] [Full Text] [Related]

  • 17. Genetic heterogeneity in autosomal dominant essential tremor.
    Kovach MJ, Ruiz J, Kimonis K, Mueed S, Sinha S, Higgins C, Elble S, Elble R, Kimonis VE.
    Genet Med; 2001 Jul 10; 3(3):197-9. PubMed ID: 11388761
    [Abstract] [Full Text] [Related]

  • 18. Genetic analysis of synphilin-1 in familial Parkinson's disease.
    Farrer M, Destée A, Levecque C, Singleton A, Engelender S, Becquet E, Mouroux V, Richard F, Defebvre L, Crook R, Hernandez D, Ross CA, Hardy J, Amouyel P, Chartier-Harlin MC.
    Neurobiol Dis; 2001 Apr 10; 8(2):317-23. PubMed ID: 11300726
    [Abstract] [Full Text] [Related]

  • 19. A linkage study between bipolar disorder and genes involved in dopaminergic and GABAergic neurotransmission.
    De bruyn A, Souery D, Mendelbaum K, Mendlewicz J, Van Broeckhoven C.
    Psychiatr Genet; 1996 Apr 10; 6(2):67-73. PubMed ID: 8840392
    [Abstract] [Full Text] [Related]

  • 20. Autosomal-dominantly inherited forms of Parkinson's disease.
    Gasser T.
    J Neural Transm Suppl; 2000 Apr 10; (58):31-40. PubMed ID: 11128611
    [Abstract] [Full Text] [Related]

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