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Pubmed for Handhelds

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Journal Abstract Search

327 related items for PubMed ID: 16966502

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  • 3. G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia.
    Pchelina SN, Yakimovskii AF, Ivanova ON, Emelianov AK, Zakharchuk AH, Schwarzman AL.
    Mov Disord; 2006 Dec; 21(12):2234-6. PubMed ID: 17044089
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  • 4. Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.
    Lesage S, Leclere L, Lohmann E, Borg M, Ruberg M, Dürr A, Brice A, French Parkinson's Disease Genetics Study Group.
    Neurodegener Dis; 2007 Dec; 4(2-3):195-8. PubMed ID: 17596714
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  • 7. LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.
    Lesage S, Janin S, Lohmann E, Leutenegger AL, Leclere L, Viallet F, Pollak P, Durif F, Thobois S, Layet V, Vidailhet M, Agid Y, Dürr A, Brice A, French Parkinson's Disease Genetics Study Group, Bonnet AM, Borg M, Broussolle E, Damier P, Destée A, Martinez M, Penet C, Rasco O, Tison F, Tranchan C, Vérin M.
    Arch Neurol; 2007 Mar; 64(3):425-30. PubMed ID: 17353388
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  • 8. Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients.
    Floris G, Cannas A, Solla P, Murru MR, Tranquilli S, Corongiu D, Rolesu M, Cuccu S, Sardu C, Marrosu F, Marrosu MG.
    Parkinsonism Relat Disord; 2009 May; 15(4):277-80. PubMed ID: 18805725
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  • 9. Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease.
    Huang Y, Halliday GM, Vandebona H, Mellick GD, Mastaglia F, Stevens J, Kwok J, Garlepp M, Silburn PA, Horne MK, Kotschet K, Venn A, Rowe DB, Rubio JP, Sue CM.
    Mov Disord; 2007 May 15; 22(7):982-9. PubMed ID: 17427941
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  • 12. Genetic screening for LRRK2 gene G2019S mutation in Parkinson's disease patients from Southern Italy.
    De Rosa A, Criscuolo C, Mancini P, De Martino M, Giordano IA, Pappatà S, Filla A, De Michele G.
    Parkinsonism Relat Disord; 2009 Mar 15; 15(3):242-4. PubMed ID: 18621566
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  • 13. A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia.
    Illarioshkin SN, Shadrina MI, Slominsky PA, Bespalova EV, Zagorovskaya TB, Bagyeva GKh, Markova ED, Limborska SA, Ivanova-Smolenskaya IA.
    Eur J Neurol; 2007 Apr 15; 14(4):413-7. PubMed ID: 17388990
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  • 15. The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?
    Orr-Urtreger A, Shifrin C, Rozovski U, Rosner S, Bercovich D, Gurevich T, Yagev-More H, Bar-Shira A, Giladi N.
    Neurology; 2007 Oct 16; 69(16):1595-602. PubMed ID: 17938369
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  • 20. LRRK2 gene in Parkinson disease: mutation analysis and case control association study.
    Paisán-Ruíz C, Lang AE, Kawarai T, Sato C, Salehi-Rad S, Fisman GK, Al-Khairallah T, St George-Hyslop P, Singleton A, Rogaeva E.
    Neurology; 2005 Sep 13; 65(5):696-700. PubMed ID: 16157901
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