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Journal Abstract Search

421 related items for PubMed ID: 17097110

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  • 2. LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.
    Gaig C, Ezquerra M, Marti MJ, Muñoz E, Valldeoriola F, Tolosa E.
    Arch Neurol; 2006 Mar; 63(3):377-82. PubMed ID: 16533964
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  • 3. 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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  • 4. 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 16; 15(4):277-80. PubMed ID: 18805725
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  • 10. High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal.
    Ferreira JJ, Guedes LC, Rosa MM, Coelho M, van Doeselaar M, Schweiger D, Di Fonzo A, Oostra BA, Sampaio C, Bonifati V.
    Mov Disord; 2007 Jun 15; 22(8):1194-201. PubMed ID: 17469194
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  • 12. 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 15; 21(12):2234-6. PubMed ID: 17044089
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  • 13. Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.
    Lee AJ, Wang Y, Alcalay RN, Mejia-Santana H, Saunders-Pullman R, Bressman S, Corvol JC, Brice A, Lesage S, Mangone G, Tolosa E, Pont-Sunyer C, Vilas D, Schüle B, Kausar F, Foroud T, Berg D, Brockmann K, Goldwurm S, Siri C, Asselta R, Ruiz-Martinez J, Mondragón E, Marras C, Ghate T, Giladi N, Mirelman A, Marder K, Michael J. Fox LRRK2 Cohort Consortium.
    Mov Disord; 2017 Oct 15; 32(10):1432-1438. PubMed ID: 28639421
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  • 14. G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
    Lesage S, Ibanez P, Lohmann E, Pollak P, Tison F, Tazir M, Leutenegger AL, Guimaraes J, Bonnet AM, Agid Y, Dürr A, Brice A, French Parkinson's Disease Genetics Study Group.
    Ann Neurol; 2005 Nov 15; 58(5):784-7. PubMed ID: 16240353
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  • 16. 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 Nov 15; 4(2-3):195-8. PubMed ID: 17596714
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  • 17. Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
    Ishihara L, Warren L, Gibson R, Amouri R, Lesage S, Dürr A, Tazir M, Wszolek ZK, Uitti RJ, Nichols WC, Griffith A, Hattori N, Leppert D, Watts R, Zabetian CP, Foroud TM, Farrer MJ, Brice A, Middleton L, Hentati F.
    Arch Neurol; 2006 Sep 15; 63(9):1250-4. PubMed ID: 16966502
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  • 19. [Clinical features of LRRK2-associated Parkinson's disease].
    Pchelina SN, Ivanova ON, Emel'ianov AK, Iakimovskiĭ AF.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2011 Sep 15; 111(12):56-62. PubMed ID: 22433811
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