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Journal Abstract Search

360 related items for PubMed ID: 17469194

  • 1. 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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  • 3. 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 15; 63(3):377-82. PubMed ID: 16533964
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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 15; 15(4):277-80. PubMed ID: 18805725
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  • 5. Genetic screening for the LRRK2 R1441C and G2019S mutations in Parkinsonian patients from Campania.
    De Rosa A, De Michele G, Guacci A, Carbone R, Lieto M, Peluso S, Picillo M, Barone P, Salemi F, Laiso A, Saccà F, Tessitore A, Pellecchia MT, Bonifati V, Criscuolo C.
    J Parkinsons Dis; 2014 May 15; 4(1):123-8. PubMed ID: 24496098
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  • 6. 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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  • 9. [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 May 15; 111(12):56-62. PubMed ID: 22433811
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  • 10. 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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  • 12. Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2.
    Ruiz-Martínez J, de la Riva P, Rodríguez-Oroz MC, Mondragón Rezola E, Bergareche A, Gorostidi A, Gago B, Estanga A, Larrañaga N, Sarasqueta C, López de Munain A, Martí Massó JF.
    Mov Disord; 2014 May 15; 29(6):750-5. PubMed ID: 24357540
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  • 13. 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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  • 15. Low frequency of common LRRK2 mutations in Mexican patients with Parkinson's disease.
    Yescas P, López M, Monroy N, Boll MC, Rodríguez-Violante M, Rodríguez U, Ochoa A, Alonso ME.
    Neurosci Lett; 2010 Nov 19; 485(2):79-82. PubMed ID: 20727385
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  • 19. The prevalence of the G2019S and R1441C/G/H mutations in LRRK2 in German patients with Parkinson's disease.
    Möller JC, Rissling I, Mylius V, Höft C, Eggert KM, Oertel WH.
    Eur J Neurol; 2008 Jul 19; 15(7):743-5. PubMed ID: 18484993
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  • 20. Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population.
    Janković MZ, Kresojević ND, Dobričić VS, Marković VV, Petrović IN, Novaković IV, Kostić VS.
    J Neurol Sci; 2015 Jul 19; 353(1-2):59-62. PubMed ID: 25899316
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