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Journal Abstract Search

221 related items for PubMed ID: 26600626

  • 1. Analysis of the LRRK2 p.G2019S mutation in Colombian Parkinson's Disease Patients.
    Duque AF, Lopez JC, Benitez B, Hernandez H, Yunis JJ, Fernandez W, Arboleda H, Arboleda G.
    Colomb Med (Cali); 2015 Sep 30; 46(3):117-21. PubMed ID: 26600626
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  • 2. 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 30; 14(4):413-7. PubMed ID: 17388990
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  • 3. Frequency of LRRK2 mutations in early- and late-onset Parkinson disease.
    Clark LN, Wang Y, Karlins E, Saito L, Mejia-Santana H, Harris J, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, Ottman R, Marder K.
    Neurology; 2006 Nov 28; 67(10):1786-91. PubMed ID: 17050822
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  • 5. 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 28; 63(3):377-82. PubMed ID: 16533964
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  • 10. Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutation.
    Yahalom G, Kaplan N, Vituri A, Cohen OS, Inzelberg R, Kozlova E, Korczyn AD, Rosset S, Friedman E, Hassin-Baer S.
    Parkinsonism Relat Disord; 2012 Nov 28; 18(9):1039-41. PubMed ID: 22703868
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  • 12. 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 28; 64(3):425-30. PubMed ID: 17353388
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  • 14. LRRK2 mutations are a common cause of Parkinson's disease in Spain.
    Mata IF, Ross OA, Kachergus J, Huerta C, Ribacoba R, Moris G, Blazquez M, Guisasola LM, Salvador C, Martinez C, Farrer M, Alvarez V.
    Eur J Neurol; 2006 Apr 28; 13(4):391-4. PubMed ID: 16643318
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  • 15. A study of LRRK2 mutations and Parkinson's disease in Brazil.
    Pimentel MM, Moura KC, Abdalla CB, Pereira JS, de Rosso AL, Nicaretta DH, Campos M, de Almeida RM, dos Santos JM, Bastos IC, Mendes MF, Maultasch H, Costa FH, Werneck AL, Santos-Rebouças CB.
    Neurosci Lett; 2008 Mar 05; 433(1):17-21. PubMed ID: 18201824
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  • 19. Frequency of the LRRK2 G2019S mutation in late-onset sporadic patients with Parkinson's disease.
    Chien HF, Figueiredo TR, Hollaender MA, Tofoli F, Takada LT, Pereira Lda V, Barbosa ER.
    Arq Neuropsiquiatr; 2014 May 05; 72(5):356-9. PubMed ID: 24863511
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