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Journal Abstract Search

116 related items for PubMed ID: 1922124

  • 1. A clinical and genetic study of familial Parkinson's disease.
    Maraganore DM, Harding AE, Marsden CD.
    Mov Disord; 1991; 6(3):205-11. PubMed ID: 1922124
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  • 2. 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; 18(3):262-5. PubMed ID: 9500549
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  • 3. Clinical features of familial Parkinson's disease in Thai patients.
    Prueksaritanond S, Boongird P, Pulkes T, Prueksaritanond S.
    Qual Prim Care; 2009 Mar; 17(2):115-22. PubMed ID: 19416604
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  • 4. Study of familial Parkinson's disease in Russia, Uzbekistan, and Zambia.
    Atadzhanov M, Zumla A, Mwaba P.
    Postgrad Med J; 2005 Feb; 81(952):117-21. PubMed ID: 15701745
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  • 5. [Incidence and clinical profile of familial forms of Parkinson's disease. A study of 428 index-cases from a department of neurology].
    Broussolle E, Defuentes G, Plauchu H, Chazot G.
    Rev Neurol (Paris); 1997 Jul; 153(6-7):406-11. PubMed ID: 9684007
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  • 6. Complex segregation analysis of Parkinson's disease: The Mayo Clinic Family Study.
    McDonnell SK, Schaid DJ, Elbaz A, Strain KJ, Bower JH, Ahlskog JE, Maraganore DM, Rocca WA.
    Ann Neurol; 2006 May; 59(5):788-95. PubMed ID: 16634030
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  • 7. Genetic basis of common diseases: the general theory of Mendelian recessive genetics.
    Hutchinson M, Spanaki C, Lebedev S, Plaitakis A.
    Med Hypotheses; 2005 May; 65(2):282-6. PubMed ID: 15922101
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  • 8. Genetic susceptibility to Parkinson's disease.
    Johnson WG.
    Geriatrics; 1991 Aug; 46 Suppl 1():52-9. PubMed ID: 1894147
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  • 11. A large kindred with autosomal dominant Parkinson's disease.
    Golbe LI, Di Iorio G, Bonavita V, Miller DC, Duvoisin RC.
    Ann Neurol; 1990 Mar; 27(3):276-82. PubMed ID: 2158268
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  • 14. GIGYF2 mutations are not a frequent cause of familial Parkinson's disease.
    Di Fonzo A, Fabrizio E, Thomas A, Fincati E, Marconi R, Tinazzi M, Breedveld GJ, Simons EJ, Chien HF, Ferreira JJ, Horstink MW, Abbruzzese G, Borroni B, Cossu G, Dalla Libera A, Fabbrini G, Guidi M, De Mari M, Lopiano L, Martignoni E, Marini P, Onofrj M, Padovani A, Stocchi F, Toni V, Sampaio C, Barbosa ER, Meco G, Italian Parkinson Genetics Network, Oostra BA, Bonifati V.
    Parkinsonism Relat Disord; 2009 Nov; 15(9):703-5. PubMed ID: 19482505
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  • 16. Familial antiphospholipid antibody syndrome: criteria for disease and evidence for autosomal dominant inheritance.
    Goel N, Ortel TL, Bali D, Anderson JP, Gourley IS, Smith H, Morris CA, DeSimone M, Branch DW, Ford P, Berdeaux D, Roubey RA, Kostyu DD, Kingsmore SF, Thiel T, Amos C, Seldin MF.
    Arthritis Rheum; 1999 Feb; 42(2):318-27. PubMed ID: 10025927
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  • 18. Pathogenesis of familial Parkinson's disease: new insights based on monogenic forms of Parkinson's disease.
    Hatano T, Kubo S, Sato S, Hattori N.
    J Neurochem; 2009 Dec; 111(5):1075-93. PubMed ID: 19780902
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