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Journal Abstract Search

226 related items for PubMed ID: 10791092

  • 1. [Parkin gene and its function; a key to understand nigral degeneration].
    Hattori N, Mizuno Y.
    Rinsho Shinkeigaku; 1999 Dec; 39(12):1259-61. PubMed ID: 10791092
    [Abstract] [Full Text] [Related]

  • 2. Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.
    Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y.
    Ann Neurol; 1998 Dec; 44(6):935-41. PubMed ID: 9851438
    [Abstract] [Full Text] [Related]

  • 3. Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.
    Shimura H, Hattori N, Kubo S, Yoshikawa M, Kitada T, Matsumine H, Asakawa S, Minoshima S, Yamamura Y, Shimizu N, Mizuno Y.
    Ann Neurol; 1999 May; 45(5):668-72. PubMed ID: 10319893
    [Abstract] [Full Text] [Related]

  • 4. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N.
    Rinsho Shinkeigaku; 2004 May; 44(4-5):241-62. PubMed ID: 15287506
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  • 7. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
    Abbas N, Lücking CB, Ricard S, Dürr A, Bonifati V, De Michele G, Bouley S, Vaughan JR, Gasser T, Marconi R, Broussolle E, Brefel-Courbon C, Harhangi BS, Oostra BA, Fabrizio E, Böhme GA, Pradier L, Wood NW, Filla A, Meco G, Denefle P, Agid Y, Brice A.
    Hum Mol Genet; 1999 Apr; 8(4):567-74. PubMed ID: 10072423
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  • 9. Parkin-associated Parkinson's disease.
    von Coelln R, Dawson VL, Dawson TM.
    Cell Tissue Res; 2004 Oct; 318(1):175-84. PubMed ID: 15503153
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  • 10. Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease.
    Hattori N, Shimura H, Kubo S, Wang M, Shimizu N, Tanaka K, Mizuno Y.
    J Neural Transm Suppl; 2000 Oct; (60):101-16. PubMed ID: 11205133
    [Abstract] [Full Text] [Related]

  • 11. [Parkin gene: its mutations and function].
    Hattori N.
    Rinsho Shinkeigaku; 2002 Nov; 42(11):1077-81. PubMed ID: 12784670
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  • 12. [Two cases of sporadic juvenile Parkinson's disease caused by homozygous deletion of Parkin gene].
    Ujike H, Yamamoto M, Yamaguchi K, Kanzaki A, Takagi M, Kuroda S.
    No To Shinkei; 1999 Dec; 51(12):1061-4. PubMed ID: 10654303
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  • 13. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
    Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N.
    Nature; 1998 Apr 09; 392(6676):605-8. PubMed ID: 9560156
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  • 14. Parkin and Parkinson's disease.
    Mizuno Y, Hattori N, Mori H, Suzuki T, Tanaka K.
    Curr Opin Neurol; 2001 Aug 09; 14(4):477-82. PubMed ID: 11470964
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  • 15. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
    Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, Ben Hamida M, Hattori N, Mizuno Y, Hentati F.
    Parkinsonism Relat Disord; 2003 Jun 09; 9(5):247-51. PubMed ID: 12781588
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  • 16. Progress in the clinical and molecular genetics of familial parkinsonism.
    Kitada T, Asakawa S, Matsumine H, Hattori N, Shimura H, Minoshima S, Shimizu N, Mizuno Y.
    Neurogenetics; 2000 Mar 09; 2(4):207-18. PubMed ID: 10983716
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  • 18. Prevalence of parkin gene mutations and variations in idiopathic Parkinson's disease.
    Sinha R, Racette B, Perlmutter JS, Parsian A.
    Parkinsonism Relat Disord; 2005 Sep 09; 11(6):341-7. PubMed ID: 16019250
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  • 20. [A Parkin gene (PARK 2) and Parkinson's disease].
    Matsumine H.
    Rinsho Shinkeigaku; 1999 Jan 09; 39(1):9-12. PubMed ID: 10377786
    [Abstract] [Full Text] [Related]

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