These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

129 related items for PubMed ID: 18591135

  • 1. Positional cloning of the autosomal recessive juvenile parkinsonism (AR-JP) gene and its diversity in deletion mutations.
    Kitada T, Asakawa S, Matsumine H, Hattori N, Minoshima S, Shimizu N, Mizuno Y.
    Parkinsonism Relat Disord; 1999 Dec; 5(4):163-8. PubMed ID: 18591135
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. 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]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. 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; 9(5):247-51. PubMed ID: 12781588
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. A homozygous parkin p.G284R mutation in a Chinese family with autosomal recessive juvenile parkinsonism.
    Chen H, Huang X, Yuan L, Xia H, Xu H, Yang Y, Zheng W, Deng H.
    Neurosci Lett; 2016 Jun 15; 624():100-4. PubMed ID: 27177722
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 8(4):567-74. PubMed ID: 10072423
    [Abstract] [Full Text] [Related]

  • 13. [Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease].
    Hattori N.
    Rinsho Shinkeigaku; 2004 Apr 15; 44(4-5):241-62. PubMed ID: 15287506
    [Abstract] [Full Text] [Related]

  • 14. Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium.
    Saito M, Matsumine H, Tanaka H, Ishikawa A, Shimoda-Matsubayashi S, Schäffer AA, Mizuno Y, Tsuji S.
    J Hum Genet; 1998 Apr 15; 43(1):22-31. PubMed ID: 9609994
    [Abstract] [Full Text] [Related]

  • 15. Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's Disease.
    Tassin J, Dürr A, de Broucker T, Abbas N, Bonifati V, De Michele G, Bonnet AM, Broussolle E, Pollak P, Vidailhet M, De Mari M, Marconi R, Medjbeur S, Filla A, Meco G, Agid Y, Brice A.
    Am J Hum Genet; 1998 Jul 15; 63(1):88-94. PubMed ID: 9634531
    [Abstract] [Full Text] [Related]

  • 16. PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.
    Shimizu N, Asakawa S, Minoshima S, Kitada T, Hattori N, Matsumine H, Yokochi M, Yamamura Y, Mizuno Y.
    J Neural Transm Suppl; 2000 Jul 15; (58):19-30. PubMed ID: 11128608
    [Abstract] [Full Text] [Related]

  • 17. Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism.
    Illarioshkin SN, Periquet M, Rawal N, Lücking CB, Zagorovskaya TB, Slominsky PA, Miloserdova OV, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, Brice A.
    Mov Disord; 2003 Aug 15; 18(8):914-9. PubMed ID: 12889082
    [Abstract] [Full Text] [Related]

  • 18. Homozygous deletion mutation of the parkin gene in patients with atypical parkinsonism.
    Kuroda Y, Mitsui T, Akaike M, Azuma H, Matsumoto T.
    J Neurol Neurosurg Psychiatry; 2001 Aug 15; 71(2):231-4. PubMed ID: 11459900
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.