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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 12013904

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  • 2. Hereditary spastic paraplegia: the pace quickens.
    Fink JK.
    Ann Neurol; 2002 Jun; 51(6):669-72. PubMed ID: 12112070
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  • 7. Hereditary spastic paraplegia.
    McDermott CJ, Shaw PJ.
    Int Rev Neurobiol; 2002 Jun; 53():191-204. PubMed ID: 12512341
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  • 8. Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia.
    McCorquodale DS, Ozomaro U, Huang J, Montenegro G, Kushman A, Citrigno L, Price J, Speziani F, Pericak-Vance MA, Züchner S.
    Clin Genet; 2011 Jun; 79(6):523-30. PubMed ID: 20718791
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  • 12. Investigation of mitochondrial function in hereditary spastic paraparesis.
    McDermott CJ, Taylor RW, Hayes C, Johnson M, Bushby KM, Turnbull DM, Shaw PJ.
    Neuroreport; 2003 Mar 03; 14(3):485-8. PubMed ID: 12634509
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  • 13. An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion.
    Beetz C, Nygren AO, Deufel T, Reid E.
    Neurogenetics; 2007 Nov 03; 8(4):317-8. PubMed ID: 17657515
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  • 14. Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias.
    Reid E.
    J Med Genet; 2003 Feb 03; 40(2):81-6. PubMed ID: 12566514
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  • 20. SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.
    Patel H, Cross H, Proukakis C, Hershberger R, Bork P, Ciccarelli FD, Patton MA, McKusick VA, Crosby AH.
    Nat Genet; 2002 Aug 03; 31(4):347-8. PubMed ID: 12134148
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