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Journal Abstract Search

131 related items for PubMed ID: 15210518

  • 1. Hereditary spastic paraplegia: spastin phenotype and function.
    Fink JK, Rainier S.
    Arch Neurol; 2004 Jun; 61(6):830-3. PubMed ID: 15210518
    [No Abstract] [Full Text] [Related]

  • 2. Novel mutation of the Spastin gene in familial spastic paraplegia.
    De Bantel A, McWilliams S, Auysh D, Echol C, Sambuughin N, Sivakumar K.
    Clin Genet; 2001 May; 59(5):364-5. PubMed ID: 11359470
    [No Abstract] [Full Text] [Related]

  • 3. [Recent progress in genetic study of hereditary spastic paraplegia].
    Takano H, Kasuga K, Kobayashi H, Nishizawa M.
    No To Shinkei; 2003 Sep; 55(9):757-63. PubMed ID: 14571837
    [No Abstract] [Full Text] [Related]

  • 4. Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus.
    Charvin D, Cifuentes-Diaz C, Fonknechten N, Joshi V, Hazan J, Melki J, Betuing S.
    Hum Mol Genet; 2003 Jan 01; 12(1):71-8. PubMed ID: 12490534
    [Abstract] [Full Text] [Related]

  • 5. Molecular basis of inherited spastic paraplegias.
    Casari G, Rugarli E.
    Curr Opin Genet Dev; 2001 Jun 01; 11(3):336-42. PubMed ID: 11377972
    [Abstract] [Full Text] [Related]

  • 6. Neuropathology: many paths lead to hereditary spastic paraplegia.
    Gould RM, Brady ST.
    Curr Biol; 2004 Oct 26; 14(20):R903-4. PubMed ID: 15498485
    [Abstract] [Full Text] [Related]

  • 7. Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.
    Mc Monagle P, Byrne P, Burke T, Parfrey N, Hutchinson M.
    Neurology; 2001 Jan 09; 56(1):139. PubMed ID: 11148263
    [No Abstract] [Full Text] [Related]

  • 8. The spastin jigsaw puzzle: another missing piece found.
    Hedera P.
    Neurology; 2006 Dec 12; 67(11):1912-3. PubMed ID: 17159093
    [No Abstract] [Full Text] [Related]

  • 9. Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia.
    Tang B, Zhao G, Xia K, Pan Q, Luo W, Shen L, Long Z, Dai H, Zi X, Jiang H.
    Arch Neurol; 2004 Jan 12; 61(1):49-55. PubMed ID: 14732620
    [Abstract] [Full Text] [Related]

  • 10. Hereditary spastic paraplegia: the pace quickens.
    Fink JK.
    Ann Neurol; 2002 Jun 12; 51(6):669-72. PubMed ID: 12112070
    [No Abstract] [Full Text] [Related]

  • 11. First mutation in the nuclear localization signal sequence of spastin protein identified in a patient with hereditary spastic paraplegia.
    Magariello A, Tortorella C, Patitucci A, Tortelli R, Liguori M, Mazzei R, Conforti FL, Citrigno L, Ungaro C, Simone IL, Muglia M.
    Eur J Neurol; 2013 Jan 12; 20(1):e22-3. PubMed ID: 23279441
    [No Abstract] [Full Text] [Related]

  • 12. Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class.
    Yip AG, Dürr A, Marchuk DA, Ashley-Koch A, Hentati A, Rubinsztein DC, Reid E.
    J Med Genet; 2003 Sep 12; 40(9):e106. PubMed ID: 12960222
    [No Abstract] [Full Text] [Related]

  • 13. [Construction of wild-type and mutant SPAST vectors for the study of molecular mechanism of hereditary spastic paraplegia].
    Yan YP, Pu JL, Zhang BR, Zhao GH.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb 12; 30(1):9-12. PubMed ID: 23450470
    [Abstract] [Full Text] [Related]

  • 14. The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.
    Reid E, Connell J, Edwards TL, Duley S, Brown SE, Sanderson CM.
    Hum Mol Genet; 2005 Jan 01; 14(1):19-38. PubMed ID: 15537668
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 31(4):347-8. PubMed ID: 12134148
    [Abstract] [Full Text] [Related]

  • 16. Hereditary spastic paraparesis: disrupted intracellular transport associated with spastin mutation.
    McDermott CJ, Grierson AJ, Wood JD, Bingley M, Wharton SB, Bushby KM, Shaw PJ.
    Ann Neurol; 2003 Dec 01; 54(6):748-59. PubMed ID: 14681884
    [Abstract] [Full Text] [Related]

  • 17. Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia.
    Chelban V, Lynch DS, Houlden H, Wood N.
    J Neurol; 2016 Jun 01; 263(6):1232-3. PubMed ID: 27025852
    [No Abstract] [Full Text] [Related]

  • 18. Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics.
    Errico A, Ballabio A, Rugarli EI.
    Hum Mol Genet; 2002 Jan 15; 11(2):153-63. PubMed ID: 11809724
    [Abstract] [Full Text] [Related]

  • 19. Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.
    Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, Ben Hamida M, Hentati F, Siddique T.
    Neurology; 2000 Nov 14; 55(9):1388-90. PubMed ID: 11087788
    [Abstract] [Full Text] [Related]

  • 20. Infantile-onset ascending spastic paraplegia phenotype associated with SPAST mutation.
    de Souza PV, Bortholin T, Naylor FG, de Rezende Pinto WB, Oliveira AS.
    J Neurol Sci; 2016 Dec 15; 371():34-35. PubMed ID: 27871443
    [No Abstract] [Full Text] [Related]

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