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Journal Abstract Search

341 related items for PubMed ID: 17516453

  • 1. Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum.
    França MC, D'Abreu A, Maurer-Morelli CV, Seccolin R, Appenzeller S, Alessio A, Damasceno BP, Nucci A, Cendes F, Lopes-Cendes I.
    Mov Disord; 2007 Aug 15; 22(11):1556-62. PubMed ID: 17516453
    [Abstract] [Full Text] [Related]

  • 2. Hereditary spastic paraplegia with thin corpus callosum: reduction of the SPG11 interval and evidence for further genetic heterogeneity.
    Lossos A, Stevanin G, Meiner V, Argov Z, Bouslam N, Newman JP, Gomori JM, Klebe S, Lerer I, Elleuch N, Silverstein S, Durr A, Abramsky O, Ben-Nariah Z, Brice A.
    Arch Neurol; 2006 May 15; 63(5):756-60. PubMed ID: 16682547
    [Abstract] [Full Text] [Related]

  • 3. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11).
    Winner B, Uyanik G, Gross C, Lange M, Schulte-Mattler W, Schuierer G, Marienhagen J, Hehr U, Winkler J.
    Arch Neurol; 2004 Jan 15; 61(1):117-21. PubMed ID: 14732628
    [Abstract] [Full Text] [Related]

  • 4. Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
    Boukhris A, Stevanin G, Feki I, Denis E, Elleuch N, Miladi MI, Truchetto J, Denora P, Belal S, Mhiri C, Brice A.
    Arch Neurol; 2008 Mar 15; 65(3):393-402. PubMed ID: 18332254
    [Abstract] [Full Text] [Related]

  • 5. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum.
    Olmez A, Uyanik G, Ozgül RK, Gross C, Cirak S, Elibol B, Anlar B, Winner B, Hehr U, Topaloglu H, Winkler J.
    Neuropediatrics; 2006 Apr 15; 37(2):59-66. PubMed ID: 16773502
    [Abstract] [Full Text] [Related]

  • 6. Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.
    Brockmann K, Simpson MA, Faber A, Bönnemann C, Crosby AH, Gärtner J.
    Neuropediatrics; 2005 Aug 15; 36(4):274-8. PubMed ID: 16138254
    [Abstract] [Full Text] [Related]

  • 7. Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases.
    Tang BS, Chen X, Zhao GH, Shen L, Yan XX, Jiang H, Luo W.
    Chin Med J (Engl); 2004 Jul 15; 117(7):1002-5. PubMed ID: 15265372
    [Abstract] [Full Text] [Related]

  • 8. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.
    Shibasaki Y, Tanaka H, Iwabuchi K, Kawasaki S, Kondo H, Uekawa K, Ueda M, Kamiya T, Katayama Y, Nakamura A, Takashima H, Nakagawa M, Masuda M, Utsumi H, Nakamuro T, Tada K, Kurohara K, Inoue K, Koike F, Sakai T, Tsuji S, Kobayashi H.
    Ann Neurol; 2000 Jul 15; 48(1):108-12. PubMed ID: 10894224
    [Abstract] [Full Text] [Related]

  • 9. A new locus (SPG47) maps to 1p13.2-1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum.
    Blumkin L, Lerman-Sagie T, Lev D, Yosovich K, Leshinsky-Silver E.
    J Neurol Sci; 2011 Jun 15; 305(1-2):67-70. PubMed ID: 21440262
    [Abstract] [Full Text] [Related]

  • 10. Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.
    Gucuyener K, Hirfanoglu T, Ok I, Cansu A, Serdaroglu A.
    J Child Neurol; 2007 Feb 15; 22(2):214-7. PubMed ID: 17621486
    [Abstract] [Full Text] [Related]

  • 11. Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum.
    Chen Q, Lui S, Wang JG, Ou-Yang L, Zhou D, Burgunder JM, Gong QY, Shang HF.
    Neurosci Lett; 2008 Aug 15; 441(1):21-4. PubMed ID: 18586399
    [Abstract] [Full Text] [Related]

  • 12. Forceps minor region signal abnormality "ears of the lynx": an early MRI finding in spastic paraparesis with thin corpus callosum and mutations in the spatacsin gene (SPG11) on chromosome 15.
    Riverol M, Samaranch L, Pascual B, Pastor P, Irigoyen J, Pastor MA, de Castro P, Masdeu JC.
    J Neuroimaging; 2009 Jan 15; 19(1):52-60. PubMed ID: 19040626
    [Abstract] [Full Text] [Related]

  • 13. [A case of autosomal dominant, pure form spastic paraplegia with thinning of the corpus callosum].
    Tomiyasu H, Hayashi R, Watanabe R, Honda M, Yoshii F.
    Rinsho Shinkeigaku; 1998 May 15; 38(5):435-9. PubMed ID: 9805990
    [Abstract] [Full Text] [Related]

  • 14. Autosomal recessive hereditary spastic paraparesis with thin corpus callosum; report of two sisters.
    Vucic S, Lye T, Dunn G, Corbett A.
    J Clin Neurosci; 2004 May 15; 11(4):427-30. PubMed ID: 15080965
    [Abstract] [Full Text] [Related]

  • 15. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34.
    Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B.
    Brain; 2006 Sep 15; 129(Pt 9):2332-40. PubMed ID: 16672289
    [Abstract] [Full Text] [Related]

  • 16. [Three patients of complicated form of autosomal recessive hereditary spastic paraplegia associated with hypoplasia of the corpus callosum].
    Iwabuchi K, Kubota Y, Hanihara T, Nagatomo H.
    No To Shinkei; 1994 Oct 15; 46(10):941-7. PubMed ID: 7826709
    [Abstract] [Full Text] [Related]

  • 17. Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis.
    Wakil SM, Murad HN, Baz BM, Hagos ST, Al-Amr RA, Al-Yamani SA, Al-Wadaee SM, Meyer BF, Bohlega SA.
    Neurosciences (Riyadh); 2012 Jan 15; 17(1):48-52. PubMed ID: 22246010
    [Abstract] [Full Text] [Related]

  • 18. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.
    Casali C, Valente EM, Bertini E, Montagna G, Criscuolo C, De Michele G, Villanova M, Damiano M, Pierallini A, Brancati F, Scarano V, Tessa A, Cricchi F, Grieco GS, Muglia M, Carella M, Martini B, Rossi A, Amabile GA, Nappi G, Filla A, Dallapiccola B, Santorelli FM.
    Neurology; 2004 Jan 27; 62(2):262-8. PubMed ID: 14745065
    [Abstract] [Full Text] [Related]

  • 19. A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy.
    Al-Yahyaee S, Al-Gazali LI, De Jonghe P, Al-Barwany H, Al-Kindi M, De Vriendt E, Chand P, Koul R, Jacob PC, Gururaj A, Sztriha L, Parrado A, Van Broeckhoven C, Bayoumi RA.
    Neurology; 2006 Apr 25; 66(8):1230-4. PubMed ID: 16636240
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