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Journal Abstract Search

673 related items for PubMed ID: 16672289

  • 1. 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; 129(Pt 9):2332-40. PubMed ID: 16672289
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  • 2. Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.
    Klebe S, Azzedine H, Durr A, Bastien P, Bouslam N, Elleuch N, Forlani S, Charon C, Koenig M, Melki J, Brice A, Stevanin G.
    Brain; 2006 Jun; 129(Pt 6):1456-62. PubMed ID: 16434418
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  • 7. 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; 36(4):274-8. PubMed ID: 16138254
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  • 8. 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; 61(1):117-21. PubMed ID: 14732628
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  • 9. [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; 38(5):435-9. PubMed ID: 9805990
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  • 11. 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; 37(2):59-66. PubMed ID: 16773502
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  • 14. 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
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  • 17. A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.
    Gilbert DL, Leslie EJ, Keddache M, Leslie ND.
    Mov Disord; 2009 Feb 15; 24(3):364-70. PubMed ID: 19006192
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  • 18. 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
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  • 20. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p.
    Stevanin G, Bouslam N, Thobois S, Azzedine H, Ravaux L, Boland A, Schalling M, Broussolle E, Dürr A, Brice A.
    Ann Neurol; 2004 Jan 15; 55(1):97-104. PubMed ID: 14705117
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