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Journal Abstract Search

196 related items for PubMed ID: 14681889

  • 1. A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32.
    Blumen SC, Bevan S, Abu-Mouch S, Negus D, Kahana M, Inzelberg R, Mazarib A, Mahamid A, Carasso RL, Slor H, Withers D, Nisipeanu P, Navon R, Reid E.
    Ann Neurol; 2003 Dec; 54(6):796-803. PubMed ID: 14681889
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  • 2. A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.
    Meijer IA, Cossette P, Roussel J, Benard M, Toupin S, Rouleau GA.
    Ann Neurol; 2004 Oct; 56(4):579-82. PubMed ID: 15455396
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  • 3. 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; 48(1):108-12. PubMed ID: 10894224
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  • 4. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
    Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L.
    Neurology; 2009 Jun 02; 72(22):1893-8. PubMed ID: 19357379
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  • 5. 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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  • 6. Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28).
    Bouslam N, Benomar A, Azzedine H, Bouhouche A, Namekawa M, Klebe S, Charon C, Durr A, Ruberg M, Brice A, Yahyaoui M, Stevanin G.
    Ann Neurol; 2005 Apr 15; 57(4):567-71. PubMed ID: 15786464
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  • 9. A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.
    Dick KJ, Al-Mjeni R, Baskir W, Koul R, Simpson MA, Patton MA, Raeburn S, Crosby AH.
    Neurology; 2008 Jul 22; 71(4):248-52. PubMed ID: 18463364
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  • 12. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.
    Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J.
    Nat Genet; 1993 Oct 22; 5(2):163-7. PubMed ID: 8252041
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  • 13. A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14.
    Wilkinson PA, Simpson MA, Bastaki L, Patel H, Reed JA, Kalidas K, Samilchuk E, Khan R, Warner TT, Crosby AH.
    J Med Genet; 2005 Jan 22; 42(1):80-2. PubMed ID: 15635080
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  • 16. New locus for hereditary spastic paraplegia maps to chromosome 1p31.1-1p21.1.
    Orlacchio A, Kawarai T, Gaudiello F, St George-Hyslop PH, Floris R, Bernardi G.
    Ann Neurol; 2005 Sep 22; 58(3):423-9. PubMed ID: 16130112
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