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Journal Abstract Search

666 related items for PubMed ID: 21440262

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  • 2. 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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  • 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; 65(3):393-402. PubMed ID: 18332254
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  • 8. 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
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  • 9. A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.
    Boukhris A, Feki I, Elleuch N, Miladi MI, Boland-Augé A, Truchetto J, Mundwiller E, Jezequel N, Zelenika D, Mhiri C, Brice A, Stevanin G.
    Neurogenetics; 2010 Oct 15; 11(4):441-8. PubMed ID: 20593214
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  • 11. 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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  • 12. 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 25; 17(1):48-52. PubMed ID: 22246010
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  • 13. 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 25; 48(1):108-12. PubMed ID: 10894224
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  • 14. 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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  • 18. Expanding the clinical spectrum of SPG11 gene mutations in recessive hereditary spastic paraplegia with thin corpus callosum.
    Abdel Aleem A, Abu-Shahba N, Swistun D, Silhavy J, Bielas SL, Sattar S, Gleeson JG, Zaki MS.
    Eur J Med Genet; 2011 Jul 22; 54(1):82-5. PubMed ID: 20971220
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  • 20. Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration.
    Stevanin G, Azzedine H, Denora P, Boukhris A, Tazir M, Lossos A, Rosa AL, Lerer I, Hamri A, Alegria P, Loureiro J, Tada M, Hannequin D, Anheim M, Goizet C, Gonzalez-Martinez V, Le Ber I, Forlani S, Iwabuchi K, Meiner V, Uyanik G, Erichsen AK, Feki I, Pasquier F, Belarbi S, Cruz VT, Depienne C, Truchetto J, Garrigues G, Tallaksen C, Tranchant C, Nishizawa M, Vale J, Coutinho P, Santorelli FM, Mhiri C, Brice A, Durr A, SPATAX consortium.
    Brain; 2008 Mar 22; 131(Pt 3):772-84. PubMed ID: 18079167
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