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Journal Abstract Search

135 related items for PubMed ID: 17503452

  • 1.
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  • 2. Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families.
    Elleuch N, Bouslam N, Hanein S, Lossos A, Hamri A, Klebe S, Meiner V, Birouk N, Lerer I, Grid D, Bacq D, Tazir M, Zelenika D, Argov Z, Durr A, Yahyaoui M, Benomar A, Brice A, Stevanin G.
    Neurogenetics; 2007 Nov; 8(4):307-15. PubMed ID: 17661097
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  • 4. Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
    Muglia M, Criscuolo C, Magariello A, De Michele G, Scarano V, D'Adamo P, Ambrosio G, Gabriele AL, Patitucci A, Mazzei R, Conforti FL, Sprovieri T, Morgante L, Epifanio A, La Spina P, Valentino P, Gasparini P, Filla A, Quattrone A.
    Neurogenetics; 2004 Feb; 5(1):49-54. PubMed ID: 14658060
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  • 7. 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; 57(4):567-71. PubMed ID: 15786464
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  • 8. 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; 11(4):441-8. PubMed ID: 20593214
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  • 12. Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.
    Stevanin G, Montagna G, Azzedine H, Valente EM, Durr A, Scarano V, Bouslam N, Cassandrini D, Denora PS, Criscuolo C, Belarbi S, Orlacchio A, Jonveaux P, Silvestri G, Hernandez AM, De Michele G, Tazir M, Mariotti C, Brockmann K, Malandrini A, van der Knapp MS, Neri M, Tonekaboni H, Melone MA, Tessa A, Dotti MT, Tosetti M, Pauri F, Federico A, Casali C, Cruz VT, Loureiro JL, Zara F, Forlani S, Bertini E, Coutinho P, Filla A, Brice A, Santorelli FM.
    Neurogenetics; 2006 Jul; 7(3):149-56. PubMed ID: 16699786
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  • 13. A new phenotype linked to SPG27 and refinement of the critical region on chromosome.
    Ribai P, Stevanin G, Bouslam N, Pontier B, Nelson I, Fontaine B, Dussert C, Charon C, Durr A, Brice A.
    J Neurol; 2006 Jun; 253(6):714-9. PubMed ID: 16511635
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  • 16. A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
    Hanein S, Dürr A, Ribai P, Forlani S, Leutenegger AL, Nelson I, Babron MC, Elleuch N, Depienne C, Charon C, Brice A, Stevanin G.
    Hum Genet; 2007 Nov; 122(3-4):261-73. PubMed ID: 17605047
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  • 18. Clinical and genetic analysis of Taiwanese patients with hereditary spastic paraplegia type 5.
    Lan MY, Yeh TH, Chang YY, Kuo HC, Sun HS, Lai SC, Lu CS.
    Eur J Neurol; 2015 Jan; 22(1):211-4. PubMed ID: 24641183
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