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Journal Abstract Search

90 related items for PubMed ID: 16565863

  • 1. A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12.
    Züchner S, Kail ME, Nance MA, Gaskell PC, Svenson IK, Marchuk DA, Pericak-Vance MA, Ashley-Koch AE.
    Neurogenetics; 2006 May; 7(2):127-9. PubMed ID: 16565863
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  • 2. Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3.
    Huang S, Zhuyu, Li H, Labu, Baizhu, Lo WH, Fischer C, Vogel F.
    Hum Genet; 1997 Oct; 100(5-6):620-3. PubMed ID: 9341882
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  • 4. Familial spastic paraplegia: evidence for a fourth locus.
    Bruyn RP, van Veen MM, Kremer H, Scheltens PH, Padberg GW.
    Clin Neurol Neurosurg; 1997 May; 99(2):87-90. PubMed ID: 9213050
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  • 6. A large family with pure autosomal dominant hereditary spastic paraplegia from southern Italy mapping to chromosome 14q11.2-q24.3.
    Muglia M, Magariello A, Nicoletti G, Patitucci A, Gabriele AL, Conforti FL, Mazzei R, Caracciolo M, Casari G, Ardito B, Lastilla M, Gambardella A, Quattrone A.
    J Neurol; 2002 Oct; 249(10):1413-6. PubMed ID: 12382159
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  • 7. 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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  • 8. 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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  • 11. 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; 58(3):423-9. PubMed ID: 16130112
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  • 12. 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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  • 13. Novel locus for autosomal dominant pure hereditary spastic paraplegia (SPG19) maps to chromosome 9q33-q34.
    Valente EM, Brancati F, Caputo V, Bertini E, Patrono C, Costanti D, Dallapiccola B.
    Ann Neurol; 2002 Jun; 51(6):681-5. PubMed ID: 12112072
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  • 14. Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus).
    Munhoz RP, Kawarai T, Teive HA, Raskin S, Sato C, Liang Y, St George-Hyslop PH, Rogaeva E.
    Mov Disord; 2006 Feb; 21(2):279-81. PubMed ID: 16267846
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  • 15. Transcript map of the chromosome 2-linked autosomal dominant spastic paraplegia (SPG4) critical region and identification of a highly informative STRP.
    Lau EL, Kostrzewa M, Müller U.
    Neurogenetics; 1998 Dec; 2(1):75-6. PubMed ID: 9933304
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  • 17. Autosomal dominant hereditary spastic paraplegia with axonal sensory motor polyneuropathy maps to chromosome 21q 22.3.
    Peddareddygari LR, Hanna PA, Igo RP, Luo YA, Won S, Hirano M, Grewal RP.
    Int J Neurosci; 2016 Dec; 126(7):600-6. PubMed ID: 26000935
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