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Journal Abstract Search

142 related items for PubMed ID: 2270744

  • 1. A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease).
    Scheltens P, Bruyn RP, Hazenberg GJ.
    Acta Neurol Scand; 1990 Sep; 82(3):169-73. PubMed ID: 2270744
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  • 2. Extensive genetic heterogeneity in the "pure" form of autosomal dominant familial spastic paraplegia (Strümpell's disease).
    Kobayashi H, Garcia CA, Tay PN, Hoffman EP.
    Muscle Nerve; 1996 Nov; 19(11):1435-8. PubMed ID: 8874401
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  • 3. Strumpell's pure familial spastic paraplegia: case study and review of the literature.
    Holmes GL, Shaywitz BA.
    J Neurol Neurosurg Psychiatry; 1977 Oct; 40(10):1003-8. PubMed ID: 591968
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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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  • 5. Hereditary "pure" spastic paraplegia: a study of nine families.
    Polo JM, Calleja J, Combarros O, Berciano J.
    J Neurol Neurosurg Psychiatry; 1993 Feb; 56(2):175-81. PubMed ID: 8382269
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  • 6. The neuropathology of hereditary spastic paraparesis.
    Bruyn RP.
    Clin Neurol Neurosurg; 1992 Feb; 94 Suppl():S16-8. PubMed ID: 1320499
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  • 8. 'Complicated' autosomal dominant familial spastic paraplegia is genetically distinct from 'pure' forms.
    Meierkord H, Nürnberg P, Mainz A, Marczinek K, Mrug M, Hampe J.
    Arch Neurol; 1997 Apr; 54(4):379-84. PubMed ID: 9109738
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  • 9. 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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  • 17. Hereditary spastic paraparesis. Clinical and genetic data from a large Dutch family.
    Bruyn RP, van Deutekom J, Frants RR, Padberg GW.
    Clin Neurol Neurosurg; 1993 Jun; 95(2):125-9. PubMed ID: 8344010
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  • 18. Clinical heterogeneity of familial spastic paraplegia linked to chromosome 2p21.
    Nance MA, Raabe WA, Midani H, Kolodny EH, David WS, Megna L, Pericak-Vance MA, Haines JL.
    Hum Hered; 1998 Jun; 48(3):169-78. PubMed ID: 9618065
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