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Journal Abstract Search

126 related items for PubMed ID: 3587641

  • 1. The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree.
    Boustany RM, Fleischnick E, Alper CA, Marazita ML, Spence MA, Martin JB, Kolodny EH.
    Neurology; 1987 Jun; 37(6):910-5. PubMed ID: 3587641
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  • 2. Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.
    Hazan J, Fontaine B, Bruyn RP, Lamy C, van Deutekom JC, Rime CS, Dürr A, Melki J, Lyon-Caen O, Agid Y.
    Hum Mol Genet; 1994 Sep; 3(9):1569-73. PubMed ID: 7833913
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  • 3. 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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  • 7. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.
    Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T.
    Hum Mol Genet; 1994 Aug; 3(8):1263-7. PubMed ID: 7987300
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  • 11. 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 Aug; 48(3):169-78. PubMed ID: 9618065
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  • 14. Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.
    Fontaine B, Rime CS, Hazan J, Dürr A, Stevanin G, Penet C, Reboul J, Agid Y, Lyon-Caen O, Baumann N.
    Neuromuscul Disord; 1995 Jan; 5(1):11-7. PubMed ID: 7719135
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  • 15. Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.
    Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A.
    Hum Genet; 1996 Sep; 98(3):371-5. PubMed ID: 8707310
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  • 16. A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity.
    Reid E, Dearlove AM, Rhodes M, Rubinsztein DC.
    Am J Hum Genet; 1999 Sep; 65(3):757-63. PubMed ID: 10441583
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  • 17. Recessively inherited 'pure' spastic paraplegia: case study.
    de Coo IF, Gabreëls FJ, Renier WO, Colon EJ, ter Haar BG.
    Clin Neurol Neurosurg; 1982 Sep; 84(4):247-53. PubMed ID: 6301736
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