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Journal Abstract Search

133 related items for PubMed ID: 8874401

  • 1. 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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  • 2. Molecular genetics of familial spastic paraplegia: a multitude of responsible genes.
    Kobayashi H, Garcia CA, Alfonso G, Marks HG, Hoffman EP.
    J Neurol Sci; 1996 May; 137(2):131-8. PubMed ID: 8782167
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  • 7. '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. Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.
    Heinzlef O, Paternotte C, Mahieux F, Prud'homme JF, Dien J, Madigand M, Pouget J, Weissenbach J, Roullet E, Hazan J.
    J Med Genet; 1998 Feb; 35(2):89-93. PubMed ID: 9507385
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  • 13. Autosomal dominant spastic paraplegia linked to chromosome 2p: clinical and genetic studies of a large Japanese pedigree.
    Matsuura T, Sasaki H, Wakisaka A, Hamada T, Moriwaka F, Tashiro K.
    J Neurol Sci; 1997 Oct 03; 151(1):65-70. PubMed ID: 9335012
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  • 15. Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q.
    Hedera P, Rainier S, Alvarado D, Zhao X, Williamson J, Otterud B, Leppert M, Fink JK.
    Am J Hum Genet; 1999 Feb 03; 64(2):563-9. PubMed ID: 9973294
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  • 16. Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13-15.
    Martínez Murillo F, Kobayashi H, Pegoraro E, Galluzzi G, Creel G, Mariani C, Farina E, Ricci E, Alfonso G, Pauli RM, Hoffman EP.
    Neurology; 1999 Jul 13; 53(1):50-6. PubMed ID: 10408536
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  • 17. 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 Jul 13; 48(3):169-78. PubMed ID: 9618065
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  • 18. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
    Scott WK, Gaskell PC, Lennon F, Wolpert CM, Menold MM, Aylsworth AS, Warner C, Farrell CD, Boustany RM, Albright SG, Boyd E, Kingston HM, Cumming WJ, Vance JM, Pericak-Vance MA.
    Neurogenetics; 1997 Sep 13; 1(2):95-102. PubMed ID: 10732810
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  • 19. A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease).
    Scheltens P, Bruyn RP, Hazenberg GJ.
    Acta Neurol Scand; 1990 Sep 13; 82(3):169-73. PubMed ID: 2270744
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  • 20. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
    Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S.
    Hum Mol Genet; 1994 Oct 13; 3(10):1867-71. PubMed ID: 7849714
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