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Journal Abstract Search

337 related items for PubMed ID: 11354831

  • 1. Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
    Ashley-Koch A, Bonner ER, Gaskell PC, West SG, Tim R, Wolpert CM, Jones R, Farrell CD, Nance M, Svenson IK, Marchuk DA, Boustany RM, Vance JM, Scott WK, Pericak-Vance MA.
    Neurogenetics; 2001 Mar; 3(2):91-7. PubMed ID: 11354831
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  • 3. 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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  • 5. 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; 1(2):95-102. PubMed ID: 10732810
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  • 6. Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.
    Reid E, Dearlove AM, Whiteford ML, Rhodes M, Rubinsztein DC.
    Neurology; 1999 Nov 10; 53(8):1844-9. PubMed ID: 10563637
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  • 8. Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2.
    Raskind WH, Pericak-Vance MA, Lennon F, Wolff J, Lipe HP, Bird TD.
    Am J Med Genet; 1997 Feb 21; 74(1):26-36. PubMed ID: 9034002
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  • 12. 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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  • 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 03; 51(6):681-5. PubMed ID: 12112072
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  • 15. Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study.
    Nielsen JE, Krabbe K, Jennum P, Koefoed P, Jensen LN, Fenger K, Eiberg H, Hasholt L, Werdelin L, Sørensen SA.
    J Neurol Neurosurg Psychiatry; 1998 Jan 03; 64(1):61-6. PubMed ID: 9436729
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  • 17. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.
    Hazan J, Lamy C, Melki J, Munnich A, de Recondo J, Weissenbach J.
    Nat Genet; 1993 Oct 03; 5(2):163-7. PubMed ID: 8252041
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  • 18. Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.
    Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L.
    Neurology; 2009 Jun 02; 72(22):1893-8. PubMed ID: 19357379
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  • 20. 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 02; 137(2):131-8. PubMed ID: 8782167
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