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Journal Abstract Search

71 related items for PubMed ID: 9700778

  • 21.
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  • 22. A fine integrated map of the SPG4 locus excludes an expanded CAG repeat in chromosome 2p-linked autosomal dominant spastic paraplegia.
    Hazan J, Davoine CS, Mavel D, Fonknechten N, Paternotte C, Fizames C, Cruaud C, Samson D, Muselet D, Vega-Czarny N, Brice A, Gyapay G, Heilig R, Fontaine B, Weissenbach J.
    Genomics; 1999 Sep 15; 60(3):309-19. PubMed ID: 10493830
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  • 23.
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  • 24. Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3.
    Klebe S, Azzedine H, Durr A, Bastien P, Bouslam N, Elleuch N, Forlani S, Charon C, Koenig M, Melki J, Brice A, Stevanin G.
    Brain; 2006 Jun 15; 129(Pt 6):1456-62. PubMed ID: 16434418
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  • 26. [A case of autosomal dominant, pure form spastic paraplegia with thinning of the corpus callosum].
    Tomiyasu H, Hayashi R, Watanabe R, Honda M, Yoshii F.
    Rinsho Shinkeigaku; 1998 May 15; 38(5):435-9. PubMed ID: 9805990
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  • 29. Age-related cognitive decline in hereditary spastic paraparesis linked to chromosome 2p.
    Byrne PC, Mc Monagle P, Webb S, Fitzgerald B, Parfrey NA, Hutchinson M.
    Neurology; 2000 Apr 11; 54(7):1510-7. PubMed ID: 10751268
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  • 30.
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  • 31. A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease).
    Scheltens P, Bruyn RP, Hazenberg GJ.
    Acta Neurol Scand; 1990 Sep 11; 82(3):169-73. PubMed ID: 2270744
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  • 32.
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  • 33. Recent advances in hereditary spastic paraplegia.
    Tallaksen CM, Dürr A, Brice A.
    Curr Opin Neurol; 2001 Aug 11; 14(4):457-63. PubMed ID: 11470961
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  • 34. 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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  • 35. 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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  • 38. A clinical, genetic and candidate gene study of Silver syndrome, a complicated form of hereditary spastic paraplegia.
    Warner TT, Patel H, Proukakis C, Reed JA, McKie L, Wills A, Patton MA, Crosby AH.
    J Neurol; 2004 Sep 21; 251(9):1068-74. PubMed ID: 15372247
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  • 39.
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  • 40. [New variant of a rare neurocutaneous syndrome].
    Khannanova FK, Shamgunova SB, Ruzybakiev RM.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981 Sep 21; 81(3):338-42. PubMed ID: 7257675
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