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Journal Abstract Search

190 related items for PubMed ID: 10408536

  • 21. A novel locus for autosomal dominant "uncomplicated" hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3.
    Hanein S, Dürr A, Ribai P, Forlani S, Leutenegger AL, Nelson I, Babron MC, Elleuch N, Depienne C, Charon C, Brice A, Stevanin G.
    Hum Genet; 2007 Nov; 122(3-4):261-73. PubMed ID: 17605047
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  • 22. 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; 64(1):61-6. PubMed ID: 9436729
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  • 23. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11).
    Winner B, Uyanik G, Gross C, Lange M, Schulte-Mattler W, Schuierer G, Marienhagen J, Hehr U, Winkler J.
    Arch Neurol; 2004 Jan; 61(1):117-21. PubMed ID: 14732628
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  • 26. 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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  • 28. 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 10; 65(3):757-63. PubMed ID: 10441583
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  • 31. Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity.
    Gispert S, Santos N, Damen R, Voit T, Schulz J, Klockgether T, Orozco G, Kreuz F, Weissenbach J, Auburger G.
    Am J Hum Genet; 1995 Jan 10; 56(1):183-7. PubMed ID: 7825576
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  • 32. 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 10; 129(Pt 6):1456-62. PubMed ID: 16434418
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  • 33. Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia. A clinical and molecular genetic study of 28 United Kingdom families.
    Reid E, Grayson C, Rogers MT, Rubinsztein DC.
    Brain; 1999 Sep 10; 122 ( Pt 9)():1741-55. PubMed ID: 10468513
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  • 34. 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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  • 35. Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity.
    Stevanin G, Montagna G, Azzedine H, Valente EM, Durr A, Scarano V, Bouslam N, Cassandrini D, Denora PS, Criscuolo C, Belarbi S, Orlacchio A, Jonveaux P, Silvestri G, Hernandez AM, De Michele G, Tazir M, Mariotti C, Brockmann K, Malandrini A, van der Knapp MS, Neri M, Tonekaboni H, Melone MA, Tessa A, Dotti MT, Tosetti M, Pauri F, Federico A, Casali C, Cruz VT, Loureiro JL, Zara F, Forlani S, Bertini E, Coutinho P, Filla A, Brice A, Santorelli FM.
    Neurogenetics; 2006 Jul 11; 7(3):149-56. PubMed ID: 16699786
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  • 36. [Gene screening in five Chinese families with hereditary spastic paraplegia with thin corpus callosum].
    Zhao GH, Guo P, Ren ZJ, Liu XM, Shen L, Xia K, Tang BS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec 11; 24(6):677-80. PubMed ID: 18067082
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  • 37. CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients.
    Benson KF, Horwitz M, Wolff J, Friend K, Thompson E, White S, Richards RI, Raskind WH, Bird TD.
    Hum Mol Genet; 1998 Oct 11; 7(11):1779-86. PubMed ID: 9736780
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  • 38. A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.
    Meijer IA, Cossette P, Roussel J, Benard M, Toupin S, Rouleau GA.
    Ann Neurol; 2004 Oct 11; 56(4):579-82. PubMed ID: 15455396
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  • 39. 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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  • 40. Further evidence for a fourth gene causing X-linked pure spastic paraplegia.
    Starling A, Rocco P, Cambi F, Hobson GM, Passos Bueno MR, Zatz M.
    Am J Med Genet; 2002 Aug 01; 111(2):152-6. PubMed ID: 12210342
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