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Journal Abstract Search

116 related items for PubMed ID: 8707310

  • 21. CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24.
    Nielsen JE, Koefoed P, Abell K, Hasholt L, Eiberg H, Fenger K, Niebuhr E, Sørensen SA.
    Hum Mol Genet; 1997 Oct; 6(11):1811-6. PubMed ID: 9302257
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  • 24. 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; 64(2):563-9. PubMed ID: 9973294
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  • 25. '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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  • 27. Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.
    Paternotte C, Rudnicki D, Fizames C, Davoine CS, Mavel D, Dürr A, Samson D, Marquette C, Muselet D, Vega-Czarny N, Drouot N, Voit T, Fontaine B, Gyapay G, Auburger G, Weissenbach J, Hazan J.
    Genome Res; 1998 Nov; 8(11):1216-27. PubMed ID: 9847083
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  • 28. Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophin.
    Rocco P, Vainzof M, Froehner SC, Peters MF, Marie SK, Passos-Bueno MR, Zatz M.
    Am J Med Genet; 2000 May 15; 92(2):122-7. PubMed ID: 10797436
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  • 30. 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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  • 31. A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3.
    De Michele G, De Fusco M, Cavalcanti F, Filla A, Marconi R, Volpe G, Monticelli A, Ballabio A, Casari G, Cocozza S.
    Am J Hum Genet; 1998 Jul 21; 63(1):135-9. PubMed ID: 9634528
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  • 32. 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 21; 5(1):11-7. PubMed ID: 7719135
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  • 33. 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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  • 35. 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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  • 36. Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus.
    Muglia M, Criscuolo C, Magariello A, De Michele G, Scarano V, D'Adamo P, Ambrosio G, Gabriele AL, Patitucci A, Mazzei R, Conforti FL, Sprovieri T, Morgante L, Epifanio A, La Spina P, Valentino P, Gasparini P, Filla A, Quattrone A.
    Neurogenetics; 2004 Feb 02; 5(1):49-54. PubMed ID: 14658060
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  • 37. 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 02; 37(6):910-5. PubMed ID: 3587641
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  • 38. 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 02; 51(6):681-5. PubMed ID: 12112072
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  • 39. Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family.
    Fink JK, Sharp GB, Lange BM, Wu CB, Haley T, Otterud B, Peacock M, Leppert M.
    Neurology; 1995 Feb 02; 45(2):325-31. PubMed ID: 7854534
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  • 40. 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 Feb 02; 48(3):169-78. PubMed ID: 9618065
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