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Journal Abstract Search

190 related items for PubMed ID: 10408536

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 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 13; 137(2):131-8. PubMed ID: 8782167
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  • 3. Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
    Fink JK, Wu CT, Jones SM, Sharp GB, Lange BM, Lesicki A, Reinglass T, Varvil T, Otterud B, Leppert M.
    Am J Hum Genet; 1995 Jan 13; 56(1):188-92. PubMed ID: 7825577
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  • 4. Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.
    Hazan J, Fontaine B, Bruyn RP, Lamy C, van Deutekom JC, Rime CS, Dürr A, Melki J, Lyon-Caen O, Agid Y.
    Hum Mol Genet; 1994 Sep 13; 3(9):1569-73. PubMed ID: 7833913
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  • 5. Phenotypic analysis of autosomal dominant hereditary spastic paraplegia linked to chromosome 8q.
    Hedera P, DiMauro S, Bonilla E, Wald J, Eldevik OP, Fink JK.
    Neurology; 1999 Jul 13; 53(1):44-50. PubMed ID: 10408535
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  • 6. A new locus for autosomal recessive spastic paraplegia associated with mental retardation and distal motor neuropathy, SPG14, maps to chromosome 3q27-q28.
    Vazza G, Zortea M, Boaretto F, Micaglio GF, Sartori V, Mostacciuolo ML.
    Am J Hum Genet; 2000 Aug 13; 67(2):504-9. PubMed ID: 10877981
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  • 7. 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 13; 35(2):89-93. PubMed ID: 9507385
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  • 8. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.
    Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T.
    Hum Mol Genet; 1994 Aug 13; 3(8):1263-7. PubMed ID: 7987300
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  • 9. Linkage of autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum to chromosome 15A13-15.
    Shibasaki Y, Tanaka H, Iwabuchi K, Kawasaki S, Kondo H, Uekawa K, Ueda M, Kamiya T, Katayama Y, Nakamura A, Takashima H, Nakagawa M, Masuda M, Utsumi H, Nakamuro T, Tada K, Kurohara K, Inoue K, Koike F, Sakai T, Tsuji S, Kobayashi H.
    Ann Neurol; 2000 Jul 13; 48(1):108-12. PubMed ID: 10894224
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  • 10. 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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  • 14. Familial spastic paraplegia: evidence for a fourth locus.
    Bruyn RP, van Veen MM, Kremer H, Scheltens PH, Padberg GW.
    Clin Neurol Neurosurg; 1997 May 13; 99(2):87-90. PubMed ID: 9213050
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  • 18. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum.
    Casali C, Valente EM, Bertini E, Montagna G, Criscuolo C, De Michele G, Villanova M, Damiano M, Pierallini A, Brancati F, Scarano V, Tessa A, Cricchi F, Grieco GS, Muglia M, Carella M, Martini B, Rossi A, Amabile GA, Nappi G, Filla A, Dallapiccola B, Santorelli FM.
    Neurology; 2004 Jan 27; 62(2):262-8. PubMed ID: 14745065
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  • 19. Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3.
    Huang S, Zhuyu, Li H, Labu, Baizhu, Lo WH, Fischer C, Vogel F.
    Hum Genet; 1997 Oct 27; 100(5-6):620-3. PubMed ID: 9341882
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