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Pubmed for Handhelds

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Journal Abstract Search

146 related items for PubMed ID: 9109738

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  • 8. 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; 7(11):1779-86. PubMed ID: 9736780
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  • 10. Spastic paraplegia, ataxia, mental retardation (SPAR): a novel genetic disorder.
    Hedera P, Rainier S, Zhao XP, Schalling M, Lindblad K, Yuan QP, Ikeuchi T, Trobe J, Wald JJ, Eldevik OP, Kluin K, Fink JK.
    Neurology; 2002 Feb 12; 58(3):411-6. PubMed ID: 11839840
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  • 12. Familial spastic paraplegia: evidence for a fourth locus.
    Bruyn RP, van Veen MM, Kremer H, Scheltens PH, Padberg GW.
    Clin Neurol Neurosurg; 1997 May 12; 99(2):87-90. PubMed ID: 9213050
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  • 13. 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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  • 15. Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family.
    Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A.
    Hum Genet; 1996 Sep 13; 98(3):371-5. PubMed ID: 8707310
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