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Journal Abstract Search

166 related items for PubMed ID: 10751268

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

  • 2. Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance.
    Byrne PC, Webb S, McSweeney F, Burke T, Hutchinson M, Parfrey NA.
    Eur J Hum Genet; 1998 Apr 11; 6(3):275-82. PubMed ID: 9781032
    [Abstract] [Full Text] [Related]

  • 3. Autosomal dominant hereditary spastic paraparesis with cognitive loss linked to chromosome 2p.
    Webb S, Coleman D, Byrne P, Parfrey N, Burke T, Hutchinson J, Hutchinson M.
    Brain; 1998 Apr 11; 121 ( Pt 4)():601-9. PubMed ID: 9577388
    [Abstract] [Full Text] [Related]

  • 4. Further evidence of dementia in SPG4-linked autosomal dominant hereditary spastic paraplegia.
    McMonagle P, Byrne P, Hutchinson M.
    Neurology; 2004 Feb 10; 62(3):407-10. PubMed ID: 14872021
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Dementia in SPG4 hereditary spastic paraplegia: clinical, genetic, and neuropathologic evidence.
    Murphy S, Gorman G, Beetz C, Byrne P, Dytko M, McMonagle P, Kinsella K, Farrell M, Hutchinson M.
    Neurology; 2009 Aug 04; 73(5):378-84. PubMed ID: 19652142
    [Abstract] [Full Text] [Related]

  • 7. Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis.
    Webb S, Hutchinson M.
    Brain; 1998 May 04; 121 ( Pt 5)():923-9. PubMed ID: 9619194
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.
    Fontaine B, Davoine CS, Dürr A, Paternotte C, Feki I, Weissenbach J, Hazan J, Brice A.
    Am J Hum Genet; 2000 Feb 13; 66(2):702-7. PubMed ID: 10677329
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11. 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 13; 64(1):61-6. PubMed ID: 9436729
    [Abstract] [Full Text] [Related]

  • 12.
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  • 13. Large deletion involving the 5'-UTR in the spastin gene caused mild phenotype of autosomal dominant hereditary spastic paraplegia.
    Iwanaga H, Tsujino A, Shirabe S, Eguchi H, Fukushima N, Niikawa N, Yoshiura K, Eguchi K.
    Am J Med Genet A; 2005 Feb 15; 133A(1):13-7. PubMed ID: 15637712
    [Abstract] [Full Text] [Related]

  • 14. Clinical and pathologic findings in hereditary spastic paraparesis with spastin mutation.
    White KD, Ince PG, Lusher M, Lindsey J, Cookson M, Bashir R, Shaw PJ, Bushby KM.
    Neurology; 2000 Jul 12; 55(1):89-94. PubMed ID: 10891911
    [Abstract] [Full Text] [Related]

  • 15. Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
    Nielsen JE, Johnsen B, Koefoed P, Scheuer KH, Grønbech-Jensen M, Law I, Krabbe K, Nørremølle A, Eiberg H, Søndergård H, Dam M, Rehfeld JF, Krarup C, Paulson OB, Hasholt L, Sørensen SA.
    Eur J Neurol; 2004 Dec 12; 11(12):817-24. PubMed ID: 15667412
    [Abstract] [Full Text] [Related]

  • 16. 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 12; 64(2):563-9. PubMed ID: 9973294
    [Abstract] [Full Text] [Related]

  • 17. Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.
    Dürr A, Davoine CS, Paternotte C, von Fellenberg J, Cogilinicean S, Coutinho P, Lamy C, Bourgeois S, Prud'homme JF, Penet C, Mas JL, Burgunder JM, Hazan J, Weissenbach J, Brice A, Fontaine B.
    Brain; 1996 Oct 12; 119 ( Pt 5)():1487-96. PubMed ID: 8931574
    [Abstract] [Full Text] [Related]

  • 18. Phenotype of AD-HSP due to mutations in the SPAST gene: comparison with AD-HSP without mutations.
    McMonagle P, Byrne PC, Fitzgerald B, Webb S, Parfrey NA, Hutchinson M.
    Neurology; 2000 Dec 26; 55(12):1794-800. PubMed ID: 11134375
    [Abstract] [Full Text] [Related]

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  • 20. 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 26; 122(3-4):261-73. PubMed ID: 17605047
    [Abstract] [Full Text] [Related]

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