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Journal Abstract Search

199 related items for PubMed ID: 11470961

  • 1. Recent advances in hereditary spastic paraplegia.
    Tallaksen CM, Dürr A, Brice A.
    Curr Opin Neurol; 2001 Aug; 14(4):457-63. PubMed ID: 11470961
    [Abstract] [Full Text] [Related]

  • 2. Current insights into familial spastic paraparesis: new advances in an old disease.
    Fortini D, Cricchi F, Di Fabio R, Damiano M, Comanducci G, Benedetti L, Valoppi M, Grieco GS, D'Eugenio O, Celato A, Santorelli F, Casali C, Amabile GA, Pierelli F.
    Funct Neurol; 2003 Aug; 18(1):43-9. PubMed ID: 12760414
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary spastic paraplegias].
    Finsterer J.
    Nervenarzt; 2003 Jun; 74(6):497-504. PubMed ID: 12799788
    [Abstract] [Full Text] [Related]

  • 4. Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group.
    Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T.
    Neurology; 1996 Jun; 46(6):1507-14. PubMed ID: 8649538
    [Abstract] [Full Text] [Related]

  • 5. 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; 137(2):131-8. PubMed ID: 8782167
    [Abstract] [Full Text] [Related]

  • 6. Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.
    Coutinho P, Barros J, Zemmouri R, Guimarães J, Alves C, Chorão R, Lourenço E, Ribeiro P, Loureiro JL, Santos JV, Hamri A, Paternotte C, Hazan J, Silva MC, Prud'homme JF, Grid D.
    Arch Neurol; 1999 Aug; 56(8):943-9. PubMed ID: 10448799
    [Abstract] [Full Text] [Related]

  • 7. Advances in the hereditary spastic paraplegias.
    Fink JK.
    Exp Neurol; 2003 Nov; 184 Suppl 1():S106-10. PubMed ID: 14597333
    [Abstract] [Full Text] [Related]

  • 8. [AAA ATPases and hereditary spastic paraplegia].
    Wang YG, Shen L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):298-301. PubMed ID: 19504443
    [Abstract] [Full Text] [Related]

  • 9. Clinical features and management of hereditary spastic paraplegia.
    Faber I, Servelhere KR, Martinez AR, D'Abreu A, Lopes-Cendes I, França MC.
    Arq Neuropsiquiatr; 2014 Mar; 72(3):219-26. PubMed ID: 24676440
    [Abstract] [Full Text] [Related]

  • 10. [Ataxias and hereditary spastic paraplegias].
    Schüle R, Schöls L.
    Nervenarzt; 2017 Jul; 88(7):720-727. PubMed ID: 28600743
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation.
    Fink JK, Hedera P.
    Semin Neurol; 1999 Jul 13; 19(3):301-9. PubMed ID: 12194386
    [Abstract] [Full Text] [Related]

  • 13. Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.
    Sauter S, Miterski B, Klimpe S, Bönsch D, Schöls L, Visbeck A, Papke T, Hopf HC, Engel W, Deufel T, Epplen JT, Neesen J.
    Hum Mutat; 2002 Aug 13; 20(2):127-32. PubMed ID: 12124993
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Clinical and genetic heterogeneity in hereditary spastic paraplegias: from SPG1 to SPG72 and still counting.
    Klebe S, Stevanin G, Depienne C.
    Rev Neurol (Paris); 2015 Jun 02; 171(6-7):505-30. PubMed ID: 26008818
    [Abstract] [Full Text] [Related]

  • 16. Hereditary spastic paraplegia.
    Fink JK.
    Neurol Clin; 2002 Aug 02; 20(3):711-26. PubMed ID: 12432827
    [Abstract] [Full Text] [Related]

  • 17. CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5.
    Goizet C, Boukhris A, Durr A, Beetz C, Truchetto J, Tesson C, Tsaousidou M, Forlani S, Guyant-Maréchal L, Fontaine B, Guimarães J, Isidor B, Chazouillères O, Wendum D, Grid D, Chevy F, Chinnery PF, Coutinho P, Azulay JP, Feki I, Mochel F, Wolf C, Mhiri C, Crosby A, Brice A, Stevanin G.
    Brain; 2009 Jun 02; 132(Pt 6):1589-600. PubMed ID: 19439420
    [Abstract] [Full Text] [Related]

  • 18. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A.
    Abel A, Fonknechten N, Hofer A, Dürr A, Cruaud C, Voit T, Weissenbach J, Brice A, Klimpe S, Auburger G, Hazan J.
    Neurogenetics; 2004 Dec 02; 5(4):239-43. PubMed ID: 15517445
    [Abstract] [Full Text] [Related]

  • 19. [From gene to disease; spastin and hereditary spastic paraparesis].
    Bruyn RP, Frants RR.
    Ned Tijdschr Geneeskd; 2004 Jan 24; 148(4):179-81. PubMed ID: 14974310
    [Abstract] [Full Text] [Related]

  • 20. Hereditary spastic paraplegias: an update.
    Depienne C, Stevanin G, Brice A, Durr A.
    Curr Opin Neurol; 2007 Dec 24; 20(6):674-80. PubMed ID: 17992088
    [Abstract] [Full Text] [Related]

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