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Journal Abstract Search

255 related items for PubMed ID: 16143870

  • 1.
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  • 2. Magnetic resonance investigation of the upper spinal cord in pure and complicated hereditary spastic paraparesis.
    Sperfeld AD, Baumgartner A, Kassubek J.
    Eur Neurol; 2005; 54(4):181-5. PubMed ID: 16352904
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  • 4. 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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  • 5. Spinal Cord Gray and White Matter Damage in Different Hereditary Spastic Paraplegia Subtypes.
    Servelhere KR, Casseb RF, de Lima FD, Rezende TJR, Ramalho LP, França MC.
    AJNR Am J Neuroradiol; 2021 Mar 13; 42(3):610-615. PubMed ID: 33478946
    [Abstract] [Full Text] [Related]

  • 6. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.
    Fink JK.
    Acta Neuropathol; 2013 Sep 13; 126(3):307-28. PubMed ID: 23897027
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  • 7. Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.
    Crippa F, Panzeri C, Martinuzzi A, Arnoldi A, Redaelli F, Tonelli A, Baschirotto C, Vazza G, Mostacciuolo ML, Daga A, Orso G, Profice P, Trabacca A, D'Angelo MG, Comi GP, Galbiati S, Lamperti C, Bonato S, Pandolfo M, Meola G, Musumeci O, Toscano A, Trevisan CP, Bresolin N, Bassi MT.
    Arch Neurol; 2006 May 13; 63(5):750-5. PubMed ID: 16682546
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  • 8. Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage.
    Agosta F, Scarlato M, Spinelli EG, Canu E, Benedetti S, Bassi MT, Casali C, Sessa M, Copetti M, Pagani E, Comi G, Ferrari M, Falini A, Filippi M.
    Radiology; 2015 Jul 13; 276(1):207-18. PubMed ID: 25611737
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  • 9. 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 13; 5(4):239-43. PubMed ID: 15517445
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  • 10. TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation.
    Martinez-Lage M, Molina-Porcel L, Falcone D, McCluskey L, Lee VM, Van Deerlin VM, Trojanowski JQ.
    Acta Neuropathol; 2012 Aug 13; 124(2):285-91. PubMed ID: 22302102
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  • 11. MR imaging findings in autosomal recessive hereditary spastic paraplegia.
    Hourani R, El-Hajj T, Barada WH, Hourani M, Yamout BI.
    AJNR Am J Neuroradiol; 2009 May 13; 30(5):936-40. PubMed ID: 19193756
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  • 12. MRI of autosomal dominant pure spastic paraplegia.
    Krabbe K, Nielsen JE, Fallentin E, Fenger K, Herning M.
    Neuroradiology; 1997 Oct 13; 39(10):724-7. PubMed ID: 9351110
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  • 13. Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.
    Sauter SM, Engel W, Neumann LM, Kunze J, Neesen J.
    Hum Mutat; 2004 Jan 13; 23(1):98. PubMed ID: 14695538
    [Abstract] [Full Text] [Related]

  • 14. Hereditary spastic paraplegia.
    Fink JK.
    Neurol Clin; 2002 Aug 13; 20(3):711-26. PubMed ID: 12432827
    [Abstract] [Full Text] [Related]

  • 15. Hereditary spastic paraplegia.
    Murala S, Nagarajan E, Bollu PC.
    Neurol Sci; 2021 Mar 13; 42(3):883-894. PubMed ID: 33439395
    [Abstract] [Full Text] [Related]

  • 16. The extent of axonal loss in the long tracts in hereditary spastic paraplegia.
    Deluca GC, Ebers GC, Esiri MM.
    Neuropathol Appl Neurobiol; 2004 Dec 13; 30(6):576-84. PubMed ID: 15540998
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  • 17. Hereditary spastic paraplegia: genetic heterogeneity and genotype-phenotype correlation.
    Fink JK, Hedera P.
    Semin Neurol; 1999 Dec 13; 19(3):301-9. PubMed ID: 12194386
    [Abstract] [Full Text] [Related]

  • 18. Tract-specific damage at spinal cord level in pure hereditary spastic paraplegia type 4: a diffusion tensor imaging study.
    Navas-Sánchez FJ, Marcos-Vidal L, de Blas DM, Fernández-Pena A, Alemán-Gómez Y, Guzmán-de-Villoria JA, Romero J, Catalina I, Lillo L, Muñoz-Blanco JL, Ordoñez-Ugalde A, Quintáns B, Sobrido MJ, Carmona S, Grandas F, Desco M.
    J Neurol; 2022 Jun 13; 269(6):3189-3203. PubMed ID: 34999956
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