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Journal Abstract Search

109 related items for PubMed ID: 7285436

  • 1. Heel deformity in hereditary spastic paraplegia.
    Rothschild H, Shoji H, McCormick D.
    Clin Orthop Relat Res; 1981 Oct; (160):48-51. PubMed ID: 7285436
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  • 2. Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia.
    Opjordsmoen S, Nyberg-Hansen R.
    Acta Neurol Scand; 1980 Jan; 61(1):35-41. PubMed ID: 6249060
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  • 7. SCA1 patients may present as hereditary spastic paraplegia and must be included in spastic-ataxias group.
    Pedroso JL, de Souza PV, Pinto WB, Braga-Neto P, Albuquerque MV, Saraiva-Pereira ML, Jardim LB, Barsottini OG.
    Parkinsonism Relat Disord; 2015 Oct; 21(10):1243-6. PubMed ID: 26231471
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  • 8. [A case of complicated form of hereditary spastic paraplegia associated with hypoplasia of the corpus callosum and cataracta].
    Tanaka M, Kobayashi Y, Sato M, Tsuji S.
    Rinsho Shinkeigaku; 1995 Jul; 35(7):798-802. PubMed ID: 8777806
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  • 10. Hereditary spastic paraplegia with hypoplastic corpus callosum in a Turkish family.
    Gucuyener K, Hirfanoglu T, Ok I, Cansu A, Serdaroglu A.
    J Child Neurol; 2007 Feb; 22(2):214-7. PubMed ID: 17621486
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  • 11. [Hereditary spastic paraplegia associated with peripheral neuropathy. Contribution of a family].
    García-Albea E, Peña P, Cabello A, Calandre L.
    Rev Clin Esp; 1979 Jan 31; 152(2):155-9. PubMed ID: 220681
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  • 12. Familial spastic paraplegia, mental retardation, and precocious puberty.
    Raphaelson MI, Stevens JC, Elders J, Comite F, Theodore WH.
    Arch Neurol; 1983 Dec 31; 40(13):809-10. PubMed ID: 6639408
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  • 13. Peroneal somatosensory evoked potentials in the "pure" form of hereditary spastic paraplegia.
    Görke W, Grimm T.
    Neuropediatrics; 1986 Aug 31; 17(3):162-4. PubMed ID: 3762873
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  • 14. [Molecular genetics and gene analysis of hereditary spastic paraplegia].
    Ishiura H.
    Rinsho Shinkeigaku; 2014 Aug 31; 54(12):1016-7. PubMed ID: 25672695
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  • 15. Autosomal recessive spastic paraplegia: evidence for demyelination.
    Rothschild H, Happel L, Rampp D, Hackett E.
    Clin Genet; 1979 Apr 31; 15(4):356-60. PubMed ID: 436332
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  • 16. [A case of autosomal dominant, pure form spastic paraplegia with thinning of the corpus callosum].
    Tomiyasu H, Hayashi R, Watanabe R, Honda M, Yoshii F.
    Rinsho Shinkeigaku; 1998 May 31; 38(5):435-9. PubMed ID: 9805990
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  • 17. Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family.
    Fink JK, Sharp GB, Lange BM, Wu CB, Haley T, Otterud B, Peacock M, Leppert M.
    Neurology; 1995 Feb 31; 45(2):325-31. PubMed ID: 7854534
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  • 18. [Clinical study of familial spastic paraplegia].
    Mukai E, Takahashi A, Matsuo T.
    Rinsho Shinkeigaku; 1987 Nov 31; 27(11):1399-406. PubMed ID: 3447800
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  • 19. The spinal canal in familial spastic paraplegia.
    Vassilopoulos D, Spengos M, Zoumbou V, Scarpalezos S.
    Eur Neurol; 1981 Nov 31; 20(2):110-4. PubMed ID: 7215397
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  • 20. Hereditary spastic paraplegia: identification of an SPG3A gene mutation in a Chinese family.
    Chan KY, Ching CK, Mak CM, Lam CW, Chan AY.
    Hong Kong Med J; 2009 Aug 31; 15(4):304-7. PubMed ID: 19652243
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