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PUBMED FOR HANDHELDS

Journal Abstract Search

123 related items for PubMed ID: 7441281

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  • 2. Familial spastic paraplegia, peroneal neuropathy, and crural hypopigmentation: a new neurocutaneous syndrome.
    Stewart RM, Tunell G, Ehle A.
    Neurology; 1981 Jun; 31(6):754-7. PubMed ID: 6264350
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  • 3. Progressive spastic paraparesis, vitiligo, premature graying, and distinct facial appearance: a new genetic syndrome in 3 sibs.
    Lison M, Kornbrut B, Feinstein A, Hiss Y, Boichis H, Goodman RM.
    Am J Med Genet; 1981 Jun; 9(4):351-7. PubMed ID: 7294071
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  • 6. [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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  • 8. [Familial spastic paraplegia with amyotrophy. Clinical, electromyographic, histochemical study and microdissection].
    Werneck LC, Sanches MC.
    Arq Neuropsiquiatr; 1979 Jun 31; 37(2):138-50. PubMed ID: 91360
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  • 9. Hereditary sensory neuropathy with spastic paraplegia.
    Cavanagh NP, Eames RA, Galvin RJ, Brett EM, Kelly RE.
    Brain; 1979 Mar 31; 102(1):79-94. PubMed ID: 218673
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  • 12. Hereditary distal dominant amyotrophy followed by spastic paraplegia.
    Sunohara N, Tomi H, Kishibayashi J, Mukoyama M.
    Intern Med; 1993 Nov 31; 32(11):825-31. PubMed ID: 8012082
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  • 13. Spastic paraplegia, glaucoma and mental retardation--in three siblings. A new genetic syndrome.
    Heijbel J, Jagell S.
    Hereditas; 1981 Nov 31; 94(2):203-7. PubMed ID: 7298353
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  • 14. Four brothers with mental retardation, spastic paraplegia and palmoplantar hyperkeratosis. A new syndrome?
    Fitzsimmons JS, Fitzsimmons EM, McLachlan JI, Gilbert GB.
    Clin Genet; 1983 Apr 31; 23(4):329-35. PubMed ID: 6221837
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  • 19. Adrenomyeloneuropathy--clinical and biochemical diagnosis.
    Berkovic SF, Zajac JD, Warburton DJ, Merory JR, Fellenberg AJ, Poulos A, Pollard AC.
    Aust N Z J Med; 1983 Dec 31; 13(6):594-600. PubMed ID: 6326727
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