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PUBMED FOR HANDHELDS

Journal Abstract Search


189 related items for PubMed ID: 7182095

  • 1. [Familial spastic paraplegia associated with large stature and chromosomal abnormalities].
    Tanaka M, Uchiyama T, Komatsu M, Morimatsu M, Hirai S.
    Rinsho Shinkeigaku; 1982 Oct; 22(10):940-6. PubMed ID: 7182095
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  • 4. [Juvenile autosomal-recessive spastic paraplegia].
    Badalian LO, Iadgarov IS, Arkhipov BA, Temin PA, Bulaeva NV.
    Pediatriia; 1989 Oct; (2):90-2. PubMed ID: 2726376
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  • 11. Hereditary spastic paraplegia. A diagnostic reminder.
    Gordon N.
    Dev Med Child Neurol; 1993 May; 35(5):452-5. PubMed ID: 8495827
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  • 12. [Two siblings with familial spastic paraplegia associated with decreased levels of factor XII].
    Fujii K, Sadoshima S, Kusuda K, Shirouzu A, Fujishima M.
    Rinsho Shinkeigaku; 1986 Aug; 26(8):851-5. PubMed ID: 3802679
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  • 14. [Clinical study of familial spastic paraplegia].
    Mukai E, Takahashi A, Matsuo T.
    Rinsho Shinkeigaku; 1987 Nov; 27(11):1399-406. PubMed ID: 3447800
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  • 15. [Complicated spastic paraplegia with sex-linked inheritance (report of a family)].
    Galassi G, Penne A, Colombo A, Forabosco A.
    Acta Neurol (Napoli); 1977 Nov; 32(6):746-56. PubMed ID: 605830
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  • 17. The late form of pure familial spastic paraplegia.
    Vernea J, Symington GR.
    Clin Exp Neurol; 1977 Nov; 14():37-41. PubMed ID: 358187
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  • 18. [Familial spastic paraplegia occurring in siblings].
    Ogawa A, Shiohira A.
    Nihon Shonika Gakkai Zasshi; 1965 Oct; 69(10):884-8. PubMed ID: 5894648
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  • 20. Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1).
    Wiktor A, Van Dyke DL, Weiss L.
    Am J Med Genet; 1993 Jan 01; 45(1):22-4. PubMed ID: 8418653
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