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Journal Abstract Search

117 related items for PubMed ID: 7117711

  • 1. Heredofamilial syndrome of spastic paraplegia, dysarthria and cutaneous lesions in ive siblings.
    Bahemuka M, Brown JD.
    Dev Med Child Neurol; 1982 Aug; 24(4):519-24. PubMed ID: 7117711
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  • 2. Familial spastic paraplegia with Kallmann's syndrome.
    Tuck RR, O'Neill BP, Gharib H, Mulder DW.
    J Neurol Neurosurg Psychiatry; 1983 Jul; 46(7):671-4. PubMed ID: 6604133
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  • 3. Familial spastic paraplegia, mental retardation, and precocious puberty.
    Raphaelson MI, Stevens JC, Elders J, Comite F, Theodore WH.
    Arch Neurol; 1983 Dec; 40(13):809-10. PubMed ID: 6639408
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  • 4. Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or "new" syndrome.
    Neuhäuser G, Wiffler C, Opitz JM.
    Clin Genet; 1976 Mar; 9(3):315-23. PubMed ID: 1261070
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  • 5. 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; 23(4):329-35. PubMed ID: 6221837
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  • 6. Familial spastic paraplegia on Mitiaro, Cook Islands.
    Kuberski T, Tetava P, Koteka G.
    N Z Med J; 1981 Mar 25; 93(680):187-8. PubMed ID: 6941104
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  • 7. [Familial spastic paraplegia. Genetic-scientific discussion apropos of an affected family].
    Gonçalves A.
    Arq Neuropsiquiatr; 1980 Jun 25; 38(2):144-9. PubMed ID: 7436797
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  • 11. 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 25; 9(4):351-7. PubMed ID: 7294071
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  • 12. Spastic paraplegia, glaucoma and mental retardation--in three siblings. A new genetic syndrome.
    Heijbel J, Jagell S.
    Hereditas; 1981 Jun 25; 94(2):203-7. PubMed ID: 7298353
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  • 13. [Familial spastic paraplegia in 3 families].
    Fujiwara H, Akabori O, Akashi K, Moriya S.
    Seikei Geka; 1971 Jun 25; 22(6):471-6. PubMed ID: 5104423
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  • 16. [FAMILIAL SPASTIC PARAPLEGIA OF THE TYPE STRUMPELL-LORRAIN IN 3 SISTERS DAUGHTERS OF A CONSANGUINOUS MARRIAGE].
    GOMEZ MALARET S, LATUFF H, CHOMPREDEPENA L.
    Arch Pediatr Urug; 1963 Nov 25; 34():673-8. PubMed ID: 14123546
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  • 19. Slowly progressive autosomal dominant spastic paraplegia with late onset, variable expression and reduced penetrance: a basis for diagnosis and counseling.
    Burdick AB, Owens LA, Peterson CR.
    Clin Genet; 1981 Jan 25; 19(1):1-7. PubMed ID: 7460376
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