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Journal Abstract Search

100 related items for PubMed ID: 13870897

  • 1. [Considerations on an atypical case of the Roussy-Levy syndrome].
    BONARETTI T, SARAVAL A.
    Osp Psichiatr; 1960; 28():266-78. PubMed ID: 13870897
    [No Abstract] [Full Text] [Related]

  • 2. [Progressive ataxia and distal muscular atrophy--differential diagnostic considerations on Roussy-Lévy syndrome].
    Aksu F, Christen HJ, Hanefeld F.
    Klin Padiatr; 1986; 198(2):114-8. PubMed ID: 3702272
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  • 4. [A family with Roussy-Levy syndrome].
    HAYNAL A, REGLI F.
    Confin Neurol; 1962; 22():128-40. PubMed ID: 13963587
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  • 6. [Comments on Roussy-Levy syndrome].
    GARCIA-CASTRILLO SANCHEZ L, ORDEIG PASTELLS F.
    Medicina (Madr); 1951 Jun; 19(6):477-84. PubMed ID: 14862700
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  • 7. [Study of hereditary areflexic dystasia; present condition of four of the first seven cases of Roussy and Mlle. Lévy thirty years after the first publication of these authors].
    LAPRESLE J.
    Sem Hop; 1951 Jun; 32(44-45):2473-82. PubMed ID: 13360305
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  • 8. [Clinical contribution to the knowledge of the forms of passage or of association between Friedreich's disease and Charcot-Marie-Tooth amyotrophy].
    URAS A, GAGGINO G.
    Rass Med Sarda; 1960 Jun; 62():203-14. PubMed ID: 13840430
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  • 13. Data on three of the original patients of Roussy and Levy (1926).
    Salisachs P, Findley LJ, Codina M, La Torre P, Martinez-Lage JM.
    Muscle Nerve; 1982 Oct; 5(8):663-4. PubMed ID: 7155179
    [No Abstract] [Full Text] [Related]

  • 14. A case of the Roussy-Levy syndrome family.
    Bartosik-Psujek H, Stelmasiak Z.
    Ann Univ Mariae Curie Sklodowska Med; 2001 Oct; 56():393-5. PubMed ID: 11977346
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  • 17. Familial peroneal muscular atrophy and its association with the familial ataxias and tremor and longevity.
    HIERONS R.
    J Neurol Neurosurg Psychiatry; 1956 May; 19(2):155-60. PubMed ID: 13346390
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  • 18. [Roussy-Lévy disease].
    PINTUS G.
    Riv Patol Nerv Ment; 1950 May; 71(1):179-81. PubMed ID: 15441985
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  • 19. [SYNDROME OF SPINO-CEREBELLAR DEGENERATION WITH OPTIC ATROPHY AND DISTAL AMYOTROPHY OF THE CHARCOT-MARIE-TOOTH TYPE IN A 4-YEAR-OLD CHILD].
    BERNARD R, MOUREN P, SOULAYROL R, PINSARD N.
    Pediatrie; 1963 May; 18():816-21. PubMed ID: 14106624
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  • 20. [Autopsy case of Charcot-Marie-Tooth disease with optic nerve atrophy and degeneration of the spinal tract. A family with muscular atrophy, ataxia, retinal degeneration and diabetes mellitus].
    Oguchi K, Tsubaki T, Ikuta F.
    Rinsho Shinkeigaku; 1977 Jan; 17(1):52-7. PubMed ID: 557401
    [No Abstract] [Full Text] [Related]

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