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Journal Abstract Search

119 related items for PubMed ID: 4538352

  • 1. [Significance of sibship studies--as demonstrated on a new family with neural muscular atrophy (Charcot-Marie-Tooth)].
    Wagner A.
    Z Arztl Fortbild (Jena); 1972 Jun 15; 66(12):621-4. PubMed ID: 4538352
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  • 6. Pathogenesis of Charcot-Marie-Tooth disease. Gait analysis and electrophysiologic, genetic, histopathologic, and enzyme studies in a kinship.
    Sabir M, Lyttle D.
    Clin Orthop Relat Res; 1984 Apr 15; (184):223-35. PubMed ID: 6705352
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  • 9. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease].
    Câmpeanu E, Morariu M.
    Rev Roum Neurol; 1970 Apr 15; 7(1):47-56. PubMed ID: 5527990
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  • 15. [2 cases of hereditary progressive muscular atrophy of Charcot-Marie-Tooth type].
    Milosavljević I, Pavićević R, Jekić B.
    Med Glas; 1970 Feb 15; 24(2):73-7. PubMed ID: 5204405
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  • 19. [Charcot-Marie-Tooth disease with early onset. Presentation of a family].
    Zellweger H, Schochet SS, Pavone L, Bodensteiner J.
    Pediatria (Napoli); 1971 Feb 15; 79(2):198-214. PubMed ID: 5095773
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  • 20. [Involvement of the optic nerve in neural muscular atrophy].
    Reisecker F, Leblhuber F, Deisenhammer E.
    Wien Klin Wochenschr; 1985 Aug 30; 97(16):658-61. PubMed ID: 4060727
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