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Journal Abstract Search

93 related items for PubMed ID: 3136472

  • 1. [Contributions to clinical myology. Ultrasound tomography--a procedure for differential diagnosis].
    von Rohden L, Steinbicker V.
    Psychiatr Neurol Med Psychol Beih; 1987; 38():141-63. PubMed ID: 3136472
    [No Abstract] [Full Text] [Related]

  • 2. [Significance of dystrophin analysis in adult myopathies. Study methods, case reports and current pathogenetic considerations].
    Gold R, Kress W, Meurers B, Müller CR, Reichmann H.
    Nervenarzt; 1991 Jun; 62(6):360-8. PubMed ID: 1876220
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  • 4. The new genetics and its application in the study of childhood muscular dystrophies.
    Chakravarty A, Chatterjee S.
    J Assoc Physicians India; 1991 Dec; 39(12):943-8. PubMed ID: 1816224
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  • 7. [Current concepts of X-linked myopathies and social consequences of their diagnosis (apropos of 88 cases)].
    Serratrice G, Cros D, Pellissier JF, Pouget J.
    Bull Acad Natl Med; 1981 Dec; 165(9):1229-41. PubMed ID: 7044494
    [No Abstract] [Full Text] [Related]

  • 8. Carrier detection in X-linked muscular dystrophy.
    Walton JN.
    J Genet Hum; 1969 Oct; 17(3):497-510. PubMed ID: 5387424
    [No Abstract] [Full Text] [Related]

  • 9. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
    Spiegler AW, Huppert P, Werner W, Metzke H, Strobel U, Köhler K, Gerhardt R, Kaufmann J, Herrmann FH.
    Z Arztl Fortbild (Jena); 1988 Oct; 82(22):1139-42. PubMed ID: 3247797
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  • 11. [Muscular disease of X-linked autosomal recessive transmission with early muscular retractions and cardiac conduction disorders].
    Serratrice G, Pouget J, Pellissier JF, Gastaut JL, Cros D.
    Rev Neurol (Paris); 1982 Oct; 138(10):713-24. PubMed ID: 6891495
    [No Abstract] [Full Text] [Related]

  • 12. Facioscapulohumeral muscular dystrophy: the choice of a biopsy site.
    Bodensteiner JB, Schochet SS.
    Muscle Nerve; 1986 Oct; 9(6):544-7. PubMed ID: 3736585
    [Abstract] [Full Text] [Related]

  • 13. [Analysis of the polymorphism of primary myopathies with recessive X-linked inheritance].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981 Oct; 81(11):1621-4. PubMed ID: 7324662
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  • 15. [Heredity of myopathy, with special reference to progressive muscular dystrophy].
    Sugita H.
    Naika; 1970 Apr; 25(4):611-9. PubMed ID: 4912548
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  • 16. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.
    Jackson CE, Strehler DA.
    Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795
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  • 18. Duchenne's muscular dystrophy: carrier detection by imaging technics.
    Rott HD, Rödl W, Santellani M, Nebel G.
    J Genet Hum; 1984 Sep; 32(4):287-90. PubMed ID: 6387044
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  • 19. [Different phenotypes of type IXb glycogenosis (phosphorylase-b-kinase deficiency) in adult- and early childhood].
    Müller P, Bührdel P, Freidt B, Böhme HJ.
    Med Klin (Munich); 1996 Oct 15; 91(10):667-9. PubMed ID: 9019646
    [No Abstract] [Full Text] [Related]

  • 20. Duchenne's muscular dystrophy: carrier detection by muscle ultrasound.
    Rott HD, Mulz D.
    J Genet Hum; 1983 Mar 15; 31(1):63-5. PubMed ID: 6619807
    [No Abstract] [Full Text] [Related]

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