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PUBMED FOR HANDHELDS

Journal Abstract Search


206 related items for PubMed ID: 7324662

  • 1. [Analysis of the polymorphism of primary myopathies with recessive X-linked inheritance].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981; 81(11):1621-4. PubMed ID: 7324662
    [Abstract] [Full Text] [Related]

  • 2. [Clinical polymorphism of X-linked myopathies].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974; 74(3):321-9. PubMed ID: 4466264
    [No Abstract] [Full Text] [Related]

  • 3. [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
    [No Abstract] [Full Text] [Related]

  • 4. [Identification of the carrier state in the severe recessive X-linked muscular dystrophy (Duchenne type). I. Assay of activated serum creatine kinase activity in serum (author's transl)].
    Rotthauwe HW, Kowalewski S.
    Z Kinderheilkd; 1973 Nov 19; 115(4):333-42. PubMed ID: 4591596
    [No Abstract] [Full Text] [Related]

  • 5. Hereditary myopathies.
    Emery AE.
    Clin Orthop Relat Res; 1964 Nov 19; 33():164-73. PubMed ID: 5889019
    [No Abstract] [Full Text] [Related]

  • 6. [Pseudohypertrophic proximal progressive muscular dystrophy with a malignant course manifesting itself in adolescence].
    Badalian LO, Temin PA, Saidbegov DG, Nikitin MV, Arkhipov BA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1989 Nov 19; 89(3):113-20. PubMed ID: 2728733
    [Abstract] [Full Text] [Related]

  • 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 19; 165(9):1229-41. PubMed ID: 7044494
    [No Abstract] [Full Text] [Related]

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  • 9. [A family of scapula-back type of x-linked recessive muscular dystrophy].
    Ji XW.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun 19; 22(3):136-8, 190. PubMed ID: 2591265
    [Abstract] [Full Text] [Related]

  • 10. [Correlations between clinical and muscle-morphological (histochemical and electron microscopic) characteristics in X-linked myopathies].
    Laszló A, Zombori J, Halász J, Mészáros M.
    Orv Hetil; 1986 Aug 10; 127(32):1943-7. PubMed ID: 3763207
    [No Abstract] [Full Text] [Related]

  • 11. [Principal aspects of research in primary myopathies with the recessive X-linked type of inheritance (review)].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 Aug 10; 82(4):124-33. PubMed ID: 7046305
    [No Abstract] [Full Text] [Related]

  • 12. The new genetics and its application in the study of childhood muscular dystrophies.
    Chakravarty A, Chatterjee S.
    J Assoc Physicians India; 1991 Dec 10; 39(12):943-8. PubMed ID: 1816224
    [No Abstract] [Full Text] [Related]

  • 13. Muscle fiber immaturity and inactivity reduce myonecrosis in Duchenne muscular dystrophy.
    Kimura S, Sugino S, Ohtani Y, Matsukura M, Nishino I, Ikezawa M, Sakata A, Kondo Y, Yoshioka K, Huard J, Nonaka I, Miike T.
    Ann Neurol; 1998 Dec 10; 44(6):967-71. PubMed ID: 9851444
    [Abstract] [Full Text] [Related]

  • 14. [Clinical picture of X chromosome recessive ichthyosis].
    Voss M.
    Dermatol Monatsschr; 1985 Dec 10; 171(1):25-37. PubMed ID: 4038949
    [No Abstract] [Full Text] [Related]

  • 15. [Contributions to clinical myology. Ultrasound tomography--a procedure for differential diagnosis].
    von Rohden L, Steinbicker V.
    Psychiatr Neurol Med Psychol Beih; 1987 Dec 10; 38():141-63. PubMed ID: 3136472
    [No Abstract] [Full Text] [Related]

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  • 19. [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 Dec 10; 138(10):713-24. PubMed ID: 6891495
    [No Abstract] [Full Text] [Related]

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