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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

111 related items for PubMed ID: 1876220

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  • 3. 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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  • 6. 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; 44(6):967-71. PubMed ID: 9851444
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  • 7. [Contributions to clinical myology. Ultrasound tomography--a procedure for differential diagnosis].
    von Rohden L, Steinbicker V.
    Psychiatr Neurol Med Psychol Beih; 1987 Dec; 38():141-63. PubMed ID: 3136472
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  • 9. [Quadriceps myopathy as dystrophin-associated myopathy].
    von Mitzlaff HC, Liechti-Gallati S, Rösler KM, Burgunder JM.
    Schweiz Med Wochenschr; 1993 Oct 09; 123(40):1865-9. PubMed ID: 8211039
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  • 10. [Analysis of the polymorphism of primary myopathies with recessive X-linked inheritance].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981 Oct 09; 81(11):1621-4. PubMed ID: 7324662
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  • 11. [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 09; 165(9):1229-41. PubMed ID: 7044494
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  • 15. [A case of familial atypical pseudohypertrophic proximal progressive muscular dystrophy].
    Badalian LO, Temin PA, Arkhipov BA, Zavadenko NN, Bobrova KF, Lysov VL.
    Sov Med; 1989 Dec 09; (9):96-100. PubMed ID: 2603045
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  • 16. Dystrophin or a "related protein" in Duchenne muscular dystrophy?
    Nicholson LV, Johnson MA, Davison K, O'Donnell E, Falkous G, Barron M, Harris JB.
    Acta Neurol Scand; 1992 Jul 09; 86(1):8-14. PubMed ID: 1519480
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  • 19. [Pseudohypertrophic forms of progressive muscular dystrophy with the onset at puberty and a malignant course of the myodystrophic process].
    Badalian LO, Arkhipov BA, Temin PA, Zavadenko NN, Voloshina TG.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988 Jul 09; 88(3):61-4. PubMed ID: 3381616
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  • 20. A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage.
    Rose MR, Howard RS, Genet SA, McMahon CJ, Whitfield A, Morgan-Hughes JA.
    Muscle Nerve; 1993 Jan 09; 16(1):57-62. PubMed ID: 8423832
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