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Journal Abstract Search

155 related items for PubMed ID: 6530360

  • 1. Detection of myopathies in children by 1H nuclear magnetic resonance (NMR) and comparison with histopathological patterns.
    Scelsi R, Savoldi F, Borghi L, Villa M.
    Ital J Neurol Sci; 1984 Dec; 5(4):381-4. PubMed ID: 6530360
    [Abstract] [Full Text] [Related]

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  • 3. Central core disease--a congenital myopathy.
    Saper JR, Itabashi HH.
    Dis Nerv Syst; 1976 Nov; 37(11):649-53. PubMed ID: 991722
    [Abstract] [Full Text] [Related]

  • 4. Muscular dystrophies and other genetic myopathies.
    Shieh PB.
    Neurol Clin; 2013 Nov; 31(4):1009-29. PubMed ID: 24176421
    [Abstract] [Full Text] [Related]

  • 5. Magnetic resonance imaging of primary skeletal muscle diseases: patterns of distribution and severity of involvement.
    Lamminen AE.
    Br J Radiol; 1990 Dec; 63(756):946-50. PubMed ID: 2268764
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  • 6. High-frequency ultrasonography of skeletal muscle in children with neuromuscular disease.
    Lamminen A, Jääskeläinen J, Rapola J, Suramo I.
    J Ultrasound Med; 1988 Sep; 7(9):505-9. PubMed ID: 3054144
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  • 7. Topical magnetic resonance for the study of muscle metabolism in human myopathy.
    Edwards RH, Griffiths RD, Cady EB.
    Clin Physiol; 1985 Apr; 5(2):93-109. PubMed ID: 3995881
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  • 8. Myopathies.
    Glasberg MR.
    Neurosurgery; 1979 Dec; 5(6):747-58. PubMed ID: 392333
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  • 9. [Muscular magnetic resonance imaging for evaluation of myopathies in children].
    Peters SA, Köhler C, Schara U, Hohendahl J, Vorgerd M, Nicolas V, Heyer CM.
    Klin Padiatr; 2008 Dec; 220(1):37-46. PubMed ID: 18098096
    [Abstract] [Full Text] [Related]

  • 10. Pathology of the muscular dystrophies and the congenital nonprogressive myopathies.
    Armbrustmacher VW.
    Pathol Annu; 1980 Dec; 15(Pt 1):301-33. PubMed ID: 7443308
    [No Abstract] [Full Text] [Related]

  • 11. [Histopathological aspects of progressive muscular dystrophies. The place of classical histological techniques in their diagnosis].
    Escourolle R, Fardeau M.
    Ann Anat Pathol (Paris); 1973 Dec; 18(1):109-37. PubMed ID: 4577474
    [No Abstract] [Full Text] [Related]

  • 12. Ultrastructure of skeletal muscle in muscular dystrophy, the carrier state and other human myopathies.
    Papadimitriou JM, Kakulas BA.
    Proc Aust Assoc Neurol; 1968 Dec; 5(1):87-94. PubMed ID: 5250033
    [No Abstract] [Full Text] [Related]

  • 13. Magnetic resonance of diseased skeletal muscle: combined T1 measurement and chemical shift imaging.
    Lamminen AE, Tanttu JI, Sepponen RE, Suramo IJ, Pihko H.
    Br J Radiol; 1990 Aug; 63(752):591-6. PubMed ID: 2400872
    [Abstract] [Full Text] [Related]

  • 14. Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining.
    Connolly AM, Pestronk A, Planer GJ, Yue J, Mehta S, Choksi R.
    Neurology; 1996 Mar; 46(3):810-14. PubMed ID: 8618688
    [Abstract] [Full Text] [Related]

  • 15. Autosomal dominant centronuclear myopathy: report of a new family with clinical features simulating facioscapulohumeral syndrome.
    Felice KJ, Grunnet ML.
    Muscle Nerve; 1997 Sep; 20(9):1194-6. PubMed ID: 9270681
    [Abstract] [Full Text] [Related]

  • 16. Muscle fiber degeneration and necrosis in muscular dystrophy and other muscle diseases: cytochemical and immunocytochemical data.
    Cornelio F, Dones I.
    Ann Neurol; 1984 Dec; 16(6):694-701. PubMed ID: 6524876
    [Abstract] [Full Text] [Related]

  • 17. MR imaging of primary skeletal muscle diseases in children.
    Chan WP, Liu GC.
    AJR Am J Roentgenol; 2002 Oct; 179(4):989-97. PubMed ID: 12239053
    [No Abstract] [Full Text] [Related]

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  • 20. Distal myopathies and dystrophies.
    Barohn RJ.
    Semin Neurol; 1993 Sep; 13(3):247-55. PubMed ID: 8272595
    [No Abstract] [Full Text] [Related]

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