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. 1970 May;63(5):470–474. doi: 10.1177/003591577006300527

The value of electron microscopy in muscle biopsies.

P Hudgson
PMCID: PMC1811779  PMID: 5271562

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Behrman S. Pathology of papilloedema. Brain. 1966 Mar;89(1):1–14. doi: 10.1093/brain/89.1.1. [DOI] [PubMed] [Google Scholar]
  2. Bradley W. G., Hudgson P., Gardner-Medwin D., Walton J. N. Myopathy associated with abnormal lipid metabolism in skeletal muscle. Lancet. 1969 Mar 8;1(7593):495–498. doi: 10.1016/s0140-6736(69)91593-1. [DOI] [PubMed] [Google Scholar]
  3. Bradley W. G. Ultrastructural changes in adynamia episodica hereditaria and normokalaemic familial periodic paralysis. Brain. 1969;92(2):379–390. doi: 10.1093/brain/92.2.379. [DOI] [PubMed] [Google Scholar]
  4. COPENHAVER W. M., MOORE D. H., RUSKA H. Electron microscopic and histochemical observations of muscle degeneration after tourniquet. J Biophys Biochem Cytol. 1956 Nov 25;2(6):755–764. doi: 10.1083/jcb.2.6.755. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Campbell M. J., Rebeiz J. J., Walton J. N. Myotubular, centronuclear or Peri-Centronuclear myopathy? J Neurol Sci. 1969 May-Jun;8(3):425–443. doi: 10.1016/0022-510x(69)90003-3. [DOI] [PubMed] [Google Scholar]
  6. Coleman R. F., Nienhuis A. W., Brown W. J., Munsat T. L., Pearson C. M. New myopathy with mitochondrial enzyme hyperactivity. Histochemical demonstration. JAMA. 1967 Feb 27;199(9):624–630. [PubMed] [Google Scholar]
  7. Drachman D. B., Murphy S. R., Nigam M. P., Hills J. R. "Myopathic" changes in chronically denervated muscle. Arch Neurol. 1967 Jan;16(1):14–24. doi: 10.1001/archneur.1967.00470190018002. [DOI] [PubMed] [Google Scholar]
  8. Gonatas N. K., Shy G. M., Godfrey E. H. Nemaline myopathy. The origin of nemaline structures. N Engl J Med. 1966 Mar 10;274(10):535–539. doi: 10.1056/NEJM196603102741002. [DOI] [PubMed] [Google Scholar]
  9. Hudgson P., Gardner-Medwin D., Fulthorpe J. J., Walton J. N. Nemaline myopathy. Neurology. 1967 Dec;17(12):1125–1142. doi: 10.1212/wnl.17.12.1125. [DOI] [PubMed] [Google Scholar]
  10. Hudgson P., Gardner-Medwin D., Worsfold M., Pennington R. J., Walton J. N. Adult myopathy from glycogen storage disease due to acid maltase deficiency. Brain. 1968 Sep;91(3):435–462. doi: 10.1093/brain/91.3.435. [DOI] [PubMed] [Google Scholar]
  11. Hudgson P., Pearce G. W., Walton J. N. Pre-clinical muscular dystrophy: histopathological changes observed on muscle biopsy. Brain. 1967 Sep;90(3):565–576. doi: 10.1093/brain/90.3.565. [DOI] [PubMed] [Google Scholar]
  12. LUFT R., IKKOS D., PALMIERI G., ERNSTER L., AFZELIUS B. A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study. J Clin Invest. 1962 Sep;41:1776–1804. doi: 10.1172/JCI104637. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. MAGEE K. R., SHY G. M. A new congenital non-progressive myopathy. Brain. 1956 Dec;79(4):610–621. doi: 10.1093/brain/79.4.610. [DOI] [PubMed] [Google Scholar]
  14. PRICE H., PEASE D. C., PEARSON C. M. Selective actin filament and Z-band degeneration induced by plasmocid. An electron microscopic study. Lab Invest. 1962 Jul;11:549–562. [PubMed] [Google Scholar]
  15. Pearce G. W. Electron microscopy in the study of muscular dystrophy. Ann N Y Acad Sci. 1966 Sep 9;138(1):138–150. doi: 10.1111/j.1749-6632.1966.tb41162.x. [DOI] [PubMed] [Google Scholar]
  16. Price H. M., Gordon G. B., Pearson C. M., Munsat T. L., Blumberg J. M. New evidence for excessive accumulation of Z-band material in nemaline myopathy. Proc Natl Acad Sci U S A. 1965 Nov;54(5):1398–1406. doi: 10.1073/pnas.54.5.1398. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. SHY G. M., ENGEL W. K., SOMERS J. E., WANKO T. NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY. Brain. 1963 Dec;86:793–810. doi: 10.1093/brain/86.4.793. [DOI] [PubMed] [Google Scholar]
  18. Shafiq S. A., Milhorat A. T., Gorycki M. A. Fine structure of human muscle in neurogenic atrophy. Neurology. 1967 Oct;17(10):934–948. doi: 10.1212/wnl.17.10.934. [DOI] [PubMed] [Google Scholar]
  19. Spiro A. J., Shy G. M., Gonatas N. K. Myotubular myopathy. Persistence of fetal muscle in an adolescent boy. Arch Neurol. 1966 Jan;14(1):1–14. doi: 10.1001/archneur.1966.00470070005001. [DOI] [PubMed] [Google Scholar]
  20. van Wijngaarden G. K., Bethlem J., Meijer A. E., Hülsmann W. C., Feltkamp C. A. Skeletal muscle disease with abnormal mitochondria. Brain. 1967 Sep;90(3):577–592. doi: 10.1093/brain/90.3.577. [DOI] [PubMed] [Google Scholar]

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