Colchicine myopathy in a case of familial mediterranean fever: immunohistochemical and ultrastructural study of accumulated tubulin-immunoreactive material-Reference-Cited by-同舟云学术

Colchicine myopathy in a case of familial mediterranean fever: immunohistochemical and ultrastructural study of accumulated tubulin-immunoreactive material

Published:1992 Issue:4 Volume:83 Page:440-444
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Himmelmann F.,Schr�der J. M.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF00713539.pdf

Reference16 articles.

1. Barakat MH, Karnik AM, Majeed HWA, El-Sobki NI, Fenech FF (1986) Familial mediterranean fever (recurrent hereditary polyserositis) in arabs. A study of 175 patients and review of the literature. Q J Med 60:837?847

2. Bischoff R, Holtzer H (1968) The effect of mitotic inhibitors on myogenesis in vitro. J Cell Biol 36:111?127

3. Bitar E, Salibra G (1988) Les manifestations musculaires de la maladie périodique. Rev Rhum Mal Osteoartic 55:261?263

4. Cook GC (1986) Periodic disease, recurrent polyserositis, familial mediterranean fever, or simply ?FMF?. Q J Med 60(233):819?823

5. Fardeau M, Tomé F (1981) Non-neoplastic disorders of skeletal muscle. In: Johannensen JV (ed) Electron microscopy in Human Medicine, vol 4; Soft tissues, bones and joints. McGraw-Hill, New York, pp 257?319

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