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Facial weakness in hereditary inclusion body myopathies.
Argov Z, Sadeh M, Eisenberg I, Karpati G, Mitrani-Rosenbaum S. Argov Z, et al. Neurology. 1998 Jun;50(6):1925-6. doi: 10.1212/wnl.50.6.1925. Neurology. 1998. PMID: 9633772 No abstract available.
Genetics of inclusion body myopathies.
Argov Z, Eisenberg I, Mitrani-Rosenbaum S. Argov Z, et al. Curr Opin Rheumatol. 1998 Nov;10(6):543-7. doi: 10.1097/00002281-199811000-00006. Curr Opin Rheumatol. 1998. PMID: 9812214 Review.
The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy.
Hinderlich S, Salama I, Eisenberg I, Potikha T, Mantey LR, Yarema KJ, Horstkorte R, Argov Z, Sadeh M, Reutter W, Mitrani-Rosenbaum S. Hinderlich S, et al. Among authors: argov z. FEBS Lett. 2004 May 21;566(1-3):105-9. doi: 10.1016/j.febslet.2004.04.013. FEBS Lett. 2004. PMID: 15147877 Free article.
173 results