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Endothelial dysfunction and platelet hyperactivity in type 2 diabetes mellitus: Molecular insights and therapeutic strategies

If these tests are nondiagnostic, genetic testing for LGMD, more common metabolic myopathies (eg, myophosphorylase, CPT2, myoadenylate deaminase deficiencies), and malignant hyperthermia susceptibility (eg, RYR1 and CACNA1S mutations) is recommended in the appropriate clinical context

Furthermore, sRAGE has been demonstrated to inhibit cellular autophagy through modulation of STAT3-dependent pathways, thereby conferring protection against cardiac ischemia/reperfusion (I/R) injury [60]

Jul 6 2010;130(1):93-97

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