Mitochondrial encephalomyopathies are a group of multisystemic disorders that caused by Mitochondrial DNA or nuclear mutations to result in disturbance of mitochondrial Structures and function, which involve central nervous system and muscle mainly.

Clinical,imaging and pathological features of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(report of 1 case)

Analysis of two mitochondrial encephalomyopathy cases on clinical、image and pathology

Chronic progressive external ophthalmoplegia type of mitochondrial myopathy(report of 3 families);

Mitochondrial DNA mutation analysis in patients with mitochondrial myopathy;

Mitochondrial myopathy and mitochondrial encephalomyopathy;