Article metrics
PDF
Other content recommended for you
- Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases
- Transient clinical improvement of a mitochondrial neurogastrointestinal encephalomyopathy-like syndrome after allogeneic haematopoietic stem cell transplantation
- Rare pathogenic mutation in the thymidine phosphorylase gene (TYMP) causing mitochondrial neurogastrointestinal encephalomyelopathy
- The “new” mitochondrial disorders
- Mitochondrial disease: mimics and chameleons
- Recognition, investigation and management of mitochondrial disease
- Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutations
- A young man with bilateral epilepsia intractable and partialis continua
- MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation
- Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies