Share
PDF
Other content recommended for you
- Transient clinical improvement of a mitochondrial neurogastrointestinal encephalomyopathy-like syndrome after allogeneic haematopoietic stem cell transplantation
- The neurology of enteric disease
- Epilepsy in a patient with ataxia caused by vitamin E deficiency
- MNGIE with lack of skeletal muscle involvement and a novel TP splice site mutation
- Mitochondrial neurogastrointestinal encephalopathy disease (MNGIE)
- The management of adult patients with severe chronic small intestinal dysmotility
- Rare pathogenic mutation in the thymidine phosphorylase gene (TYMP) causing mitochondrial neurogastrointestinal encephalomyelopathy
- Disorders of the spinal cord and roots
- Ataxia with isolated vitamin E deficiency presenting as mutation negative Friedreich’s ataxia
- Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases