Disease: Visceral myopathy familial external ophthalmoplegia
- A Novel Mutation in an MNGIE Patient Presenting with More Prominent Neurological Symptoms than GI Symptoms
- A very early onset MNGIE-like syndrome with POLG1 mutation and accompanying leukoencephalopathy
- Brain White Matter Lesions and Presumed Crohn's Disease: Did You Consider MNGIE?
- Circulating miRNAs as Biomarkers for Mitochondrial Neuro-Gastrointestinal Encephalomyopathy
- Efficacy of adeno-associated virus gene therapy in a MNGIE murine model enhanced by chronic exposure to nucleosides
- Evidence of enteric angiopathy and neuromuscular hypoxia in patients with mitochondrial neurogastrointestinal encephalomyopathy
- Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 1: peripheral neuropathies
- Hematopoietic stem cell transplantation for mitochondrial neurogastrointestinal encephalopathy: A single-center experience underscoring the multiple factors involved in the prognosis
- Hematopoietic stem cell transplantation with reduced toxicity conditioning regimen in mitochondrial neurogastrointestinal encephalopathy syndrome
- Lysosomal dysfunction and overload of nucleosides in thymidine phosphorylase deficiency of MNGIE
- Mitochondrial neurogastrointestinal encephalomyopathy in a Pakistani female: a case report
- Mitochondrial Neurogastrointestinal Encephalopathy (MNGIE) Disease
- Novel Mutations of the TYMP Gene in Mitochondrial Neurogastrointestinal Encephalomyopathy: Case Series and Literature Review
- POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotype
- Polyneuropathy Reveals Origins of Decade-long Gastrointestinal Symptoms in a Patient With Undiagnosed Mitochondrial Neurogastrointestinal Encephalopathy Caused by a Novel Mutation
- Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes
- Successful Sequential Liver and Isolated Intestine Transplantation for Mitochondrial Neurogastrointestinal Encephalopathy Syndrome: A Case Report
- The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency
- Thymidine Phosphorylase Deficiency or Inhibition Preserves Cardiac Function in Mice With Acute Myocardial Infarction
- Whole exome sequencing reveals two novel compound heterozygous mutations in TWNK as a cause of the hepatocerebral form of mitochondrial DNA depletion syndrome: a case report