All Stories

  1. Mitochondrial ataxia is genetically and phenotypically heterogeneous
  2. Retinal involvement in m.3243A>G carriers
  3. Frequency of Headache in Mitochondrial Disorders
  4. Comment on “Role of Mitochondrial Genome Mutations in Pathogenesis of Carotid Atherosclerosis”
  5. Mitochondrial multiorgan disorder syndrome score generated from definite mitochondrial disorders
  6. Reduced Bone Mineral Density in m.3243A>G Carriers May Be Multifactorial
  7. Can MR spectroscopy and muscle biopsy findings be correlated with MELAS and CPEO?
  8. POLG1 mutations in bipolar disorders
  9. Psychological morbidity in Leber’s hereditary optic neuropathy depends on phenotypic, social, economic, and genetic factors
  10. Regional cerebral hyperperfusion: A biomarker of upcoming stroke-like episodes?
  11. Phenotypic and genotypic features in pediatric and adult mitochondrial disorders
  12. Leber’s hereditary optic neuropathy is multiorgan not mono-organ