Altered Thymidine Metabolism Due to Defects of Thymidine Phosphorylase

This publication has 29 references indexed in Scilit:

• Mitochondrial encephalomyopathies: Gene Mutation
  Neuromuscular Disorders, 2001
• Mitochondrial neurogastrointestinal encephalomyopathy: An autosomal recessive disorder due to thymidine phosphorylase mutations
  Annals of Neurology, 2000
• Mitochondrial encephalomyopathies: Back to mendelian genetics
  Annals of Neurology, 1999
• Thymidine Phosphorylase Gene Mutations in MNGIE, a Human Mitochondrial Disorder
  Science, 1999
• Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome
  Neurology, 1998
• Thymidine phosphorylase, 2-deoxy-D-ribose and angiogenesis
  Biochemical Journal, 1998
• Mitochondria in neuromuscular disorders
  Biochimica et Biophysica Acta (BBA) - Bioenergetics, 1998
• Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome Maps to Chromosome 22q13.32-qter
  American Journal of Human Genetics, 1998
• Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
  Nature Genetics, 1995
• Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)
  Neurology, 1994