Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient

This publication has 29 references indexed in Scilit:

• A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
  Nature, 1990
• Complicated Migraine Studied by Phosphorus Magnetic Resonance Spectroscopy
  Cephalalgia, 1990
• IDENTICAL MITOCHONDRIAL DNA DELETION IN BLOOD AND MUSCLE
  The Lancet, 1989
• A simple method for processing NMR spectra in which acquisition is delayed: Applications to in vivo localized ³¹P NMR spectra acquired using the DRESS technique
  Magnetic Resonance in Medicine, 1988
• Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
  Nature, 1988
• ³¹P magnetization transfer studies of creatine kinase kinetics in living rabbit brain
  Magnetic Resonance in Medicine, 1987
• Mitochondrial myopathies
  Annals of Neurology, 1985
• metabolic recovery after exercise and the assessment of mitochondrial function in Vivo in human skeletal muscle by means of ³¹P NMR
  Magnetic Resonance in Medicine, 1984
• A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
  Analytical Biochemistry, 1983
• Sequence and organization of the human mitochondrial genome
  Nature, 1981