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Journal of the Neurological Sciences|April 1, 1996
Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defectG M Fabrizi, R Lodi, M D'Ettorre, et al.Journal of Neurology|July 1, 1995
Lipoic (thioctic) acid increases brain energy availability and skeletal muscle performance as shown by in vivo 31P-MRS in a patient with mitochondrial cytopathyB Barbiroli, R Medori, H J Tritschler, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 23, 2002
Phosphorus MR spectroscopy shows a tissue specific in vivo distribution of biochemical expression of the G3460A mutation in Leber's hereditary optic neuropathyR Lodi, V Carelli, P Cortelli, et al.Molecular Aspects of Medicine|January 1, 1994
The use of phosphorus magnetic resonance spectroscopy to study in vivo the effect of coenzyme Q10 treatment in retinitis pigmentosaR Lodi, S Iotti, L Scorolli, et al.Neurology|March 10, 2004
Diffusion MRI shows increased water apparent diffusion coefficient in the brains of cirrhoticsR Lodi, C Tonon, A Stracciari, et al.Journal of Neurology|March 1, 1994
Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopyG Vita, A Toscano, N Bresolin, et al.Neurology|August 1, 1991
Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian familyP Cortelli, P Montagna, P Avoni, et al.Neurology|July 1, 1995
Defective brain and muscle energy metabolism shown by in vivo 31P magnetic resonance spectroscopy in nonaffected carriers of 11778 mtDNA mutationB Barbiroli, P Montagna, P Cortelli, et al.Pediatric Research|December 13, 1997
Deficit of brain and skeletal muscle bioenergetics and low brain magnesium in juvenile migraine: an in vivo 31P magnetic resonance spectroscopy interictal studyR Lodi, P Montagna, S Soriani, et al.Journal of the Neurological Sciences|April 1, 1995
Epilepsia partialis continua associated with NADH-coenzyme Q reductase deficiencyC Antozzi, S Franceschetti, G Filippini, et al.Pageof 9