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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.Neurology|April 1, 1994
31P-magnetic resonance spectroscopy in migraine without auraP Montagna, P Cortelli, L Monari, 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.Journal of the Neurological Sciences|April 1, 1995
Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraineA Uncini, R Lodi, A Di Muzio, et al.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.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.Journal of the Neurological Sciences|August 1, 1991
Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patientN Bresolin, P Martinelli, B Barbiroli, et al.Journal of Neurology|March 1, 1995
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and CA Toscano, M C Fazio, G Vita, et al.Pageof 5