Lodi R.; Kemp G.J.; Muntoni F.; Thompson C.H.; Rae C.; Taylor J.; Styles P.; Taylor D.J., Reduced cytosolic acidification during exercise suggests defective glycolytic activity in skeletal muscle of patients with Becker muscular dystrophy. An in vivo 31P magnetic resonance spectroscopy study, «BRAIN», 1999, 122, pp. 121 - 130 [articolo]
Russell J.M Lane; Michael C Barrett; Doris J Taylor; Graham J Kemp; Raffaele Lodi, Heterogeneity in chronic fatigue syndrome: evidence from magnetic resonance spectroscopy of muscle, «NEUROMUSCULAR DISORDERS», 1998, 8, pp. 204 - 209 [articolo]
Lodi R.; Taylor D.J.; Tabrizi S.J.; Hilton-Jones D.; Squier M.V.; Seller A.; Styles P.; Schapira A.H.V., Normal in vivo skeletal muscle oxidative metabolism in sporadic inclusion body myositis assessed by 31P-magnetic resonance spectroscopy, «BRAIN», 1998, 121, pp. 2119 - 2126 [articolo]
Lodi R.; Taylor D.J.; Radda G.K.; McCully K., Chronic fatigue syndrome and skeletal muscle mitochondrial function (multiple letters), «MUSCLE & NERVE», 1997, 20, pp. 765 - 766 [articolo]
Lodi R.; Muntoni F.; Taylor J.; Kumar S.; Sewry C.A.; Blamire A.; Styles P.; Taylor D.J., Correlative MR imaging and 31P-MR spectroscopy study in sarcoglycan deficient limb girdle muscular dystrophy, «NEUROMUSCULAR DISORDERS», 1997, 7, pp. 505 - 511 [articolo]
Lodi R.; Taylor D.J.; Tabrizi S.J.; Kumar S.; Sweeney M.; Wood N.W.; Styles P.; Radda G.K.; Schapira A.H.V., In vivo skeletal muscle mitochondrial function in Leber's hereditary optic neuropathy assessed by 31P magnetic resonance spectroscopy, «ANNALS OF NEUROLOGY», 1997, 42, pp. 573 - 579 [articolo]
Fabrizi G.M.; Lodi R.; D'Ettorre M.; Malandrini A.; Cavallaro T.; Rimoldi M.; Zaniol P.; Barbiroli B.; Guazzi G., Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy a pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defect, «JOURNAL OF THE NEUROLOGICAL SCIENCES», 1996, 137, pp. 20 - 27 [articolo]
Massa R.; Lodi R.; Barbiroli B.; Servidei S.; Sancesario G.; Manfredi G.; Zaniol P.; Bernardi G., Partial block of glycolysis in late-onset phosphofructokinase deficiency myopathy, «ACTA NEUROPATHOLOGICA», 1996, 91, pp. 322 - 329 [articolo]
Uncini A.; Lodi R.; Di Muzio A.; Silvestri G.; Servidei S.; Lugaresi A.; Iotti S.; Zaniol P.; Barbiroli B., Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine, «JOURNAL OF THE NEUROLOGICAL SCIENCES», 1995, 129, pp. 214 - 222 [articolo]
Uncini A.; Lodi R.; Di Muzio A.; Silvestri G.; Servidei S.; Lugaresi A.; Iotti S.; Zaniol P.; Barbiroli B., Abnormal brain and muscle energy metabolism shown by 31P-MRS in familial hemiplegic migraine, «JOURNAL OF THE NEUROLOGICAL SCIENCES», 1995, 129, pp. 214 - 222 [articolo]
Antozzi C.; Franceschetti S.; Filippini G.; Barbiroli B.; Savoiardo M.; Fiacchino F.; Rimoldi M.; Lodi R.; Zaniol P.; Zeviani M., Epilepsia partialis continua associated with NADH-coenzyme Q reductase deficiency, «JOURNAL OF THE NEUROLOGICAL SCIENCES», 1995, 129, pp. 152 - 161 [articolo]
Sacquegna T.; Lodi R.; De Carolis P.; Tinuper P.; Cortelli P.; Zaniol P.; Funicello R.; Montagna P.; Barbiroli B., Brain energy metabolism studied by 31P‐MR spectroscopy in a case of migraine with prolonged aura, «ACTA NEUROLOGICA SCANDINAVICA», 1992, 86, pp. 376 - 380 [articolo]
