“…Examples of markers of disease using 31 P MRS can be found throughout the literature in which the levels of 31 P metabolites and/or their fluxes are modified due to specific illnesses. In vivo 31 P spectral alterations in acquired and genetic pathological human muscle conditions such as dermatomyositis and polymyositis [72], muscle dystrophies [73][74][75][76], ischemia [77], sporadic inclusion body myositis [78], progressive supranuclear palsy [79], malignant hyperthermia [80], fibromyalgia [81], pustular psoriasis [82], retinitis pigmentosa [83], Parkinson disease [84], McArdle's syndrome [85], adenylsuccinate lyase deficiency [86], hypo-ß-lipoproteinae mia [87], and some mitochondrial myopathies (cytochrome bc1 deficiency [88], carriers of 11778 mtD-NA mutation [89], NARP syndrome [90], phosphofructokinase deficiency [91,92], Leber disease [93][94][95], and piruvate dehydrogenase complex deficiency [96] have been reported. The usual change found using 31 P MRS in these diseases is a reduction in the bioenergetics of the tissue.…”