1986
DOI: 10.1016/0730-725x(86)90903-3
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In - vivo proton spin lattice relaxation times in normal and dystrophic muscles

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(2 citation statements)
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“…Measurements of relaxation times have been used to discriminate muscle in patients with Duchenne muscular dystrophy from muscle in healthy controls. 11,18 To our knowledge, the same study has not been undertaken in the brain of patients with Duchenne dystrophy. The T2 values in muscle change with progression of the disease in humans, indicating that they can be used to follow both progression and therapy.…”
Section: Discussionmentioning
confidence: 99%
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“…Measurements of relaxation times have been used to discriminate muscle in patients with Duchenne muscular dystrophy from muscle in healthy controls. 11,18 To our knowledge, the same study has not been undertaken in the brain of patients with Duchenne dystrophy. The T2 values in muscle change with progression of the disease in humans, indicating that they can be used to follow both progression and therapy.…”
Section: Discussionmentioning
confidence: 99%
“…The T1 relaxation time has been shown to be significantly higher in dystrophic chicken muscle than in the control. 17,18 In patients with Duchenne muscular dystrophy, T1 is initially higher than controls and decreases to a value lower than controls. The elevated T1 in younger individuals has been attributed to higher water content 16 and the reduction with age correlates with increased muscle fat content.…”
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confidence: 99%