1996
DOI: 10.1016/0730-725x(95)02053-v
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Disappearance of multiple sclerosis lesions with severely prolonged T1 on images obtained by a flair pulse sequence

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Cited by 11 publications
(3 citation statements)
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“…It is not surprising, therefore, that in the current study, the volume of posterior fossa lesions is greater in CSE and the volume of subcortical lesions is greater in fFLAIR (table 4). It has been reported that heavily T1 weighted lesions in the periventricular regions may disappear on FLAIR images36 and in this context it is notable that we found no significant difference in periventricular lesion volumes. This may be because such high T1 lesions are embedded in high signal areas on fFLAIR images and are therefore measured.…”
Section: Discussionsupporting
confidence: 61%
“…It is not surprising, therefore, that in the current study, the volume of posterior fossa lesions is greater in CSE and the volume of subcortical lesions is greater in fFLAIR (table 4). It has been reported that heavily T1 weighted lesions in the periventricular regions may disappear on FLAIR images36 and in this context it is notable that we found no significant difference in periventricular lesion volumes. This may be because such high T1 lesions are embedded in high signal areas on fFLAIR images and are therefore measured.…”
Section: Discussionsupporting
confidence: 61%
“…The same may occur with multiple sclerosis lesions severely hypointense on T1-WI. 42 MRI-pathological correlation studies performed to determine the background of age-related subcortical gray and white matter hyperintensities on T2-WI found different types of pathology: infarctions, gliosis, myelin and axonal loss, breakdown of the ependymal lining, and enlarged perivascular spaces. 17,[43][44][45][46][47] Areas of myelin pallor can be hyperintense on T2-WI but isointense on T1-WI, 17,45 and it seems possible that differences in type of pathology can also influence detection on FLAIR.…”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, the FLAIR sequence, which provides T 2 ‐weighted images with attenuated cerebrospinal fluid (CSF) signals, has shown promising results due to its high contrast resolution and decrease in the number of artifacts close to CSF. Although the advantages of the FLAIR sequence over the T 2 ‐weighted sequence have been reported by several authors (1–7), some reports have indicated the disadvantages of the FLAIR sequence (8–10). Currently, the FLAIR sequence is generally used in combination with the T 2 ‐weighted sequence to provide additional information.…”
mentioning
confidence: 99%