2015
DOI: 10.1016/j.clineuro.2015.07.013
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A study of MRI changes in Wilson disease and its correlation with clinical features and outcome

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Cited by 28 publications
(27 citation statements)
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“…Additionally, reduction of the Vic in the putamen of WD patients was more prominent than other regions, which may reflect that the putamen is the most severely involved nucleus. The Vic and ODI showed no statistical difference between the right and left BG and thalamus, which indicates that disease onset in WD is bilaterally symmetrical, and these findings are consistent with previous reports …”
Section: Discussionsupporting
confidence: 92%
“…Additionally, reduction of the Vic in the putamen of WD patients was more prominent than other regions, which may reflect that the putamen is the most severely involved nucleus. The Vic and ODI showed no statistical difference between the right and left BG and thalamus, which indicates that disease onset in WD is bilaterally symmetrical, and these findings are consistent with previous reports …”
Section: Discussionsupporting
confidence: 92%
“…Conventional MR imaging did not reveal any signal changes in PSP, multisystem atrophy, and PD; whereas in WD, midbrain involvement occurred in 32.4%-49% of patients. 4,8,23 The involvement of the pons, cerebellum, and cerebellar peduncles, however, is rare in WD. The signal changes in the midbrain and pons in our patients, however, were not related to the midbrain and pons areas, respectively.…”
Section: Discussionmentioning
confidence: 99%
“…[3][4][5] The characteristic cranial MR imaging abnormalities in WD are corpus striatal involvement and the "giant Panda sign," which are reported in 14.3%-71.5% of patients. [6][7][8] Involvement of the pons and midbrain may lead to an abnormal postural reflex in WD, which may increase the neurologic disability. Recently, the MR Parkinsonism index (MRPI) has been reported to correctly differentiate progressive supranuclear palsy (PSP) from Parkinson disease (PD) and multisystem atrophy.…”
mentioning
confidence: 99%
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“…Bu genetik defekt sonrası safranın ekskresyonu azalır ve bakır karaciğer, böbrek, kornea, beyin ve diğer organlarda birikir. Nörolojik bulgular genellikle ikinci dekatta belirginleşir (2)(3)(4). Prognoz genellikle karaciğer tutulumunun şiddetine ve nörolojik tutuluma bağlıdır.…”
Section: Introductionunclassified