dc.creatorEMBIRUCU, E. K.
dc.creatorOTADUY, M. C. G.
dc.creatorTANEJA, A. K.
dc.creatorLEITE, C. C.
dc.creatorKOK, F.
dc.creatorLUCATO, L. T.
dc.date.accessioned2012-10-19T17:01:32Z
dc.date.accessioned2018-07-04T15:04:28Z
dc.date.available2012-10-19T17:01:32Z
dc.date.available2018-07-04T15:04:28Z
dc.date.created2012-10-19T17:01:32Z
dc.date.issued2010
dc.identifierAMERICAN JOURNAL OF NEURORADIOLOGY, v.31, n.7, p.1347-1349, 2010
dc.identifier0195-6108
dc.identifierhttp://producao.usp.br/handle/BDPI/21449
dc.identifier10.3174/ajnr.A1885
dc.identifierhttp://dx.doi.org/10.3174/ajnr.A1885
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1618224
dc.description.abstractCTX is a rare lipid-storage disease. Novel MRS findings from 3 patients, using a short TE, were the presence of lipid peaks at 0.9 and 1.3 ppm in the depth of the cerebellar hemisphere; this might represent an additional marker of disease that is CNS-specific and noninvasive. A decrease in NAA concentration was also detected and attributed to neuroaxonal damage. One patient presented an increase in mlns concentration, pointing to gliosis and astrocytic proliferation.
dc.languageeng
dc.publisherAMER SOC NEURORADIOLOGY
dc.relationAmerican Journal of Neuroradiology
dc.rightsCopyright AMER SOC NEURORADIOLOGY
dc.rightsrestrictedAccess
dc.titleMR Spectroscopy Detects Lipid Peaks in Cerebrotendinous Xanthomatosis
dc.typeArtículos de revistas


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