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Giant axonal neuropathy MRS findings

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dc.contributor.author Alkan, Alpay
dc.contributor.author Kutlu, Ramazan
dc.contributor.author Sığırcı, Ahmet
dc.contributor.author Baysal, Tamer
dc.contributor.author Altınok, Tayfun
dc.contributor.author Yakıncı, Mehmet Cengiz
dc.date.accessioned 2017-06-24T07:10:09Z
dc.date.available 2017-06-24T07:10:09Z
dc.date.issued 2003
dc.identifier.citation Alkan, A. Kutlu, R. Sığırcı, A. Baysal, T. Altınok, T. Yakıncı, M. C. (2003). Giant Axonal Neuropathy MRS Findings. J Neuroimaging, (13), 371–375. tr_TR
dc.identifier.uri http://hdl.handle.net/11616/7175
dc.description.abstract Giant axonal neuropathy (GAN) is a rare genetic disease of childhood involving the central and peripheral nervous systems. Axonal loss with several giant axons filled with neurofilaments is the main histopathological feature of peripheral nerve biopsies in this disease. Routine neuroimaging studies reveal diffuse hyperintensities in cerebral and cerebellar white matter. In this case report,the authors present the brain magnetic resonance spectroscopic features (normal N-acetylaspartate/ creatine and increased choline/creatine and myoinositol/creatine ratios),which might indicate the absence of neuroaxonal loss and the presence of significant demyelination and glial proliferation in white matter, of an 11-year-old boy diagnosed with GAN. tr_TR
dc.language.iso eng tr_TR
dc.publisher J Neuroimaging tr_TR
dc.rights info:eu-repo/semantics/openAccess tr_TR
dc.subject Giant axonal neuropathy tr_TR
dc.subject Magnetic resonance spectroscopy tr_TR
dc.title Giant axonal neuropathy MRS findings tr_TR
dc.type article tr_TR
dc.relation.journal J Neuroimaging tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.contributor.authorID 7768 tr_TR
dc.identifier.volume 13 tr_TR
dc.identifier.startpage 371 tr_TR
dc.identifier.endpage 375 tr_TR


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