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Infantile sandhoff s disease multivoxel magnetic resonance spectroscopy findings

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dc.contributor.author Alkan, Alpay
dc.contributor.author Kutlu, Ramazan
dc.contributor.author Yakıncı, Mehmet Cengiz
dc.contributor.author Sığırcı, Ahmet
dc.contributor.author Aslan, Mehmet
dc.contributor.author Saraç, Kaya
dc.date.accessioned 2017-06-24T11:33:30Z
dc.date.available 2017-06-24T11:33:30Z
dc.date.issued 2003
dc.identifier.citation Alkan, A. Kutlu, R. Yakıncı, M. C. Sığırcı, A. Aslan, M. Saraç, K. (2003). Infantile sandhoff s disease multivoxel magnetic resonance spectroscopy findings. J Child Neurol. 18:425–428. tr_TR
dc.identifier.uri http://hdl.handle.net/11616/7185
dc.description.abstract Sandhoff’s disease is a rare, genetic lysosomal storage disease leading to delayed myelination or demyelination. Although neuroimaging findings in this disease have been reported previously, magnetic resonance spectroscopy findings have not been reported. In this report, we present magnetic resonance imaging and magnetic resonance spectroscopy features of two cases with Sandhoff’s disease. Magnetic resonance spectroscopy revealed findings indicating widespread demyelination in both cases and neuroaxonal loss and anaerobic metabolism in the second case. Magnetic resonance spectroscopy could provide useful information in the explanation of the clinical picture of cases with Sandhoff’s disease. tr_TR
dc.language.iso eng tr_TR
dc.publisher J Child Neurol tr_TR
dc.rights info:eu-repo/semantics/openAccess tr_TR
dc.title Infantile sandhoff s disease multivoxel magnetic resonance spectroscopy findings tr_TR
dc.type article tr_TR
dc.relation.journal J Child Neurol tr_TR
dc.contributor.department İnönü Üniversitesi tr_TR
dc.contributor.authorID 7768 tr_TR
dc.identifier.volume 18 tr_TR
dc.identifier.startpage 425 tr_TR
dc.identifier.endpage 428 tr_TR

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