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MRI Findings in Encephalopathy with Primary Carnitine Deficiency: A Case Report

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dc.contributor.authorYILMAZ, TEMEL FATİH
dc.contributor.authorATAY, Musa
dc.contributor.authorToprak, HÜSEYİN
dc.contributor.authorGULER, Serhat
dc.contributor.authorAralasmak, AYŞE
dc.contributor.authorAlkan, ALPAY
dc.contributor.institutionauthorYILMAZ, TEMEL FATİH
dc.contributor.institutionauthorTOPRAK, HÜSEYİN
dc.contributor.institutionauthorARALAŞMAK, AYŞE
dc.contributor.institutionauthorALKAN, ALPAY
dc.date.accessioned2019-10-05T21:30:39Z
dc.date.available2019-10-05T21:30:39Z
dc.date.issued2015-03-01
dc.description.abstractBACKGROUND AND PURPOSEWe presented MRI and DWI findings of a 12-year-old boy with primary carnitine deficiency, manifested with hypoglycemic hypoketotic encephalopathy.
dc.identifier10.1038/s41417-018-0017-2
dc.identifier.citationYILMAZ T. F. , ATAY M., Toprak H., GULER S., Aralasmak A., Alkan A., -MRI Findings in Encephalopathy with Primary Carnitine Deficiency: A Case Report-, JOURNAL OF NEUROIMAGING, cilt.25, ss.325-328, 2015
dc.identifier.pubmed24612242
dc.identifier.urihttps://hdl.handle.net/20.500.12645/7479
dc.language.isoen
dc.titleMRI Findings in Encephalopathy with Primary Carnitine Deficiency: A Case Report
dc.typeArticle
dspace.entity.typePublication
local.article.journalnameCancer gene therapy
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