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dc.contributor.authorManara, Renzo-
dc.contributor.authorRizzo, Mónica del-
dc.contributor.authorBurlina, A. P.-
dc.contributor.authorBordugo, A.-
dc.contributor.authorCitton, V.-
dc.contributor.authorRodríguez-Pombo, Pilar-
dc.contributor.authorUgarte, Magdalena-
dc.contributor.authorBurlina, A. B.-
dc.date.accessioned2015-05-19T11:05:14Z-
dc.date.available2015-05-19T11:05:14Z-
dc.date.issued2012-
dc.identifierissn: 0141-8955-
dc.identifier.citationJournal of Inherited Metabolic Disease 35: 413- 417 (2012)-
dc.identifier.urihttp://hdl.handle.net/10261/115405-
dc.description.abstractWe describe a new neuroradiologic picture observed during metabolic decompensation in two maple syrup urine disease (MSUD) patients that resemblesWernicke encephalopathy (WE). Clinical observations and the review of the literature regarding WE and MSUD pathophysiology prompted us to hypothesize a pathogenic link between these two disorders. Based on these findings, clinicians and neuroradiologists should be aware of MSUD as a possible predisposing factor of WE in children.-
dc.description.sponsorshipCentro Regionale Malattie Metaboliche Ereditarie; Associazione Studio Malattie Metaboliche Ereditarie-
dc.publisherKluwer Academic Publishers-
dc.rightsclosedAccess-
dc.titleWernicke-like encephalopathy during classic maple syrup urine disease decompensation-
dc.typeartículo-
dc.identifier.doi10.1007/s10545-012-9456-3-
dc.date.updated2015-05-19T11:05:14Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.contributor.funderCentro Regionale Malattie Metaboliche Ereditarie della Regione Veneto-
dc.contributor.funderAssociazione Studio Malattie Metaboliche Ereditarie-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeartículo-
item.grantfulltextnone-
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