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dc.contributor.authorKarch, André
dc.contributor.authorManthey, Henrike
dc.contributor.authorPonto, Claudia
dc.contributor.authorHermann, Peter
dc.contributor.authorHeinemann, Uta
dc.contributor.authorSchmidt, Christian
dc.contributor.authorZerr, Inga
dc.date.accessioned2014-01-21T13:24:20Z
dc.date.available2014-01-21T13:24:20Z
dc.date.issued2013
dc.identifier.citationInvestigating the Association of ApoE Genotypes with Blood-Brain Barrier Dysfunction Measured by Cerebrospinal Fluid-Serum Albumin Ratio in a Cohort of Patients with Different Types of Dementia. 2013, 8 (12):e84405 PLoS ONEen
dc.identifier.issn1932-6203
dc.identifier.pmid24386372
dc.identifier.doi10.1371/journal.pone.0084405
dc.identifier.urihttp://hdl.handle.net/10033/311617
dc.description.abstractSince more than a decade ApoE is known to be a strong risk factor for Alzheimer's disease (AD); however, molecular pathways mediating this risk are still unclear. In recent years it has been hypothesized that ApoE might play a role in the disintegration of blood-brain barrier (BBB). In the present study we addressed the question if ApoE genotypes might be associated with BBB function measured by albumin ratio (QAlb) in a large cohort of patients with different types of dementia.
dc.language.isoenen
dc.rightsArchived with thanks to PloS oneen
dc.titleInvestigating the Association of ApoE Genotypes with Blood-Brain Barrier Dysfunction Measured by Cerebrospinal Fluid-Serum Albumin Ratio in a Cohort of Patients with Different Types of Dementia.en
dc.typeArticleen
dc.identifier.journalPloS oneen
refterms.dateFOA2018-06-12T18:12:24Z
html.description.abstractSince more than a decade ApoE is known to be a strong risk factor for Alzheimer's disease (AD); however, molecular pathways mediating this risk are still unclear. In recent years it has been hypothesized that ApoE might play a role in the disintegration of blood-brain barrier (BBB). In the present study we addressed the question if ApoE genotypes might be associated with BBB function measured by albumin ratio (QAlb) in a large cohort of patients with different types of dementia.


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