Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/5249
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dc.contributor.authorMahmoud, Talaen_US
dc.contributor.authorGhandour, Elias Cen_US
dc.contributor.authorJaar, Bernard Gen_US
dc.date.accessioned2021-12-15T08:53:31Z-
dc.date.available2021-12-15T08:53:31Z-
dc.date.issued2021-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/5249-
dc.description.abstractOxalate nephropathy is a rare disorder that can result in acute kidney injury (AKI) and progresses to end-stage kidney disease (ESKD). The causes can be either primary or secondary. Primary hyperoxaluria includes a group of hereditary disorders with enzymatic defects in the glyoxylate pathway, resulting in decreased oxalate metabolism. Secondary hyperoxaluria, often overlooked can result from increased intestinal absorption, nutritional deficiencies, decreased fluid intake, impaired excretion, and increased dietary consumption of oxalate.en_US
dc.language.isoengen_US
dc.publisherNational Library of Medicineen_US
dc.subjectAcute kidney injuryen_US
dc.subjectChronic kidney diseaseen_US
dc.subjectDieten_US
dc.subjectEnd-stage kidney diseaseen_US
dc.subjectHyperoxaluriaen_US
dc.subjectNephrolithiasisen_US
dc.subjectOxalateen_US
dc.subjectOxalosisen_US
dc.subjectVegetablesen_US
dc.titleA hidden cause of oxalate nephropathy: a case reporten_US
dc.typeJournal Articleen_US
dc.identifier.doi10.1186/s13256-021-02732-6-
dc.identifier.pmid33678172-
dc.identifier.scopus2-s2.0-85102115027-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85102115027-
dc.contributor.affiliationFaculty of Medicineen_US
dc.description.volume15en_US
dc.date.catalogued2021-12-15-
dc.description.statusPublisheden_US
dc.identifier.openURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7938566/en_US
dc.relation.ispartoftextJournal of Medical Case Reportsen_US
Appears in Collections:Faculty of Medicine
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