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dc.contributor.authorÜnal Uzun, Özlem
dc.contributor.authorCengiz, Nurcan
dc.contributor.authorÇavdarlı, Büşra
dc.contributor.authorBayrakçı, Umut
dc.contributor.authorKiremitçi, Saba
dc.contributor.authorKüçükçongar Yavaş, Aynur
dc.date.accessioned2021-02-05T08:09:28Z
dc.date.available2021-02-05T08:09:28Z
dc.date.issued2021en_US
dc.identifier.citationUzun, Ö.Ü., Cengiz, N., Çavdarlı, B. et al. Proteinuria and progressive kidney failure due to an inborn error of metabolism: Questions. Pediatr Nephrol (2021). https://doi.org/10.1007/s00467-020-04891-yen_US
dc.identifier.issn0931-041X
dc.identifier.issn1432-198X
dc.identifier.urihttps://hdl.handle.net/20.500.12809/8933
dc.identifier.urihttps://doi.org/10.1007/s00467-020-04891-y
dc.description.abstractA 6-year-old patient was admitted to our clinic with a suspected diagnosis of an inborn error of metabolism (IEM). He was born at term with a birth weight of 3620 g with an uneventful delivery. He was the first child of nonconsanguineous Turkish parents, and his sibling was healthy.en_US
dc.item-language.isoengen_US
dc.publisherSpringerLinken_US
dc.relation.isversionof10.1007/s00467-020-04891-yen_US
dc.item-rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectChilden_US
dc.subjectInborn error of metabolismen_US
dc.subjectAnemiaen_US
dc.subjectProteinuriaen_US
dc.subjectDysostosis multiplexen_US
dc.subjectKidney diseaseen_US
dc.subjectCherry-red spoten_US
dc.titleProteinuria and progressive kidney failure due to an inborn error of metabolism: Questionsen_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.contributor.authorID0000-0002-4977-8310en_US
dc.contributor.institutionauthorCengiz, Nurcan
dc.relation.journalPediatric Nephrologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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