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dc.contributor.authorYildiz, Melek
dc.contributor.authorMagen, Daniella
dc.contributor.authorOfir, Ayala
dc.contributor.authorTzur, Shay
dc.contributor.authorHassan, Nisreen
dc.contributor.authorGoldman, Michael
dc.contributor.authorDemir, Korcan
dc.contributor.authorBahat, Hilla
dc.date.accessioned2021-03-05T16:26:52Z
dc.date.available2021-03-05T16:26:52Z
dc.date.issued2017
dc.identifier.citationDemir K., Yildiz M., Bahat H., Goldman M., Hassan N., Tzur S., Ofir A., Magen D., "Clinical Heterogeneity and Phenotypic Expansion of NaPi-IIa-Associated Disease", JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, cilt.102, ss.4604-4614, 2017
dc.identifier.issn0021-972X
dc.identifier.otherav_c0abeb51-e2ac-4667-9aab-33940954b286
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/127892
dc.identifier.urihttps://doi.org/10.1210/jc.2017-01592
dc.description.abstractContext: NaPi-IIa, encoded by SLC34A1, is a key phosphate transporter in the mammalian proximal tubule and plays a cardinal role in renal phosphate handling. NaPi-IIa impairment has been linked to various overlapping clinical syndromes, including hypophosphatemic nephrolithiasis with osteoporosis, renal Fanconi syndrome with chronic kidney disease, and, most recently, idiopathic infantile hypercalcemia and nephrocalcinosis.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectENDOKRİNOLOJİ VE METABOLİZMA
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectEndokrinoloji ve Metabolizma Hastalıkları
dc.titleClinical Heterogeneity and Phenotypic Expansion of NaPi-IIa-Associated Disease
dc.typeMakale
dc.relation.journalJOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
dc.contributor.departmentDokuz Eylül Üniversitesi , ,
dc.identifier.volume102
dc.identifier.issue12
dc.identifier.startpage4604
dc.identifier.endpage4614
dc.contributor.firstauthorID2273951


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