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Increased risk for kidney sequelae surrogates in survivors of Wilms tumor

dc.contributor.authorAPAK, HİLMİ
dc.contributor.authorCanpolat, Nur
dc.contributor.authorKonukoglu, Dildar
dc.contributor.authorCaliskan, Salim
dc.contributor.authorSever, Lale
dc.contributor.authorArslan, Emrullah
dc.contributor.authorSAYGILI, Seha Kamil
dc.contributor.authorCelkan, Tulin Tiraje
dc.contributor.authorKurugoglu, Sebuh
dc.contributor.authorElicevik, Mehmet
dc.contributor.authorCamcioglu, Abdulhamit Enes
dc.date.accessioned2022-02-18T09:13:30Z
dc.date.available2022-02-18T09:13:30Z
dc.identifier.citationArslan E., SAYGILI S. K. , Celkan T. T. , Kurugoglu S., Elicevik M., Camcioglu A. E. , Konukoglu D., APAK H., Caliskan S., Sever L., et al., "Increased risk for kidney sequelae surrogates in survivors of Wilms tumor", PEDIATRIC NEPHROLOGY, 2022
dc.identifier.issn0931-041X
dc.identifier.othervv_1032021
dc.identifier.otherav_2634c05c-3cfb-4b1e-ac70-6aea2c4f2f22
dc.identifier.urihttp://hdl.handle.net/20.500.12627/176779
dc.identifier.urihttps://doi.org/10.1007/s00467-022-05460-1
dc.description.abstractBackground There is evidence of increased risk of hypertension, albuminuria, and development of chronic kidney disease (CKD) in long-term follow-up of survivors of Wilms tumor (WT). However, most studies were conducted in heterogeneous groups, including patients with solitary kidney. In addition, little is known about tubular dysfunction. This study aimed to investigate kidney sequelae, including CKD development, hypertension, and glomerular and tubular damage in WT survivors.
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectİç Hastalıkları
dc.subjectNefroloji
dc.subjectPediatrics
dc.subjectNephrology
dc.subjectUrology
dc.subjectPediatrics, Perinatology and Child Health
dc.subjectHealth Sciences
dc.subjectTıp
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.titleIncreased risk for kidney sequelae surrogates in survivors of Wilms tumor
dc.typeMakale
dc.relation.journalPEDIATRIC NEPHROLOGY
dc.contributor.departmentİstanbul Teknik Üniversitesi , ,
dc.contributor.firstauthorID3390384


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