期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (8)
Introduction: Secondary steroid-resistant nephrotic syndrome (SRNS) refers to the condition when patients with initial steroid-sensitive nephrotic syn......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (8)
Introduction: WT1 missense mutation in exon 8 or 9 causes infantile nephrotic syndrome with early progression to end-stage kidney disease (ESKD), Wilm......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (3)
Introduction: Stress related disorders (SRDs, i.e., psychiatric disorders induced by significant life stressors) increase vulnerability to health prob......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (4)
Introduction: Caregivers are essential for the health, safety, and independence of many patients and incur financial and personal cost in this role, i......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (2)
Introduction: Most of the approximately 60 genes that if mutated cause steroid-resistant nephrotic syndrome (SRNS) are highly expressed in the glomeru......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (2)
Introduction: Steroid-resistant nephrotic syndrome (SRNS) is the second most common cause of chronic kidney disease during childhood. Identification o......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (2)
Introduction: Immunoglobulin A nephrology (IgAN), characterized by co-deposition of IgA and complement components, is an activation of complement syst......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (2)
Introduction: Hypokalemia, including normal range values <4 mEq/l, has been associated with increased peritonitis and mortality in patients with pe......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (3)
Introduction: Roxadustat is an oral hypoxia-inducible factor prolyl hydroxylase inhibitor that stimulates erythropoiesis and improves iron metabolism.......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (1)
Introduction: Kidney and liver cysts in autosomal dominant polycystic kidney disease (ADPKD) can compress the inferior vena cava (IVC), but IVC compre......
期刊： KIDNEY INTERNATIONAL REPORTS, 2021; 6 (1)
Introduction: Familial IgA nephropathy (IgAN) has been widely reported. However, its clinicohistologic characteristics and long-term prognosis are not......
