MON-043 Characteristics, immunosuppression and progression in IgA nephropathy with hyperuricemia

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Modulating the progression in IgA nephropathy.

IgA nephropathy affects almost 1% of the population and yet the diagnosis is often missed. This significant kidney disease is often progressive with 25% of the patients going on to end-stage kidney disease over the course of 25 years. This minireview describes the clinical presentations in children and young adults. Therapeutic options are discussed including angiotensin-converting enzyme block...

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Intensive Supportive Care plus Immunosuppression in IgA Nephropathy.

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Uncoupling of Glomerular IgA Deposition and Disease Progression in Alymphoplasia Mice with IgA Nephropathy

Previous clinical and experimental studies have indicated that cells responsible for IgA nephropathy (IgAN), at least in part, are localized in bone marrow (BM). Indeed, we have demonstrated that murine IgAN can be experimentally reconstituted by bone marrow transplantation (BMT) from IgAN prone mice in not only normal mice, but also in alymphoplasia mice (aly/aly) independent of IgA+ cells hom...

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Predicting Progression of IgA Nephropathy: New Clinical Progression Risk Score

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High Prevalence of Hyperuricemia and Gout inNorth American Patients with IgA Nephropathy

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ژورنال

عنوان ژورنال: Kidney International Reports

سال: 2019

ISSN: 2468-0249

DOI: 10.1016/j.ekir.2019.05.830