Nephrotic syndrome is a common renal disorder. In developed countries, the incidence is
reported to be 20 to 40 per million population while in the Indian subcontinent it is estimated …

Introduction Complement immunodeficiencies (excluding hereditary angioedema and
mannose binding lectin deficiency) are rare. Published literature consists largely of case …

Background: A revision of the International Society of Nephrology/Renal Pathology Society
(ISN/RPS) classification for lupus nephritis has been published in 2018. The current study …

Monoclonal gammopathy of undetermined significance (MGUS) is characterized by an M
spike less than 3 g/dL and a bone marrow containing fewer than 10% plasma cells and no …

Background Membranoproliferative glomerulonephritis (MPGN) is an uncommon glomerular
disorder that may lead to end stage renal disease (ESRD). With new understanding of the …

Genetic defects in complement regulatory proteins can lead to severe renal diseases,
including atypical hemolytic uremic syndrome and C3 glomerulopathies, and age-related …

Mass spectrometry based proteomics in the diagnosis of kidne... : Current Opinion in Nephrology
and Hypertension Mass spectrometry based proteomics in the diagnosis of kidney disease …

Historically, complement disorders have been attributed to immunodeficiency associated
with severe or frequent infection. More recently, however, complement has been recognized …

Background Eculizumab may be used to treat C3-glomerulopathy (C3G), a rare but severe
glomerular disease. Diagnosis and Treatment Patients 1, 2 and 3 were diagnosed with …

Glomerulopathies are one of the leading causes of end-stage renal disease. In the last
years, clinical research has made significant contributions to the understanding of such …