Results 81 to 90 of about 60,277 (228)
DiagnosticsIntroduction: Focal segmental glomerulosclerosis (FSGS) is a pattern of kidney injury with diverse causes and pathogeneses, resulting in podocyte injury and depletion. It can be classified as primary, genetic, or secondary. Because FSGS classically has a
Gabriel Figueiredo +4 more
doaj +1 more source
HDL function and composition in atherothrombotic cardiovascular disease with very high HDL‐C
European Journal of Clinical Investigation, Volume 56, Issue 1, January 2026.We investigated 49 individuals (mean age: 62 ± 2 years, 83% female) with very high HDL‐C (>80 mg/dL), including 23 with ASCVD. Despite matched HDL‐C levels, functional and compositional HDL features differed between groups. CEC differences became evident only after tertile stratification, with ASCVD participants overrepresented in the lowest tertile ...
Teresa Padro +8 more
wiley +1 more source
Nephrotic syndrome in children during the COVID-19 pandemic
, 2022 Maniar Aesha +5 more
openalex +1 more source
Recent Progress in Double Filtration Plasmapheresis
Hemodialysis International, Volume 30, Issue 1, Page 18-25, January 2026.ABSTRACT Double‐filtration plasmapheresis is an advanced extracorporeal blood purification technique that selectively removes pathogenic macromolecules based on molecular weight. Unlike conventional plasma exchange, double‐filtration plasmapheresis uses a two‐step filtration process to retain beneficial plasma components such as albumin, while ...
Dan Li +3 more
wiley +1 more source
An Unusual Occurrence of Erythrocytosis in a Child with Nephrotic Syndrome and Advanced Chronic Kidney Disease [PDF]
, 2021 Ratna Acharya, Kiran Upadhyay
openalex +1 more source
First LDLRAP1 and Recurrent LDLR Mutations in Tunisian Families With Familial Hypercholesterolemia
Journal of Cellular and Molecular Medicine, Volume 30, Issue 1, January 2026.ABSTRACT Familial hypercholesterolemia (FH) is a genetic disorder characterised by elevated plasma LDL‐cholesterol, predisposing to premature atherosclerotic cardiovascular disease. Most cases follow an autosomal dominant pattern (ADH) caused by pathogenic variants in LDLR, APOB or PCSK9.
Wirath Ben Ncir +9 more
wiley +1 more source
Pediatric Transplantation, Volume 30, Issue 1, January 2026.AB0‐incompatible kidney transplantation in children can be performed with excellent results. Midterm outcome of AB0 incompatible KTx was not inferior to that of AB0 compatible KTx. Graft survival and graft function were comparably good in both groups. There was no increase in infectious complications or malignancies with AB0i KTx.
Christina Taylan +4 more
wiley +1 more source
High Steroid Sensitivity among Children with Nephrotic Syndrome in Southwestern Nigeria
International Journal of Nephrology, 2014 Recent reports from both Caucasian and black populations suggest changes in steroid responsiveness of childhood nephrotic syndrome. This study was therefore undertaken to determine the features and steroid sensitivity pattern of a cohort of black ...
Taiwo Augustina Ladapo +2 more
doaj +1 more source