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In memoriam—Fernando José Carrera Carbó (1944–2024)
doi : 10.1093/ndt/gfae246
Volume 40, Issue 5, May 2025
Beyond ChatGPT: next generation artificial intelligence tools for nephrologists
doi : 10.1093/ndt/gfae223
Enhancing collaboration between academia and industry in kidney disease research Open Access
doi : 10.1093/ndt/gfae272
Acquired and genetic determinants of disease phenotype and therapeutic strategies in C3 glomerulopathy and immunoglobulin-associated MPGN
doi : 10.1093/ndt/gfae245
Exploring the metaverse: opportunities for nephrology in patient care and education
doi : 10.1093/ndt/gfae281
Tailored management strategies for IgA nephropathy based on clinical presentations Free
doi : 10.1093/ndt/gfae289
Effect of pharmacist interventions in chronic kidney disease: a meta-analysis Open Access
doi : 10.1093/ndt/gfae221
Cardiac magnetic resonance assessment of cardiac function across chronic kidney disease stages
doi : 10.1093/ndt/gfae222
Stenosis of the glomerulotubular neck in progressive chronic kidney disease
doi : 10.1093/ndt/gfae234
NINJ1-mediated macrophage plasma membrane rupture and neutrophil extracellular trap formation contribute to oxalate nephropathy
doi : 10.1093/ndt/gfae226
Hyperkalemia and maintenance of renin–angiotensin system inhibitor therapy after initiating SGLT-2 or DPP-4 inhibitors Open Access
doi : 10.1093/ndt/gfae227
Recovery from rituximab-associated persistent hypogammaglobulinaemia in children with nephrotic syndrome
doi : 10.1093/ndt/gfae228
Obinutuzumab versus rituximab for the treatment of refractory primary membranous nephropathy
doi : 10.1093/ndt/gfae230
Reference values for handgrip strength, five times sit-to-stand and gait speed in patients on hemodialysis
doi : 10.1093/ndt/gfae232
Epigenetic associations with kidney disease in individuals of African ancestry with APOL1 high-risk genotypes and HIV Open Access
doi : 10.1093/ndt/gfae237
Association of perinatal exposition to xenobiotics with kidney volume at birth
doi : 10.1093/ndt/gfae238
Inherited kidney disease and CAKUT are common causes of kidney failure requiring kidney replacement therapy: an ERA Registry study Open Access
doi : 10.1093/ndt/gfae240
Nephrectomy in autosomal dominant polycystic kidney disease: a consensus statement of the ERA Genes & Kidney Working Group Open Access
doi : 10.1093/ndt/gfaf019
Real-time monitoring of postfilter calcium in regional citrate anticoagulation for continuous renal replacement therapy
doi : 10.1093/ndt/gfaf006
The use of lung ultrasound monitoring and the risk of intradialysis hypotension in hemodialysis patients: an analysis in the context of a randomized clinical trial
doi : 10.1093/ndt/gfaf015
