作者
Felicitas E. Hengel,Silke Dehde,Moritz Lassé,Gunther Zahner,Larissa Seifert,Annabel Schnarre,Oliver Kretz,Fatih Demir,Hans O Pinnschmidt,Florian Grahammer,Renke Lucas,Lea Maxima Mehner,Tom Zimmermann,A. Billing,Jun Oh,Adele Mitrotti,Paola Pontrelli,Hanna Dębiec,Claire Dossier,Manuela Colucci,Francesco Emma,William E Smoyer,Astrid Weins,Franz Schaefer,Nada Alachkar,Anke Diemert,Julien Hogan,Elion Hoxha,Thorsten Wiech,Markus M Rinschen,Pierre Ronco,Marina Vivarelli,Loreto Gesualdo,Nicola M Tomas,Tobias B. Huber
摘要
Minimal change disease and primary focal segmental glomerulosclerosis in adults, along with idiopathic nephrotic syndrome in children, are immune-mediated podocytopathies that lead to nephrotic syndrome. Autoantibodies targeting nephrin have been found in patients with minimal change disease, but their clinical and pathophysiological roles are unclear.