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期刊名:Case reports in nephrology and dialysis

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ISSN:2296-9705

e-ISSN:2296-9705

IF/分区:0.9/Q4

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共收录本刊相关文章索引342
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Ciaran Twomey Brenner,Sujit Saha,Kate Bramham et al. Ciaran Twomey Brenner et al.
Introduction: Anti-glomerular basement membrane (GBM) disease is a rare cause of glomerulonephritis usually mediated by IgG antibodies and is associated with ANCA-associated glomerulonephritis in up to 50% of cases. IgA-m...
Neva Bezeljak,Alexander Jerman,Damjan Grenc et al. Neva Bezeljak et al.
Introduction: Salbutamol is a moderately selective beta-2-adrenergic agonist. Various side effects can occur because of beta-1 and beta-2 receptor activation. Due to the large volume of distribution, it is not considered ...
Javier Burgos Martín,Marina Almenara Tejederas,Fabiola Alonso García et al. Javier Burgos Martín et al.
Introduction: Xanthogranulomatous pyelonephritis (XGP) is a rare illness that consists of a destructive chronic inflammatory process of the renal parenchyma associated with recurrent infection and obstructions of the urin...
Elizabet Artinyan,Nikolay Dimov,Marina Vaysilova Elizabet Artinyan
Introduction: Emphysematous pyelonephritis is a rare but potentially life-threatening urinary tract infection characterized by the formation of gas in the renal parenchyma, collecting system, and perinephric tissue. The c...
Tomáš Seeman,Terezie Šuláková,Alice Bosáková et al. Tomáš Seeman et al.
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, which is mainly caused by pathogenic variants in two particular genes: PKD1 and PKD2. ADPKD caused by varian...
Simeon Schietzel,Sarah Jane Rippin Wagner,Luzia Nigg Calanca Simeon Schietzel
Introduction: Acute pancreatitis is an infrequent but challenging cause of peritonitis in peritoneal dialysis (PD). Presentation is often indistinguishable from infectious peritonitis, interpretation of pancreatic enzymes...
Liliana Italia De Rosa,Martina Catania,Francesca Tunesi et al. Liliana Italia De Rosa et al.
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic kidney disease and the 4th leading cause of renal replacement therapy in the world. ADPKD is a systemic disorder as cysts may d...
Sawako Yoshida,Eriko Tanaka,Zentaro Kiuchi et al. Sawako Yoshida et al.
Introduction: Hemolytic uremic syndrome (HUS) is characterized by progressive kidney injury accompanied by thrombotic microangiopathy, which is clinically defined as microangiopathic hemolytic anemia with thrombocytopenia...
Yanqin Fan,Dejiao He,Jing Cheng et al. Yanqin Fan et al.
Introduction: Stuck tunneled central venous catheters (CVCs) have been increasingly reported. In rare cases, the impossibility of extracting the CVC from the central vein after regular traction is the result of rigid adhe...
Angela Maria Cordoba-Hurtado,Laura Fuentes-Mendez,Lucia Monserrat Perez-Navarro et al. Angela Maria Cordoba-Hurtado et al.
Introduction: The presence of three different entities in a single patient is usually of clinical interest and mostly anecdotal. The overlap of systemic sclerosis (SSc), Sjögren syndrome (SS), and ANCA-associated renal-l...