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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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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
Xiaojun Li,Meijing Li,Rongkuan Li et al. Xiaojun Li et al.
Introduction: Managing active lupus nephritis (LN) in the presence of latent tuberculosis (TB) presents a significant treatment challenge. Traditional treatment with glucocorticoids combined with mycophenolic acid carries...
Olivia C Silveri,Feras Ghosheh Olivia C Silveri
Autosomal dominant polycystic kidney disease (ADPKD) is present in individuals with chronic renal disease due to bilateral renal cysts. This case report describes the progression of the disease with the rare complication of renal torsion of...
Maria Ilaria Moretti,Marta Leporati,Roberta Mazzucchelli et al. Maria Ilaria Moretti et al.
Introduction: Primary hyperoxaluria type 1 (PH1) is an inherited disease due to deficient activity of the liver enzyme AGT due to a mutation of the AGXT gene, leading to impairment in the glyoxylate metabolism with excess...
Tanja Kersnik Levart,Nina Olas Kar,Chiara Močnik Pegan et al. Tanja Kersnik Levart et al.
Introduction: Onasemnogene abeparvovec is one of the three disease-modifying therapies available that can significantly improve the outcome of patients with 5q-spinal muscular atrophy. Therapy-induced thrombotic microangi...
Abel Zemenfes Tsighe,Helen Gebremedhin Gebreegziabhier,Shephali Sharma Abel Zemenfes Tsighe
Introduction: Fibronectin glomerulopathy is a rare autosomal dominant disorder characterized by abnormal deposition of fibronectin within the kidney. It is associated with several variant mutations in the FN1 gene. It is ...
Malte Krakow,Johanna H Hinrichs,Judit Horvath et al. Malte Krakow et al.
Introduction: Atypical hemolytic uremic syndrome (aHUS), commonly considered the prototypical form of complement-mediated thrombotic microangiopathy, is caused by dysregulated complement activation, often triggered by gen...
Putu Angga Risky Raharja,I Putu Gde Fredy Gunawan,Gerhard Reinaldi Situmorang et al. Putu Angga Risky Raharja et al.
Introduction: Peritoneal dialysis (PD) has been demonstrated to be advantageous in the treatment of patients with end-stage kidney disease (ESKD), especially in children. However, patients undergoing PD may experience mec...
Melita Virpšaitė,Giedrė Žulpaitė,Marius Miglinas Melita Virpšaitė
Introduction: Purtscher-like retinopathy (PLR) is a rare retinal vasculopathy characterized by acute vision loss. It is typically associated with systemic diseases such as renal impairment. The combined incidence of Purts...
Azusa Kobayashi,Asami Takeda,Shoji Saito et al. Azusa Kobayashi et al.
Introduction: Complement 3 glomerulonephritis (C3GN) has a high recurrence rate after kidney transplantation. Before the disease became well understood, kidney transplantation was performed without a diagnosis of C3GN. Th...
Juan Pablo Gómez-Villarreal,Paola Borbolla-Flores,Ricardo Abraham Garza-Treviño et al. Juan Pablo Gómez-Villarreal et al.
Introduction: Untreated severe renal disease can be fatal, and renal replacement therapy (RRT) is often essential for survival. However, access to RRT can be limited by resource constraints, particularly in emergency or a...