Danilo Candido de Almeida,Juan Sebastian Henao Agudelo
Danilo Candido de Almeida
Irisin, a myokine generated through the proteolytic cleavage of fibronectin type III domain-containing protein 5 (FNDC5), has been increasingly recognized as a critical mediator of the salutary effects of physical exercise on metabolic home...
Kidney transplantation for the treatment of ESRD caused by hereditary type 2 Dent Nephropathy which carries a rare ORCL mutation [0.03%]
罕见的ORCL突变遗传性2型登特肾病所致终末期肾病的治疗与肾脏移植
Chuanyou Xia,Lingquan Meng,Guanbao Tang et al.
Chuanyou Xia et al.
María Carande Del Río,Nicolas R Robles,Alfonso Parejo Martín et al.
María Carande Del Río et al.
Introduction: The reference sample for quantifying alpha-1-microglobulin is 24-h urine. However, although it is usually quantified in the second urine sample of the morning, the first urine sample of the morning is the le...
Results of a national survey on the diagnosis of heart failure in nephrology clinics: a call to action [0.03%]
一项关于肾病门诊心力衰竭诊断的全国调查及其启示
Mariá Marques Vidas,Javier Diez,Patricia de Sequera et al.
Mariá Marques Vidas et al.
Introduction: Heart failure (HF) is a common comorbidity with a major prognostic impact in patients with chronic kidney disease (CKD). However, screening and diagnostic practices for HF in nephrology clinics are not optim...
Lecithin-cholesterol acyltransferase deficiency with the finding of "zebra bodies": A diagnostic challenge in the context of suspected Fabry disease [0.03%]
磷脂酰胆碱胆固醇酰基转移酶缺乏并出现“条纹体”：在疑似法布雷病背景下具有诊断挑战性的一个病例报告
Juan Enrique Rodriguez Mori,Milagros Del Pilar Dapello Jimenez,Julia Sumire Umeres et al.
Juan Enrique Rodriguez Mori et al.
Lecithin-cholesterol acyltransferase (LCAT) deficiency is a rare autosomal recessive disorder resulting from mutations in the LCAT gene, which leads to abnormal lipoprotein metabolism. This results in markedly reduced high-density lipoprote...
Case Reports
Nefrologia. 2026 Feb 19:501444. DOI:10.1016/j.nefroe.2026.501444 2026
Therapeutic Apheresis Registry of the Spanish Society of Nephrology. Analysis of activity over the last five years [0.03%]
西班牙肾病学会血浆置换治疗注册中心分析近五年报告
E Rodríguez,L Sánchez-Cámara,E Márquez et al.
E Rodríguez et al.
Introduction: Therapeutic apheresis (TA) is an extracorporeal technique used to treat various renal and non-renal pathologies, for which the ASFA guidelines provide recommendations. In Spain, nephrology services have prog...
Beyond the textbooks: Vacuolar cast as an emerging marker in urinary sediment [0.03%]
走出教科书：尿沉渣中新兴的标记物——空泡 casts 的临床意义
Oscar D Pons-Belda,Ana Calbet-Tur,Paloma Livianos-Arias-Camison et al.
Oscar D Pons-Belda et al.
What is the clinical impact of using EKFC equation for estimating glomerular filtration rate by creatinine in kidney transplant recipients? [0.03%]
估算移植受者的肾小球滤过率时使用EKFC方程有什么临床影响？
Miguel Martínez-Belotto,María José Ortega,Covadonga López Del Moral et al.
Miguel Martínez-Belotto et al.
Background and objective: Chronic kidney disease (CKD) is a prevalent condition, typically assessed using indirect markers such as estimated glomerular filtration rate (eGFR). The CKDEPI-2009 equation has been the most wi...
Efficacy of iptacopan in idiopathic immune complex-mediated membranoproliferative glomerulonephritis refractory to conventional treatment [0.03%]
Iptacopan治疗难治性特发免疫复合物介导的膜增生性肾小球肾炎疗效良好
Raquel López Hidalgo,Mercedes Caba Molina,Francisco Javier Ruiz Escolano et al.
Raquel López Hidalgo et al.
Membranoproliferative glomerulonephritis due to immune complexes (MPGN-IC) idiopathic is a diagnosis of exclusion, made after ruling out the most common etiological processes associated with this pattern of glomerular injury (infectious, au...
Case Reports
Nefrologia. 2026 Feb 12:501426. DOI:10.1016/j.nefroe.2026.501426 2026
Fibrillary glomerulonephritis: clinicopathological characteristics and treatment in a spanish tertiary center [0.03%]
西班牙一家三级医疗中心的纤维性肾小球肾炎的临床病理特征和治疗
Efraín Tatis,Natalia Ramos Terrades,María Alejandra Gabaldón et al.
Efraín Tatis et al.
Introduction: Fibrillary glomerulonephritis (FGN) has a poor prognosis and lacks standardized treatment. In this study, we describe clinicopathological characteristics, clinical course, and management of patients with FGN...