Sulfate handling in proximal renal tubular defects: an exploratory study [0.03%]
近端肾小管功能不全的硫酸盐处理：一项探索性研究
Emil den Bakker,Miriam Wamelink,Desiree E C Smith et al.
Emil den Bakker et al.
Background: Renal tubular disease causes loss of electrolytes and other molecules. One of these electrolytes is inorganic sulfate, which is reabsorbed by dedicated transporters, including NaS1, encoded by the SLC13A1 gene...
Cystic burden meets blood pressure: cardiac remodelling in paediatric autosomal dominant polycystic kidney disease [0.03%]
囊肿负担遇到血压：儿童常染色体显性多囊肾病中心脏重塑
Camille Heming,Emily Haseler,Alexandra Savis et al.
Camille Heming et al.
Background: We evaluated the prevalence and phenotype of hypertension in untreated children with autosomal dominant polycystic kidney disease (ADPKD) and examined associations with blood pressure (BP), cyst burden, and le...
Correction: Longitudinal hemodialysis access pressure trends as a predictor of arteriovenous fistula compromise in children [0.03%]
纠正：长期血液透析压力趋势作为预测儿童动静脉瘘并发症的指标
Salar Bani Hani,Raymond Quigley
Salar Bani Hani
Published Erratum
Pediatric nephrology (Berlin, Germany). 2026 May 18. DOI:10.1007/s00467-026-07350-2 2026
Thrombotic microangiopathy-like acute kidney injury revealing a germline GATA1 mutation in a child with inherited cytopenia [0.03%]
一名患有遗传性血细胞减少症的儿童出现类似血栓性微血管病的急性肾损伤并被发现GATA1基因 germline突变
Amal E Gohary,Doaa M Youssef,Diana Hanna et al.
Amal E Gohary et al.
Thrombotic microangiopathy (TMA) is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and organ injury, most commonly acute kidney injury (AKI). It may occur as a primary complement‑mediated disorder or secondary to oth...
Novel use of the Nuwellis® dual extended length catheter (dELC) as umbilical venous access for neonatal kidney replacement therapy: case series [0.03%]
Nuwellis®双延长导管(dELC)作为新生儿脐静脉通路进行肾脏替代治疗的新型应用：病例系列报告
Kara Short,Alyssa Umberger,Meggie Mathis et al.
Kara Short et al.
Background: Neonates with congenital kidney failure or acute kidney injury often require continuous kidney replacement therapy (CKRT). Historically, venous access for CKRT in this population has relied on non-approved adu...
The population frequency of predicted pathogenic genetic variants in commonly affected CAKUT genes in the general population [0.03%]
一般人群中常见CAKUT基因预测致病性遗传变异的群体频率
Mary Huang,Judy Savige
Mary Huang
Background: Renal imaging suggests that congenital anomalies of the kidney and urinary tract (CAKUT) affect one in 200 of the population, and 20% have a monogenic cause. This study determined the population frequency of p...
Ambulatory blood pressure abnormalities, obstructive sleep apnea, and end-organ damage in children with sickle cell disease [0.03%]
血红蛋白SC病患者的日间血压异常、阻塞性睡眠呼吸暂停和靶器官损伤
Harshitha S,Athira Puthukara,Amber Kumar et al.
Harshitha S et al.
Background: Many individuals with sickle cell disease (SCD) survive into adulthood, posing a challenge in managing and preventing damage to vital organs such as the heart and kidneys. Studies on hypertension in this popul...
Relapsing childhood steroid sensitive nephrotic syndrome: what determines eventual remission? [0.03%]
儿童反复发作的肾病综合征：什么决定最终缓解？
Evgenia Gurevich,Daniel Landau
Evgenia Gurevich
Background: Childhood idiopathic nephrotic syndrome (INS) responds to corticosteroids (CS), but tends to relapse, often requiring steroid sparing agents (SSA). Long standing treatment free remission (LTFR) evolves in most...
Kidney calcifications and fluid-electrolyte imbalances in cystic fibrosis: a simplified synopsis [0.03%]
囊性纤维化患者的肾脏钙化和电解质紊乱：简明综述
Simone Janett,Martin Scoglio,Massimiliano Bertacchi et al.
Simone Janett et al.