Interpreting subclinical atherosclerosis in children with nephrotic syndrome: beyond between-group differences [0.03%]
儿童肾病综合征亚临床动脉硬化解读：超越组间差异的观点
Hongxiao Gao,Tongyuan Zhang
Hongxiao Gao
Emily Akerman,Amélie Cifuentes,Guillaume Courbon
Emily Akerman
Patients with kidney disease face a markedly increased risk of developing cardiovascular disease (CVD) which manifests in multiple forms, including: left ventricular hypertrophy, heart failure, atherosclerosis, and vascular inflammation, al...
Young adults born moderately to extremely preterm have higher eGFR and cystatin C compared to young adults born at term [0.03%]
极早产至中度早产出生的青年人其eGFR和Cys-C水平高于足月出生的青年人
Tyler T Shimfessel,Gregory P Barton,Keri A Drake et al.
Tyler T Shimfessel et al.
Background: Adolescents and adults born preterm are at increased risk for kidney dysfunction, possibly secondary to incomplete nephrogenesis. However, few long-term follow-up studies are available from U.S.-born preterm c...
When should sequential rituximab therapy for long-term B-cell depletion be initiated in children with steroid-sensitive nephrotic syndrome? [0.03%]
糖皮质激素敏感型肾病综合征患儿的序贯利妥昔单抗治疗应在何时开始以实现长期B细胞耗竭？
Shuichiro Fujinaga,Takahiro Ono,Aya Saito
Shuichiro Fujinaga
Elevated serum creatinine over the first week of life and mortality risk in extremely preterm neonates: a secondary analysis of the Preterm Erythropoietin Neuroprotection Trial (PENUT) [0.03%]
出生后第一周内血清肌酐升高与极早产新生儿的死亡风险：Preterm Erythropoietin Neuroprotection Trial试验的事后分析研究结果
Melissa S Zhou,Russell Griffin,David J Askenazi et al.
Melissa S Zhou et al.
Background: The neonatal-modified Kidney Disease: Improving Global Outcomes acute kidney injury (KDIGO-AKI) serum creatinine (SCr) definition is widely used to characterize neonatal AKI. In extremely preterm neonates born...
Comment on "A study of body composition, muscle strength, and arterial stiffness in adolescents with primary and secondary hypertension" [0.03%]
对“原发性和继发性高血压青少年体成分、肌肉力量及动脉僵硬特征的研究”一文的评论
Wendi Huang,Zhuoquan Wang
Wendi Huang
Prevention is better than cure: role of RAAS blockade in preventing catastrophic hypotension after bilateral native nephrectomies in infants [0.03%]
预防胜于治疗：雷公藤碱诱导的血小板凋亡及其相关信号通路的研究
Zainab Arslan,Natasha Baugh,Rukshana Shroff
Zainab Arslan
Clinical and molecular spectrum of primary hyperoxaluria type 1 in Tunisia: pediatric presentation and minimum observed prevalence [0.03%]
突尼斯原发性高草酸尿症1型的临床和分子谱系：儿科表现和最低观察到的患病率
Ridha M&#x;rad,Mahdi Kammoun,Ahlem Achour et al.
Ridha M&#x;rad et al.
Background: Primary hyperoxaluria type 1 (PH1) is a rare autosomal recessive disorder caused by pathogenic variants in the AGXT gene. In regions with a high prevalence of consanguinity, the burden of PH1 is expected to be...
Carolina Bigatti,Paolo Cravedi,Andrea Angeletti
Carolina Bigatti
Podocytopathies, including minimal change disease and focal segmental glomerulosclerosis, represent the leading causes of nephrotic syndrome in children and adolescents. Although traditionally considered T-cell-mediated disorders, growing e...
Clinical characteristics and genetic analyses of Korean children with Dent disease [0.03%]
韩国Dent病儿童的临床特征和基因分析
Eun Mi Yang,Yo Han Ahn,Ji Hyun Kim et al.
Eun Mi Yang et al.
Background: Dent disease is a hereditary kidney tubular disorder caused by pathogenic variants in either the CLCN5 (Dent disease 1) or OCRL1 (Dent disease 2) genes. As a rare genetic disorder, Dent disease often presents ...