日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Psychosocial Assessment of Candidates for Transplantation (PACT) Score Identifies High Risk Patients in Pediatric Renal Transplantation

儿童肾移植候选者心理社会评估(PACT)评分可识别高危患者

Freischlag, Kyle W; Chen, Vivian; Nagaraj, Shashi K; Chua, Annabelle N; Chen, Dongfeng; Wigfall, Delbert R; Foreman, John W; Gbadegesin, Rasheed; Vikraman, Deepak; Chambers, Eileen T

Efficacy of antibiotic prophylaxis in children with vesicoureteral reflux: systematic review and meta-analysis

儿童膀胱输尿管反流抗生素预防疗效:系统评价和荟萃分析

Wang, Hsin-Hsiao S; Gbadegesin, Rasheed A; Foreman, John W; Nagaraj, Shashi K; Wigfall, Delbert R; Wiener, John S; Routh, Jonathan C

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.

kelch-like 3 和 cullin 3 的突变会导致高血压和电解质异常

Boyden Lynn M, Choi Murim, Choate Keith A, Nelson-Williams Carol J, Farhi Anita, Toka Hakan R, Tikhonova Irina R, Bjornson Robert, Mane Shrikant M, Colussi Giacomo, Lebel Marcel, Gordon Richard D, Semmekrot Ben A, Poujol Alain, Välimäki Matti J, De Ferrari Maria E, Sanjad Sami A, Gutkin Michael, Karet Fiona E, Tucci Joseph R, Stockigt Jim R, Keppler-Noreuil Kim M, Porter Craig C, Anand Sudhir K, Whiteford Margo L, Davis Ira D, Dewar Stephanie B, Bettinelli Alberto, Fadrowski Jeffrey J, Belsha Craig W, Hunley Tracy E, Nelson Raoul D, Trachtman Howard, Cole Trevor R P, Pinsk Maury, Bockenhauer Detlef, Shenoy Mohan, Vaidyanathan Priya, Foreman John W, Rasoulpour Majid, Thameem Farook, Al-Shahrouri Hania Z, Radhakrishnan Jai, Gharavi Ali G, Goilav Beatrice, Lifton Richard P

Hypercalcemia, hypercalciuria, and elevated calcitriol concentrations with autosomal dominant transmission due to CYP24A1 mutations: effects of ketoconazole therapy

由CYP24A1基因突变引起的常染色体显性遗传性高钙血症、高钙尿症和骨化三醇浓度升高:酮康唑治疗的影响

Tebben, Peter J; Milliner, Dawn S; Horst, Ronald L; Harris, Peter C; Singh, Ravinder J; Wu, Yanhong; Foreman, John W; Chelminski, Paul R; Kumar, Rajiv

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination

编码反向蛋白的INVS基因突变会导致2型肾痨,将肾囊性疾病与原发性纤毛功能和左右轴决定联系起来。

Otto, Edgar A; Schermer, Bernhard; Obara, Tomoko; O'Toole, John F; Hiller, Karl S; Mueller, Adelheid M; Ruf, Rainer G; Hoefele, Julia; Beekmann, Frank; Landau, Daniel; Foreman, John W; Goodship, Judith A; Strachan, Tom; Kispert, Andreas; Wolf, Matthias T; Gagnadoux, Marie F; Nivet, Hubert; Antignac, Corinne; Walz, Gerd; Drummond, Iain A; Benzing, Thomas; Hildebrandt, Friedhelm