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

Complexity and Health Care Utilization in Infant ESKD

婴儿终末期肾病的复杂性和医疗保健利用情况

Pudupakkam, Ashna R; Braun, Michael C; Joseph, Catherine; Srivaths, Poyyapakkam R; Swartz, Sarah J; Shah, Shweta S

Responding to the workforce crisis: consensus recommendations from the Second Workforce Summit of the American Society of Pediatric Nephrology

应对劳动力危机:美国儿科肾脏病学会第二次劳动力峰会的共识建议

Soranno, Danielle E; Amaral, Sandra; Ashoor, Isa; Atkinson, Meredith A; Barletta, Gina-Marie; Braun, Michael C; Carlson, Joann; Carter, Caitlin; Chua, Annabelle; Dharnidharka, Vikas R; Drake, Keri; Erkan, Elif; Feig, Dan; Goldstein, Stuart L; Hains, David; Harshman, Lyndsay A; Ingulli, Elizabeth; Kula, Alexander J; Leonard, Mary; Mannemuddhu, Sudha; Menon, Shina; Modi, Zubin J; Moxey-Mims, Marva; Nada, Arwa; Norwood, Victoria; Starr, Michelle C; Verghese, Priya S; Weidemann, Darcy; Weinstein, Adam; Smith, Jodi

Fetal Nephrology: A Quaternary Care Center Experience

胎儿肾脏病学:四级护理中心的经验

Plaud Gonzalez, Auda M; Joseph, Catherine; Stover, Samantha R; Nassr, Ahmed; Koh, Chester J; Angelo, Joseph R; Braun, Michael C

Compound heterozygosity of a de novo submicroscopic deletion and an inherited frameshift pathogenic variant in the PKHD1 gene in a fetus with bilaterally enlarged and echogenic kidneys, enlarged abdomen and oligohydramnios

胎儿PKHD1基因中存在新生亚显微缺失和遗传性移码致病变异的复合杂合性,表现为双侧肾脏增大且回声增强、腹部增大和羊水过少。

Sakyu, Takuya; Stover, Samantha R; Wang, Yue; Ward, Patricia; Gandhi, Manisha; Braun, Michael C; Van den Veyver, Ignatia B; Bi, Weimin

Lupus Nephritis, Autoantibody Production and Kidney Outcomes in Males with Childhood-Onset Systemic Lupus Erythematosus

儿童期发病系统性红斑狼疮男性患者的狼疮性肾炎、自身抗体产生和肾脏结局

Wenderfer, Scott E; Orjuela, Alvaro; Bekheirnia, Mir Reza; Pereira, Maria; Muscal, Eyal; Braun, Michael C; De Guzman, Marietta

Emerging Insights Into Chronic Renal Disease Pathogenesis in Hypertension From Human and Animal Genomic Studies

人类和动物基因组学研究对高血压慢性肾病发病机制的新见解

Dhande, Isha S; Braun, Michael C; Doris, Peter A

Clinical Utility of Genetic Testing in the Precision Diagnosis and Management of Pediatric Patients with Kidney and Urinary Tract Diseases

基因检测在儿童肾脏和泌尿系统疾病精准诊断和治疗中的临床应用

Bekheirnia, Nasim; Glinton, Kevin E; Rossetti, Linda; Manor, Joshua; Chen, Wuyan; Lamb, Dolores J; Braun, Michael C; Bekheirnia, Mir Reza

DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract

DYRK1A相关智力障碍:一种与肾脏和泌尿系统先天性异常相关的综合征

Blackburn, Alexandria T M; Bekheirnia, Nasim; Uma, Vanessa C; Corkins, Mark E; Xu, Yuxiao; Rosenfeld, Jill A; Bainbridge, Matthew N; Yang, Yaping; Liu, Pengfei; Madan-Khetarpal, Suneeta; Delgado, Mauricio R; Hudgins, Louanne; Krantz, Ian; Rodriguez-Buritica, David; Wheeler, Patricia G; Al-Gazali, Lihadh; Mohamed Saeed Mohamed Al Shamsi, Aisha; Gomez-Ospina, Natalia; Chao, Hsiao-Tuan; Mirzaa, Ghayda M; Scheuerle, Angela E; Kukolich, Mary K; Scaglia, Fernando; Eng, Christine; Willsey, Helen Rankin; Braun, Michael C; Lamb, Dolores J; Miller, Rachel K; Bekheirnia, Mir Reza

Germ-line genetic variation in the immunoglobulin heavy chain creates stroke susceptibility in the spontaneously hypertensive rat

免疫球蛋白重链的种系遗传变异导致自发性高血压大鼠易患中风。

Dhande, Isha S; Kneedler, Sterling C; Joshi, Aniket S; Zhu, Yaming; Hicks, M John; Wenderfer, Scott E; Braun, Michael C; Doris, Peter A

Peritoneal dialysis catheter outcomes in infants initiating peritoneal dialysis for end-stage renal disease

终末期肾病患儿开始接受腹膜透析治疗时,腹膜透析导管的使用情况

Imani, Peace D; Carpenter, Jennifer L; Bell, Cynthia S; Brandt, Mary L; Braun, Michael C; Swartz, Sarah J