 |
|
Genetic tests in children with steroid-resistant nephrotic syndrome
Hae Il Cheong
Kidney Res Clin Pract. 2020;39(1):7-16. Published online 2020 Mar 31 DOI: https://doi.org/10.23876/j.krcp.20.001
|
|
Citations to this article as recorded by
 NPHS1 Gene Mutations in Children with Focal Segmental Glomerulosclerosis and Literature Review
玉婷 李
Advances in Clinical Medicine.2024; 14(02): 3037. CrossRef Predicting the efficacy of glucocorticoids in pediatric primary immune thrombocytopenia using plasma proteomics
Qingqing Cao, Haiyan Zhu, Wei Xu, Rongrong Zhang, Yun Wang, Zhaofang Tian, Yufang Yuan
Frontiers in Immunology.2023;[Epub] CrossRef Efficacy of rituximab therapy in children with nephrotic syndrome: a 10-year experience from an Iranian pediatric hospital
Behnaz Bazargani, Zahra Noparast, Leila Khedmat, Daryoosh Fahimi, Seyed Taher Esfahani, Mastaneh Moghtaderi, Arash Abbasi, Azadeh Afshin, Sayed Yousef Mojtahedi
BMC Pediatrics.2022;[Epub] CrossRef A Family Segregating Lethal Primary Coenzyme Q10 Deficiency Due to Two Novel COQ6 Variants
Na Wang, Youmin Zheng, Lingzi Zhang, Xiong Tian, Yicheng Fang, Ming Qi, Juping Du, Shuaishuai Chen, Shiyong Chen, Jun Li, Bo Shen, Lizhen Wang
Frontiers in Genetics.2022;[Epub] CrossRef Spectrum of NPHS1 and NPHS2 variants in egyptian children with focal segmental glomerular sclerosis: identification of six novel variants and founder effect
Manal M. Thomas, Heba Mostafa Ahmed, Sara H. El-Dessouky, Abeer Ramadan, Osama Ezzat Botrous, Mohamed S. Abdel-Hamid
Molecular Genetics and Genomics.2022; 297(3): 689. CrossRef Whole-exome sequencing of a multicenter cohort identifies genetic changes associated with clinical phenotypes in pediatric nephrotic syndrome
Jia Jiao, Li Wang, Fenfen Ni, Mo Wang, Shipin Feng, Xiaojie Gao, Han Chan, Xueying Yang, Hao Lee, Huan Chi, Xuelan Chen, Daoqi Wu, Gaofu Zhang, Baohui Yang, Anshuo Wang, Qin Yang, Junli Wan, Sijie Yu, Xiaoqin Li, Mei Wang, Xiaofeng Chen, Xianying Mai, Xio
Genes & Diseases.2022; 9(6): 1662. CrossRef Steroidresistant nephrotic syndrome in a child associated with a mutation in the INF2 gene
N. S. Zhuravleva, Т. A. Frayfeld, O. A. Vorobieva, A. S. Telina, N. Yu. Mineeva
Ural Medical Journal.2022; 21(3): 107. CrossRef Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis
China Nagano, Shigeo Hara, Norishige Yoshikawa, Asami Takeda, Yoshimitsu Gotoh, Riku Hamada, Kentaro Matsuoka, Masaki Yamamoto, Shuichiro Fujinaga, Koji Sakuraya, Koichi Kamei, Yuko Hamasaki, Hideyo Oguchi, Yoshinori Araki, Yayoi Ogawa, Takayuki Okamoto,
Kidney360.2022; 3(8): 1384. CrossRef Uptake of next‐generation sequencing in children with end‐stage renal disease secondary to focal segmental glomerulosclerosis and parental decision for kidney transplantation—Experience from a low resource setting: A Retrospective Cohort Study
Rajiv Sinha, Subhankar Sarkar, Kausik Mandal, Yincent Tse
Pediatric Transplantation.2021;[Epub] CrossRef Clinical Genetic Testing in Children with Kidney Disease
Eungu Kang, Beom Hee Lee
Childhood Kidney Diseases.2021; 25(1): 14. CrossRef Steroid-resistant Nephrotic Syndrome in Children: A Mini-review on Genetic Mechanisms, Predictive Biomarkers and Pharmacotherapy Strategies
Hong-Li Guo, Ling Li, Ze-Yue Xu, Xia Jing, Ying Xia, Jin-Chun Qiu, Xing Ji, Feng Chen, Jing Xu, Fei Zhao
Current Pharmaceutical Design.2021; 27(2): 319. CrossRef Regulation of the Actin Cytoskeleton in Podocytes
Judith Blaine, James Dylewski
Cells.2020; 9(7): 1700. CrossRef Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis
Eujin Park, Chung Lee, Nayoung Kim, Yo Ahn, Young Park, Joo Lee, Seong Kim, Min Cho, Heeyeon Cho, Kee Yoo, Jae Shin, Hee Kang, Il-Soo Ha, Woong-Yang Park, Hae Cheong
Journal of Clinical Medicine.2020; 9(6): 2013. CrossRef
|