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Page 1
COVID-19 in Children With Kidney Disease: A Report of 2 Cases.
Basalely A, Brathwaite K, Duong MD, Liu D, Mazo A, Xie Y, Del Rio M, Goilav B, Hayde N, Kaskel FJ, Zolotnitskaya A, Reidy KJ. Basalely A, et al. Among authors: zolotnitskaya a. Kidney Med. 2021 Jan-Feb;3(1):120-123. doi: 10.1016/j.xkme.2020.09.007. Epub 2020 Nov 21. Kidney Med. 2021. PMID: 33251504 Free PMC article.
Renal function and proteinuria after successful immunosuppressive therapies in patients with FSGS.
Hogg RJ, Friedman A, Greene T, Radeva M, Budisavljevic MN, Gassman J, Gipson DS, Jefferson JA, John EG, Kaskel FJ, Moudgil A, Moxey-Mims M, Ortiz LA, Schelling JR, Schnaper W, Srivastava T, Trachtman H, Vehaskari VM, Wong C, Woronieki RP, Van Why SK, Zolotnitskaya A. Hogg RJ, et al. Among authors: zolotnitskaya a. Clin J Am Soc Nephrol. 2013 Feb;8(2):211-8. doi: 10.2215/CJN.08330812. Epub 2012 Nov 8. Clin J Am Soc Nephrol. 2013. PMID: 23143503 Free PMC article. Clinical Trial.
A 5-year-old girl with kidney impairment and severe anemia: Questions.
Steinman B, Del Rio M, Zolotnitskaya A, Hayde N. Steinman B, et al. Among authors: zolotnitskaya a. Pediatr Nephrol. 2023 Feb;38(2):391-392. doi: 10.1007/s00467-022-05586-2. Epub 2022 Jun 13. Pediatr Nephrol. 2023. PMID: 35695958 No abstract available.
A 5-year-old girl with kidney impairment and severe anemia: Answers.
Steinman B, Del Rio M, Zolotnitskaya A, Hayde N. Steinman B, et al. Among authors: zolotnitskaya a. Pediatr Nephrol. 2023 Feb;38(2):393-396. doi: 10.1007/s00467-022-05608-z. Epub 2022 Jun 13. Pediatr Nephrol. 2023. PMID: 35695962 No abstract available.
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.
Lovric S, Fang H, Vega-Warner V, Sadowski CE, Gee HY, Halbritter J, Ashraf S, Saisawat P, Soliman NA, Kari JA, Otto EA, Hildebrandt F; Nephrotic Syndrome Study Group. Lovric S, et al. Clin J Am Soc Nephrol. 2014 Jun 6;9(6):1109-16. doi: 10.2215/CJN.09010813. Epub 2014 Apr 17. Clin J Am Soc Nephrol. 2014. PMID: 24742477 Free PMC article.
Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations.
Chernin G, Vega-Warner V, Schoeb DS, Heeringa SF, Ovunc B, Saisawat P, Cleper R, Ozaltin F, Hildebrandt F; Members of the GPN Study Group. Chernin G, et al. Clin J Am Soc Nephrol. 2010 Sep;5(9):1655-62. doi: 10.2215/CJN.09351209. Epub 2010 Jul 1. Clin J Am Soc Nephrol. 2010. PMID: 20595692 Free PMC article.
12 results