26 results on '"Gbadegesin, Rasheed A"'
Search Results
2. Patient level factors increase risk of acute kidney disease in hospitalized children with acute kidney injury
3. Inaxaplin for the treatment of APOL1-associated kidney disease
4. Hiding in plain sight: genetics of childhood steroid-resistant nephrotic syndrome in Sub-Saharan Africa
5. Evolutionary genetics and acclimatization in nephrology
6. Kidney biopsy findings in children with sickle cell disease: a Midwest Pediatric Nephrology Consortium study
7. Correction to: Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings
8. Treatment of steroid-resistant nephrotic syndrome in the genomic era
9. Association of infections and venous thromboembolism in hospitalized children with nephrotic syndrome
10. Recurrence of nephrotic syndrome following kidney transplantation is associated with initial native kidney biopsy findings
11. Responsiveness of the PROMIS® measures to changes in disease status among pediatric nephrotic syndrome patients: a Midwest pediatric nephrology consortium study
12. Dysregulation of WTI (−KTS) is Associated with the Kidney-Specific Effects of the LMX1B R246Q Mutation
13. Genetics of childhood steroid-sensitive nephrotic syndrome
14. Vesicoureteral reflux and the extracellular matrix connection
15. Rare variants in tenascin genes in a cohort of children with primary vesicoureteric reflux
16. The impact of disease duration on quality of life in children with nephrotic syndrome: a Midwest Pediatric Nephrology Consortium study
17. Gaining the Patient Reported Outcomes Measurement Information System (PROMIS) perspective in chronic kidney disease: a Midwest Pediatric Nephrology Consortium study
18. Treatment outcome of late steroid-resistant nephrotic syndrome: a study by the Midwest Pediatric Nephrology Consortium
19. Gaining the PROMIS perspective from children with nephrotic syndrome: a Midwest pediatric nephrology consortium study
20. Genetic testing in nephrotic syndrome—challenges and opportunities
21. Pathogenesis and therapy of focal segmental glomerulosclerosis: an update
22. Significance of hemolysis on extracorporeal life support after cardiac surgery in children
23. Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS
24. Low prevalence of NPHS2 mutations in African American children with steroid-resistant nephrotic syndrome
25. Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome
26. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible
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