Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2014 | 2 |
2015 | 3 |
2016 | 2 |
2017 | 1 |
2024 | 0 |
Search Results
6 results
Results by year
Filters applied: . Clear all
Page 1
Genetics of childhood steroid-sensitive nephrotic syndrome.
Pediatr Nephrol. 2017 Sep;32(9):1481-1488. doi: 10.1007/s00467-016-3456-8. Epub 2016 Jul 29.
Pediatr Nephrol. 2017.
PMID: 27470160
Free PMC article.
Review.
The Genetics of Nephrotic Syndrome.
Rheault MN, Gbadegesin RA.
Rheault MN, et al.
J Pediatr Genet. 2016 Mar;5(1):15-24. doi: 10.1055/s-0035-1557109. Epub 2015 Aug 13.
J Pediatr Genet. 2016.
PMID: 27617138
Free PMC article.
Review.
Item in Clipboard
AKI in Children Hospitalized with Nephrotic Syndrome.
Rheault MN, Zhang L, Selewski DT, Kallash M, Tran CL, Seamon M, Katsoufis C, Ashoor I, Hernandez J, Supe-Markovina K, D'Alessandri-Silva C, DeJesus-Gonzalez N, Vasylyeva TL, Formeck C, Woll C, Gbadegesin R, Geier P, Devarajan P, Carpenter SL, Kerlin BA, Smoyer WE; Midwest Pediatric Nephrology Consortium.
Rheault MN, et al.
Clin J Am Soc Nephrol. 2015 Dec 7;10(12):2110-8. doi: 10.2215/CJN.06620615. Epub 2015 Oct 8.
Clin J Am Soc Nephrol. 2015.
PMID: 26450933
Free PMC article.
Item in Clipboard
Variability in phenotype induced by the podocin variant R229Q plus a single pathogenic mutation.
Phelan PJ, Hall G, Wigfall D, Foreman J, Nagaraj S, Malone AF, Winn MP, Howell DN, Gbadegesin R.
Phelan PJ, et al.
Clin Kidney J. 2015 Oct;8(5):538-42. doi: 10.1093/ckj/sfv063. Epub 2015 Jul 20.
Clin Kidney J. 2015.
PMID: 26413278
Free PMC article.
Item in Clipboard
Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.
Gbadegesin RA, Hall G, Adeyemo A, Hanke N, Tossidou I, Burchette J, Wu G, Homstad A, Sparks MA, Gomez J, Jiang R, Alonso A, Lavin P, Conlon P, Korstanje R, Stander MC, Shamsan G, Barua M, Spurney R, Singhal PC, Kopp JB, Haller H, Howell D, Pollak MR, Shaw AS, Schiffer M, Winn MP.
Gbadegesin RA, et al.
J Am Soc Nephrol. 2014 Sep;25(9):1991-2002. doi: 10.1681/ASN.2013090976. Epub 2014 Mar 27.
J Am Soc Nephrol. 2014.
PMID: 24676636
Free PMC article.
Item in Clipboard
Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis.
Malone AF, Phelan PJ, Hall G, Cetincelik U, Homstad A, Alonso AS, Jiang R, Lindsey TB, Wu G, Sparks MA, Smith SR, Webb NJ, Kalra PA, Adeyemo AA, Shaw AS, Conlon PJ, Jennette JC, Howell DN, Winn MP, Gbadegesin RA.
Malone AF, et al.
Kidney Int. 2014 Dec;86(6):1253-9. doi: 10.1038/ki.2014.305. Epub 2014 Sep 17.
Kidney Int. 2014.
PMID: 25229338
Free PMC article.
Item in Clipboard
Cite
Cite