Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

109 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
GAPVD1 and ANKFY1 Mutations Implicate RAB5 Regulation in Nephrotic Syndrome.
Hermle T, Schneider R, Schapiro D, Braun DA, van der Ven AT, Warejko JK, Daga A, Widmeier E, Nakayama M, Jobst-Schwan T, Majmundar AJ, Ashraf S, Rao J, Finn LS, Tasic V, Hernandez JD, Bagga A, Jalalah SM, El Desoky S, Kari JA, Laricchia KM, Lek M, Rehm HL, MacArthur DG, Mane S, Lifton RP, Shril S, Hildebrandt F. Hermle T, et al. Among authors: finn ls. J Am Soc Nephrol. 2018 Aug;29(8):2123-2138. doi: 10.1681/ASN.2017121312. Epub 2018 Jun 29. J Am Soc Nephrol. 2018. PMID: 29959197 Free PMC article.
COQ2 nephropathy: a treatable cause of nephrotic syndrome in children.
Starr MC, Chang IJ, Finn LS, Sun A, Larson AA, Goebel J, Hanevold C, Thies J, Van Hove JLK, Hingorani SR, Lam C. Starr MC, et al. Among authors: finn ls. Pediatr Nephrol. 2018 Jul;33(7):1257-1261. doi: 10.1007/s00467-018-3937-z. Epub 2018 Apr 10. Pediatr Nephrol. 2018. PMID: 29637272 Free PMC article.
Nephrotic syndrome in the newborn.
Finn LS, Symons JM, Smith JM. Finn LS, et al. Am J Kidney Dis. 2003 Dec;42(6):1318-23. doi: 10.1053/j.ajkd.2003.08.041. Am J Kidney Dis. 2003. PMID: 14655207 No abstract available.
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis).
Doherty D, Parisi MA, Finn LS, Gunay-Aygun M, Al-Mateen M, Bates D, Clericuzio C, Demir H, Dorschner M, van Essen AJ, Gahl WA, Gentile M, Gorden NT, Hikida A, Knutzen D, Ozyurek H, Phelps I, Rosenthal P, Verloes A, Weigand H, Chance PF, Dobyns WB, Glass IA. Doherty D, et al. Among authors: finn ls. J Med Genet. 2010 Jan;47(1):8-21. doi: 10.1136/jmg.2009.067249. Epub 2009 Jul 1. J Med Genet. 2010. PMID: 19574260 Free PMC article.
Urinary elafin and kidney injury in hematopoietic cell transplant recipients.
Hingorani S, Finn LS, Pao E, Lawler R, Schoch G, McDonald GB, Najafian B, Sandmaier B, Gooley T. Hingorani S, et al. Among authors: finn ls. Clin J Am Soc Nephrol. 2015 Jan 7;10(1):12-20. doi: 10.2215/CJN.01840214. Epub 2014 Nov 11. Clin J Am Soc Nephrol. 2015. PMID: 25388519 Free PMC article.
Polyomavirus nephropathy in pediatric kidney transplant recipients.
Smith JM, McDonald RA, Finn LS, Healey PJ, Davis CL, Limaye AP. Smith JM, et al. Among authors: finn ls. Am J Transplant. 2004 Dec;4(12):2109-17. doi: 10.1111/j.1600-6143.2004.00629.x. Am J Transplant. 2004. PMID: 15575916 Free article.
109 results