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

247 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Perinatal renal disease.
Chitty LS, Woolf AS. Chitty LS, et al. Among authors: woolf as. Semin Fetal Neonatal Med. 2008 Jun;13(3):117. doi: 10.1016/j.siny.2007.10.004. Epub 2007 Dec 21. Semin Fetal Neonatal Med. 2008. PMID: 18160356 No abstract available.
Perspectives on human perinatal renal tract disease.
Woolf AS. Woolf AS. Semin Fetal Neonatal Med. 2008 Jun;13(3):196-201. doi: 10.1016/j.siny.2007.10.001. Epub 2007 Nov 13. Semin Fetal Neonatal Med. 2008. PMID: 17993294 Review.
Renal tract malformations: perspectives for nephrologists.
Kerecuk L, Schreuder MF, Woolf AS. Kerecuk L, et al. Among authors: woolf as. Nat Clin Pract Nephrol. 2008 Jun;4(6):312-25. doi: 10.1038/ncpneph0807. Epub 2008 Apr 29. Nat Clin Pract Nephrol. 2008. PMID: 18446149 Review.
Evolving concepts in human renal dysplasia.
Woolf AS, Price KL, Scambler PJ, Winyard PJ. Woolf AS, et al. J Am Soc Nephrol. 2004 Apr;15(4):998-1007. doi: 10.1097/01.asn.0000113778.06598.6f. J Am Soc Nephrol. 2004. PMID: 15034102 Review.
Mutation analyses of Uroplakin II in children with renal tract malformations.
Jenkins D, Bitner-Glindzicz M, Malcolm S, Allison J, de Bruyn R, Flanagan S, Thomas DF, Belk RA, Feather SA, Bingham C, Southgate J, Woolf AS. Jenkins D, et al. Among authors: woolf as. Nephrol Dial Transplant. 2006 Dec;21(12):3415-21. doi: 10.1093/ndt/gfl465. Epub 2006 Sep 29. Nephrol Dial Transplant. 2006. PMID: 17012268
Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred.
Kerecuk L, Sajoo A, McGregor L, Berg J, Haq MR, Sebire NJ, Bingham C, Edghill EL, Ellard S, Taylor J, Rigden S, Flinter FA, Woolf AS. Kerecuk L, et al. Among authors: woolf as. Nephrol Dial Transplant. 2007 Jan;22(1):259-63. doi: 10.1093/ndt/gfl531. Epub 2006 Sep 23. Nephrol Dial Transplant. 2007. PMID: 16998226 No abstract available.
247 results