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

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2009 6
2010 6
2011 6
2012 5
2013 13
2014 11
2015 9
2016 4
2017 7
2018 4
2019 3
2020 3
2021 5
2022 3
2023 5
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

73 results

Results by year

Filters applied: . Clear all
Page 1
Kidney-on-a-chip: untapped opportunities.
Ashammakhi N, Wesseling-Perry K, Hasan A, Elkhammas E, Zhang YS. Ashammakhi N, et al. Among authors: wesseling perry k. Kidney Int. 2018 Dec;94(6):1073-1086. doi: 10.1016/j.kint.2018.06.034. Epub 2018 Oct 23. Kidney Int. 2018. PMID: 30366681 Free PMC article. Review.
Gut microbiome, parathyroid hormone, and bone.
Kermgard E, Chawla NK, Wesseling-Perry K. Kermgard E, et al. Among authors: wesseling perry k. Curr Opin Nephrol Hypertens. 2021 Jul 1;30(4):418-423. doi: 10.1097/MNH.0000000000000714. Curr Opin Nephrol Hypertens. 2021. PMID: 34027903 Review.
Recurrent disease after pediatric renal transplantation.
Nayak A, Ettenger R, Wesseling-Perry K. Nayak A, et al. Among authors: wesseling perry k. Pediatr Transplant. 2024 May;28(3):e14676. doi: 10.1111/petr.14676. Pediatr Transplant. 2024. PMID: 38650536 Review.
The Authors Reply.
Wesseling-Perry K. Wesseling-Perry K. Kidney Int. 2015 Sep;88(3):640-1. doi: 10.1038/ki.2015.219. Kidney Int. 2015. PMID: 26323080 Free article. No abstract available.
Macrocephaly and developmental delay caused by missense variants in RAB5C.
Koop K, Yuan W, Tessadori F, Rodriguez-Polanco WR, Grubbs J, Zhang B, Osmond M, Graham G, Sawyer S, Conboy E, Vetrini F, Treat K, Płoski R, Pienkowski VM, Kłosowska A, Fieg E, Krier J, Mallebranche C, Alban Z, Aldinger KA, Ritter D, Macnamara E, Sullivan B, Herriges J, Alaimo JT, Helbig C, Ellis CA, van Eyk C, Gecz J, Farrugia D, Osei-Owusu I, Adès L, van den Boogaard MJ, Fuchs S, Bakker J, Duran K, Dawson ZD, Lindsey A, Huang H, Baldridge D, Silverman GA, Grant BD, Raizen D; Undiagnosed Diseases Network; van Haaften G, Pak SC, Rehmann H, Schedl T, van Hasselt P. Koop K, et al. Hum Mol Genet. 2023 Oct 17;32(21):3063-3077. doi: 10.1093/hmg/ddad130. Hum Mol Genet. 2023. PMID: 37552066 Free PMC article.
FGF-23 in bone biology.
Wesseling-Perry K. Wesseling-Perry K. Pediatr Nephrol. 2010 Apr;25(4):603-8. doi: 10.1007/s00467-009-1384-6. Epub 2009 Dec 15. Pediatr Nephrol. 2010. PMID: 20012997 Free PMC article. Review.
Bone disease in pediatric chronic kidney disease.
Wesseling-Perry K. Wesseling-Perry K. Pediatr Nephrol. 2013 Apr;28(4):569-76. doi: 10.1007/s00467-012-2324-4. Epub 2012 Oct 14. Pediatr Nephrol. 2013. PMID: 23064662 Free PMC article. Review.
73 results