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

Year Number of Results
2006 2
2007 1
2008 3
2009 4
2011 2
2013 3
2014 3
2015 4
2016 8
2017 4
2018 3
2019 7
2020 8
2021 4
2022 12
2023 1
2024 0

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62 results

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Page 1
Ubiquitin-proteasome system in diabetic retinopathy.
Svikle Z, Peterfelde B, Sjakste N, Baumane K, Verkauskiene R, Jeng CJ, Sokolovska J. Svikle Z, et al. Among authors: verkauskiene r. PeerJ. 2022 Jul 19;10:e13715. doi: 10.7717/peerj.13715. eCollection 2022. PeerJ. 2022. PMID: 35873915 Free PMC article. Review.
Congenital hyperinsulinism.
Petraitienė I, Barauskas G, Gulbinas A, Malcius D, Hussain K, Verkauskas G, Verkauskienė R. Petraitienė I, et al. Among authors: verkauskiene r. Medicina (Kaunas). 2014;50(3):190-5. doi: 10.1016/j.medici.2014.08.006. Epub 2014 Aug 13. Medicina (Kaunas). 2014. PMID: 25323548 Free article. Review.
The current management of Turner Syndrome.
Kriksciuniene R, Zilaitiene B, Verkauskiene R. Kriksciuniene R, et al. Among authors: verkauskiene r. Minerva Endocrinol. 2016 Mar;41(1):105-21. Minerva Endocrinol. 2016. PMID: 26878561 Review.
Puberty in children born small for gestational age.
Verkauskiene R, Petraitiene I, Albertsson Wikland K. Verkauskiene R, et al. Horm Res Paediatr. 2013;80(2):69-77. doi: 10.1159/000353759. Epub 2013 Jul 26. Horm Res Paediatr. 2013. PMID: 23899516 Free article. Review.
Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
Eggermann T, Elbracht M, Kurth I, Juul A, Johannsen TH, Netchine I, Mastorakos G, Johannsson G, Musholt TJ, Zenker M, Prawitt D, Pereira AM, Hiort O; European Reference Network on Rare Endocrine Conditions (ENDO-ERN. Eggermann T, et al. Orphanet J Rare Dis. 2020 Jun 8;15(1):144. doi: 10.1186/s13023-020-01420-w. Orphanet J Rare Dis. 2020. PMID: 32513286 Free PMC article. Review.
62 results