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

Year Number of Results
1997 1
1999 5
2001 1
2004 1
2006 2
2007 2
2009 1
2010 2
2011 4
2012 7
2013 5
2014 5
2015 4
2016 5
2017 7
2018 3
2019 5
2020 5
2021 4
2022 4
2023 7
2024 1

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72 results

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Page 1
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe.
Nowotny H, Neumann U, Tardy-Guidollet V, Ahmed SF, Baronio F, Battelino T, Bertherat J, Blankenstein O, Bonomi M, Bouvattier C, Brac de la Perrière A, Brucker S, Cappa M, Chanson P, Claahsen-van der Grinten HL, Colao A, Cools M, Davies JH, Dörr HG, Fenske WK, Ghigo E, Giordano R, Gravholt CH, Huebner A, Husebye ES, Igbokwe R, Juul A, Kiefer FW, Léger J, Menassa R, Meyer G, Neocleous V, Phylactou LA, Rohayem J, Russo G, Scaroni C, Touraine P, Unger N, Vojtková J, Yeste D, Lajic S, Reisch N. Nowotny H, et al. Among authors: neocleous v. Eur J Endocrinol. 2022 Mar 23;186(5):K17-K24. doi: 10.1530/EJE-21-0554. Eur J Endocrinol. 2022. PMID: 35235536 Free PMC article.
Methylation status of hypothalamic Mkrn3 promoter across puberty.
Fanis P, Morrou M, Tomazou M, Michailidou K, Spyrou GM, Toumba M, Skordis N, Neocleous V, Phylactou LA. Fanis P, et al. Among authors: neocleous v. Front Endocrinol (Lausanne). 2023 Jan 13;13:1075341. doi: 10.3389/fendo.2022.1075341. eCollection 2022. Front Endocrinol (Lausanne). 2023. PMID: 36714607 Free PMC article.
Pathogenic and Low-Frequency Variants in Children With Central Precocious Puberty.
Neocleous V, Fanis P, Toumba M, Gorka B, Kousiappa I, Tanteles GA, Iasonides M, Nicolaides NC, Christou YP, Michailidou K, Nicolaou S, Papacostas SS, Christoforidis A, Kyriakou A, Vlachakis D, Skordis N, Phylactou LA. Neocleous V, et al. Front Endocrinol (Lausanne). 2021 Sep 24;12:745048. doi: 10.3389/fendo.2021.745048. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 34630334 Free PMC article.
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.
Evidence of digenic inheritance in autoinflammation-associated genes.
Neocleous V, Byrou S, Toumba M, Costi C, Shammas C, Kyriakou C, Christophidou-Anastasiadou V, Tanteles GA, Hadjipanayis A, Phylactou LA. Neocleous V, et al. J Genet. 2016 Dec;95(4):761-766. doi: 10.1007/s12041-016-0691-5. J Genet. 2016. PMID: 27994174 Free article.
72 results