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Detection of hepatocyte nuclear factor 4A(HNF4A) gene variant as the cause for congenital hyperinsulinism leads to revision of the diagnosis of the mother.
Vlachopapadopoulou EA, Dikaiakou E, Fotiadou A, Sifianou P, Tatsi EB, Sertedaki A, Kanaka-Gantenbein C, Michalacos S. Vlachopapadopoulou EA, et al. Among authors: fotiadou a. J Pediatr Endocrinol Metab. 2020 Oct 8;34(4):527-530. doi: 10.1515/jpem-2020-0302. Print 2021 Apr 27. J Pediatr Endocrinol Metab. 2020. PMID: 33031054
Mönckeberg sclerosis in patients with thyroid papillary carcinoma.
Venetsanaki V, Zisimopoulou E, Zouli C, Boudina M, Gkiouras K, Xirou P, Fotiadou A, Stamati M, Argyropoulou E, Chrisoulidou A. Venetsanaki V, et al. Among authors: fotiadou a. Endocr Oncol. 2024 May 2;4(1):e230047. doi: 10.1530/EO-23-0047. eCollection 2024 Jan 1. Endocr Oncol. 2024. PMID: 38770191 Free PMC article.
A Rare Manifestation of Secondary Hyperparathyroidism Due to Brown Tumors: A Case Report.
Boudina M, Zisimopoulou E, Rakitzi P, Barbanis S, Syndouka E, Zouli C, Fotiadou A, Stamati MS, Balodimou C, Christantoniou G, Chrisoulidou A. Boudina M, et al. Among authors: fotiadou a. Int Med Case Rep J. 2024 Feb 26;17:143-147. doi: 10.2147/IMCRJ.S437191. eCollection 2024. Int Med Case Rep J. 2024. PMID: 38435418 Free PMC article.
"How Do Greeks Sleep?" A Cross-Sectional Study among Indigenous and Minority Populations.
Georgiadi K, Tsiptsios D, Fotiadou A, Kaltsatou A, Vafeiadis I, Lialiaris S, Trypsiani I, Kitmeridou S, Karatzetzou S, Manolis A, Tsamakis K, Serdari A, Nena E, Steiropoulos P, Tripsianis G. Georgiadi K, et al. Among authors: fotiadou a. Maedica (Bucur). 2022 Sep;17(3):615-627. doi: 10.26574/maedica.2022.17.3.615. Maedica (Bucur). 2022. PMID: 36540581 Free PMC article.
66 results