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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

66 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
SLC2A1 Tag SNPs in Greek Patients with Diabetic Retinopathy and Nephropathy.
Siokas V, Fotiadou A, Dardiotis E, Kotoula MG, Tachmitzi SV, Chatzoulis DZ, Zintzaras E, Stefanidis I, Tsironi EE. Siokas V, et al. Among authors: fotiadou a. Ophthalmic Res. 2019;61(1):26-35. doi: 10.1159/000480241. Epub 2017 Dec 6. Ophthalmic Res. 2019. PMID: 29207384
The contribution of genetic variants of SLC2A1 gene in T2DM and T2DM-nephropathy: association study and meta-analysis.
Stefanidis I, Tziastoudi M, Tsironi EE, Dardiotis E, Tachmitzi SV, Fotiadou A, Pissas G, Kytoudis K, Sounidaki M, Ampatzis G, Mertens PR, Liakopoulos V, Eleftheriadis T, Hadjigeorgiou GM, Santos M, Zintzaras E. Stefanidis I, et al. Among authors: fotiadou a. Ren Fail. 2018 Nov;40(1):561-576. doi: 10.1080/0886022X.2018.1496931. Ren Fail. 2018. PMID: 30353771 Free PMC article.
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.
66 results