Real-world application of ATA Guidelines in over 600 aspirated thyroid nodules: is it time to change the size cut-offs for FNA?

Autor: Stamatina Ioakim, Akheel A Syed, George Zavros, Michalis Picolos, Luca Persani, Angelos Kyriacou

Publikováno v: European Thyroid Journal, Vol 11, Iss 6, Pp 1-10 (2023)

Background: The 2015 American Thyroid Association (ATA) Guidelines recommend the following size cut-offs based on sonographic appearances for subjecting nodules to fine-needle aspiration (FNA) biopsy: low risk: 15 mm and inte rmediate risk and high r

Externí odkaz: https://doaj.org/article/0f200e94694f4821b3a2edafced8d9f2

Combined effect of glutamine at position 70 of HLA-DRB1 and alanine at position 57 of HLA-DQB1 in type 1 diabetes: An epitope analysis.

Autor: Petroula Gerasimou, Vicky Nicolaidou, Nicos Skordis, Michalis Picolos, Demetrios Monos, Paul A Costeas

Publikováno v: PLoS ONE, Vol 13, Iss 3, p e0193684 (2018)

The contribution of specific HLA Class II alleles in type 1 diabetes is determined by polymorphic amino acid epitopes that direct antigen binding therefore, along with conventional allele frequency analysis, epitope analysis can provide important ins

Externí odkaz: https://doaj.org/article/22d903e40694491882b1c9167d023f43

Real-world application of ATA Guidelines in over 600 aspirated thyroid nodules: is it time to change the size cut-offs for FNA?

Autor: Stamatina Ioakim, Akheel A Syed, George Zavros, Michalis Picolos, Luca Persani, Angelos Kyriacou

Publikováno v: Ioakim, S, Syed, A A, Zavros, G, Picolos, M, Persani, L & Kyriacou, A 2022, ' Real world application of ATA guidelines in over 600 aspirated thyroid nodules : is it time to change the size cut-offs for FNA? ', European thyroid journal, vol. 11, no. 6 . https://doi.org/10.1530/ETJ-22-0163

Background The 2015 American Thyroid Association (ATA) Guidelines recommend the following size cut-offs based on sonographic appearances for subjecting nodules to fine-needle aspiration (FNA) biopsy: low risk: 15 mm and intermediate risk and high ris

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4469c29122724c093a7ccc0cd6770bb5
https://pubmed.ncbi.nlm.nih.gov/36215117

The Spectrum of Genetic Defects in Congenital Adrenal Hyperplasia in the Population of Cyprus: A Retrospective Analysis

Autor: Vassos Neocleous, Elena Andreou, Meropi Toumba, Stella Nicolaou, Charilaos Stylianou, George A. Tanteles, Nicos Skordis, Michalis Picolos, Pavlos Fanis, Michalis Iasonides, Andreas Kyriakou, Tassos C. Kyriakides, Leonidas A. Phylactou

Publikováno v: Hormone and Metabolic Research

Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) is caused by mutations in the CYP21A2 gene. The study refers to CAH patients of Greek-Cypriot ancestry between years 2007 and 2018. One hundred and twenty patients with va

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa09bce5205e486dcfeed5b5c35f466b
https://doi.org/10.1055/a-0957-3297

Variations in the 3′UTR of theCYP21A2Gene in Heterozygous Females with Hyperandrogenaemia

Autor: Pavlos Fanis, Nicos Skordis, Alexia A P Phedonos, Vassos Neocleous, Tassos C. Kyriakides, Meropi Toumba, Leonidas A. Phylactou, George A. Tanteles, Christos Shammas, Elena Andreou, Michalis Picolos

Publikováno v: International Journal of Endocrinology, Vol 2017 (2017)
International Journal of Endocrinology

Heterozygosity forCYP21A2mutations in females is possibly related to increased risk of developing clinical hyperandrogenism. The present study was designed to seek evidence on the phenotype-genotype correlation in female children, adolescents, and wo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf8b604f1216b6e9eeb952fa928f87f2
https://doi.org/10.1155/2017/8984365