Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Michalis Picolos"'
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
Autor:
Pavlos Fanis, Nicos Skordis, Meropi Toumba, Michalis Picolos, George A. Tanteles, Vassos Neocleous, Leonidas A. Phylactou
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveThe study aimed to identify the pathogenic status of p.Gln319Ter (NM_000500.7: c.955C>T) variant when inherited in a single CYP21A2 gene (bimodular RCCX haplotype) and to discriminate between a non-causing congenital adrenal hyperplasia (CAH
Externí odkaz:
https://doaj.org/article/a1eec0745c8d402093048b3fcf3512cb
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
Autor:
Vassos Neocleous, Pavlos Fanis, Meropi Toumba, Alexia A. P. Phedonos, Michalis Picolos, Elena Andreou, Tassos C. Kyriakides, George A. Tanteles, Christos Shammas, Leonidas A. Phylactou, Nicos Skordis
Publikováno v:
International Journal of Endocrinology, Vol 2017 (2017)
Heterozygosity for CYP21A2 mutations 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
Externí odkaz:
https://doaj.org/article/a06836efd0164039ab1a9291f37ebb7a
Autor:
Angelos Kyriacou, Akheel A. Syed, Nadia Sawicka‐Gutaj, Michalis Picolos, Panayiotis Economides, Alexis Kyriacou
Publikováno v:
Kyriacou, A, Syed, A A, Sawicka-Gutaj, N, Picolos, M, Economides, P & Kyriacou, A 2022, ' Body weight change trajectories following the treatment of hyperthyroidism : a prospective cohort study ', Clinical Endocrinology . https://doi.org/10.1111/cen.14873
Hyperthyroidism is a well-recognised cause of significant metabolic changes with most patients experiencing weight loss in the acute illness This article is protected by copyright. All rights reserved.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::497bced6296fd11743dbd51b2cf99203
https://doi.org/10.1111/cen.14873
https://doi.org/10.1111/cen.14873
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
https://pubmed.ncbi.nlm.nih.gov/36215117
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
https://doi.org/10.1055/a-0957-3297
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
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
https://doi.org/10.1155/2017/8984365
Autor:
Nicos Skordis, Demetrios Monos, Paul Costeas, Michalis Picolos, Vicky Nicolaidou, Petroula Gerasimou
Publikováno v:
PLoS ONE
PLoS ONE, Vol 13, Iss 3, p e0193684 (2018)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d94428191f8048bc036d203a7cc9e08
http://europepmc.org/articles/PMC5832312
http://europepmc.org/articles/PMC5832312