Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Eirini Dikaiakou"'
Autor:
Eirini Dikaiakou, Fani Athanasouli, Anatoli Fotiadou, Maria Kafetzi, Stefanos Fakiolas, Stefanos Michalacos, Elpis Athina Vlachopapadopoulou
Publikováno v:
Metabolites, Vol 13, Iss 2, p 230 (2023)
The hypertriglyceridemic waist (HTGW) phenotype is characterized by abdominal obesity and elevated serum triglycerides. We aimed to assess the prevalence of the HTGW phenotype among children with overweight or obesity and its association with indices
Externí odkaz:
https://doaj.org/article/b7eb35e740114466b4b32deeb1d7ca95
Autor:
Myrto Bonataki, Eirini Dikaiakou, Panagiota Anastasopoulou, Stefanos Fakiolas, Maria Kafetzi, Elpis Athina Vlachopapadopoulou
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 36:508-512
Objectives Autoimmune polyglandular syndrome type 2 (APS2) is characterized by autoimmune adrenal insufficiency (AI) in conjunction with autoimmune thyroid disease (AITD) and/or type 1 diabetes mellitus (T1DM). The aim is to report an 11-year-old gir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e23ece6fb903012cd1b6ef019818ab4c
https://doi.org/10.1515/jpem-2022-0619
https://doi.org/10.1515/jpem-2022-0619
Autor:
Elpis-Athina Vlachopapadopoulou, Eirini Dikaiakou, Stefanos Michalacos, Elizabeth Barbara Tatsi, Popi Sifianou, Amalia Sertedaki, Christina Kanaka-Gantenbein, Anatoli Fotiadou
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:527-530
Objectives Congenital Hyperinsulinism (CHI) is the most common cause of persistent hypoketotic hypoglycaemia in neonates and infants. It is a genetic disorder with both familial and sporadic forms. Case Presentation In this study, we examined two unr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b128701d0050151b697df52955cce32f
https://doi.org/10.1515/jpem-2020-0302
https://doi.org/10.1515/jpem-2020-0302
Autor:
Maria Kafetzi, Eirini Dikaiakou, Elpis Vlachopapadopoulou, Stefanos Michalacos, Fani Athanasouli, Elli Anagnostou, Aspasia Fotinou, Ioanna Patinioti
Publikováno v:
Journal of Obesity and Chronic Diseases. 4:6-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::346adac9a6d22a2e5574060a12534db2
https://doi.org/10.17756/jocd.2020-032
https://doi.org/10.17756/jocd.2020-032
Autor:
Marina Vakaki, Anatoli Fotiadou, Stefanos Michalacos, Fani Athanasouli, Elpis Vlachoapapadopoulou, Lina Michala, Eirini Dikaiakou, Martha Moisidou
Publikováno v:
Developmental and Adolescent Health.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff4988594b72a0e1588428a672789d8b
https://doi.org/10.54088/0er03
https://doi.org/10.54088/0er03
Autor:
Maria Kafetzi, Vasilios Petrou, Dimitra Tampouratzi, Elpis Vlachopapadopoulou, Fani Athanasouli, Eirini Dikaiakou, Stefanos Michalakos, Leka-Emiri Sofia
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3995e8bfd670ba1cc4a662d213ac1c40
https://doi.org/10.1530/endoabs.73.pep3.6
https://doi.org/10.1530/endoabs.73.pep3.6
Autor:
Agnès Linglart, Kyriaki Karavanaki, Patrick Hanna, Maria Tsolia, Stefanos Michalacos, Elli Anagnostou, Eirini Dikaiakou, Elpis-Athina Vlachopapadopoulou
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 33(11)
Objectives The objective of this paper is to report a peculiar case of a patient with pseudohypoparathyroidism type 1b (PHP1B). Pseudohypoparathyroidism (PHP) refers to a group of disorders characterized by hypocalcemia, hyperphosphatemia, and elevat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec60da159e956e5d75d3b49d151ca48d
https://pubmed.ncbi.nlm.nih.gov/33027051
https://pubmed.ncbi.nlm.nih.gov/33027051
Autor:
Elpis Vlachopapadopoulou, Emannouil Manolakos, Eirini Dikaiakou, Stefanos Michalacos, Ioannis Papoulidis, Ioannis Panagiotopoulos
Publikováno v:
Journal of the Endocrine Society
Background: Chromosomal deletions may lead to variable phenotypic alterations, depending on which loci and genes are deleted. We present the case of a boy with a de novo 1p13.2 deletion which was diagnosed by array-CGH analysis. Clinical Case: A Gree
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b21c69b9e7d003ccad195963d59d43ac
https://doi.org/10.1210/jendso/bvaa046.731
https://doi.org/10.1210/jendso/bvaa046.731
Autor:
Eirini Dikaiakou, Maria Kafetzi, Elpis Vlachopapadopoulou, Fani Athanasouli, Stavroula A Paschou, Ιoannis Panagiotopoulos, Aspasia Fotinou, Stephanos Michalacos
Publikováno v:
Endocrine. 70(1)
To investigate the association between Triglyceride-glucose (TyG) index and the Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) and Matsuda indices in Greek obese children and adolescents, in order to assess whether it could be used as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f930090e7cad7b63157d22201381505b
https://pubmed.ncbi.nlm.nih.gov/32770305
https://pubmed.ncbi.nlm.nih.gov/32770305
Autor:
Panagiotis Samelis, Christos Zampakides, Rodanthi Margariti, Elpis Vlachopapadopoulou, Stefanos Michalacos, Emanouil Manolakos, Eirini Dikaiakou
Publikováno v:
Molecular Syndromology. 9:241-246
A boy and his father with severe short stature, progressively evolving body asymmetry, and skeletal abnormalities are presented. A next-generation sequencing exome study was performed, and the patient was found heterozygous for the c.1609G>A (p.Gly53
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::346f3e15d61afe848a06fbab4c9d009b
https://doi.org/10.1159/000492190
https://doi.org/10.1159/000492190