Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Styliani Giza"'
Autor:
Eleni P. Kotanidou, Vasiliki Rengina Tsinopoulou, Styliani Giza, Stergianna Ntouma, Chrysanthi Angeli, Michail Chatziandreou, Konstantinos Tsopelas, Ioulia Tseti, Assimina Galli-Tsinopoulou
Publikováno v:
Children, Vol 10, Iss 11, p 1814 (2023)
Global rates of adolescent obesity have led the World Health Organization to consider the disease a pandemic that needs focus. In search of new anti-obesity agents, Crocus sativus, popularly known as saffron, is a nutraceutical agent, praised for its
Externí odkaz:
https://doaj.org/article/b1144e06a9a44baba81aed94fc5f2dd1
Autor:
Anastasios Serbis, Vasiliki Rengina Tsinopoulou, Anastasia Papadopoulou, Savvas Kolanis, Eleni I. Sakellari, Kosmas Margaritis, Eleni Litou, Stergianna Ntouma, Styliani Giza, Eleni P. Kotanidou, Assimina Galli-Tsinopoulou
Publikováno v:
Diagnostics, Vol 13, Iss 9, p 1588 (2023)
Despite being classified as benign tumors, craniopharyngiomas (CPs) are associated with significant morbidity and mortality due to their location, growth pattern, and tendency to recur. Two types can be identified depending on age distribution, morph
Externí odkaz:
https://doaj.org/article/7dbff76ff3aa4b1bba814aac351660ac
Autor:
Eleni P Kotanidou, Styliani Giza, Vasiliki Rengina Tsinopoulou, Kosmas Margaritis, Anastasia Papadopoulou, Eleni Sakellari, Savvas Kolanis, Eleni Litou, Anastasios Serbis, Assimina Galli-Tsinopoulou
Publikováno v:
Diagnostics, Vol 13, Iss 6, p 1187 (2023)
Thyroid cancer represents the prominent endocrine cancer in children. Papillary thyroid cancer (PTC) constitutes its most frequent (>90%) pediatric histological type. Mutations energizing the mitogen-activated-protein kinase (MAPK) pathway are defini
Externí odkaz:
https://doaj.org/article/690b5de812ff47b8b236a73908d6e65c
Autor:
Anastasios Serbis, Vassiliki Regina Tsinopoulou, Konstantina Mouzaki, Eleni P. Kotanidou, Styliani Giza, Assimina Galli-Tsinopoulou
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 23, Iss 3, Pp 162-165 (2018)
X-linked adrenal hypoplasia congenita (AHC) is a rare disorder that usually presents clinically as adrenal insufficiency in early infancy. It is caused by mutations in the NR0B1 gene which is located on the short arm of chromosome X (Xp21). The NR0B1
Externí odkaz:
https://doaj.org/article/1593b4f5eca046b88041ca0c9cd501c8
Autor:
Kosmas Margaritis, Georgia Margioula-Siarkou, Styliani Giza, Eleni P. Kotanidou, Vasiliki Regina Tsinopoulou, Athanasios Christoforidis, Assimina Galli-Tsinopoulou
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 22, p 12165 (2021)
Type-1 diabetes mellitus (T1DM) is one of the most well-defined and complex metabolic disorders, characterized by hyperglycemia, with a constantly increasing incidence in children and adolescents. While current knowledge regarding the molecules relat
Externí odkaz:
https://doaj.org/article/303f338fd9ff49a8be69d072cfb8a551
Autor:
Assimina Galli-Tsinopoulou, Eleni P Kotanidou, Vasiliki-Regina Tsinopoulou, Styliani Giza, Maria G. Vogiatzi
Publikováno v:
Current Pharmaceutical Design. 26:5591-5608
Hypertension in childhood and adolescence has increased in prevalence. Interest in the disease was raised after the 2017 clinical practice guidelines of the American Academy of Paediatrics on the definition and classification of paediatric hypertensi
Autor:
Styliani Giza, Assimina Galli-Tsinopoulou, Eleni P Kotanidou, Vasiliki Regina Tsinopoulou, Georgia Margioula-Siarkou, Kosmas Margaritis, Athanasios Christoforidis
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 12165, p 12165 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 12165, p 12165 (2021)
Type-1 diabetes mellitus (T1DM) is one of the most well-defined and complex metabolic disorders, characterized by hyperglycemia, with a constantly increasing incidence in children and adolescents. While current knowledge regarding the molecules relat
Autor:
Styliani Giza
Ο σακχαρώδης διαβήτης τύπου 1 (ΣΔ1) είναι η πιο συχνή αυτοάνοση πάθηση της παιδικής ηλικίας. Στην παθοφυσιολογία του εμπλέκεται το γονίδι
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12f257b3195618618511080077195d53
https://doi.org/10.12681/eadd/36903
https://doi.org/10.12681/eadd/36903
Autor:
Styliani Giza, Vasiliki Rengina Tsinopoulou, Konstantina Mouzaki, Assimina Galli‑Τsinopoulou, Aikaterini Fragou, Anastasios Serbis, Ioannis Kyrgios, Angeliki Kleisarchaki, Eleni P Kotanidou, Georgios Tzimagiorgis
Publikováno v:
Biomed Rep
The insulin (INS) gene is the one of the most important genes involved in the pathogenesis of Type 1 Diabetes (T1D) after the Major Histocompatibility Complex genes. Studies addressing the issue of hyper- or hypo-methylation status of the INS gene pr
Autor:
Assimina Galli-Tsinopoulou, Ioannis Kyrgios, Aikaterini Fragou, Georgios Tzimagiorgis, Styliani Giza
Publikováno v:
Journal of endocrinological investigation. 44(10)
Protein tyrosine phosphatase non-receptor type 22 (PTPN22) is an inhibitor of T-cell activation, regulating intracellular signal transduction and thereby being implicated in the pathogenesis of autoimmune thyroid disease (AITD). The exact molecular m