Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Konstantina Kosta"'
Autor:
Pelagia Tsakona, Vaios Dafoulis, Anastasios Vamvakis, Konstantina Kosta, Styliani Mina, Ioannis Kitsatis, Alexandra Hristara-Papadopoulou, Emmanuel Roilides, Kyriaki Tsiroukidou
Publikováno v:
Children, Vol 8, Iss 6, p 443 (2021)
Type 1 diabetes mellitus (T1DM) is a chronic disease that can affect the physical and mental health of children and adolescents, often leading to anxiety disorders with chronic activation of the hypothalamic axis (HPA). Moreover, a great proportion o
Externí odkaz:
https://doaj.org/article/1335d45ca9314952848dd8029673e4c1
Autor:
Emmanouil Roilides, Georgios Tsikopoulos, Pavlos Fanis, Vassos Neocleous, Leonidas A. Phylactou, Konstantina Kosta, Stefan A. Wudy, Michaela F. Hartmann, Aristea Karipiadou, Nicos Skordis, Nikolaos Karantaglis, Dimitrios T Papadimitriou, Maria Papagianni
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 34:131-136
Objectives 3β-Hydroxysteroid dehydrogenase (3β-HSD) deficiency is a rare type of congenital adrenal hyperplasia caused by recessive loss-of-function mutations in HSD3B2 gene. Case presentation We report an 8.5-year-old, 46XY, Roma boy with advanced
Autor:
Christos Chatzakis, George Mastorakos, Kyriaki Tsiroukidou, Ioannis Tsanakas, Dimitrios Floros, Maria Papagianni, Konstantina Kosta, Anastasios Vamvakis, E. Hatziagorou, Nikolaos Koletsos
Publikováno v:
Diabetes Technology & Therapeutics. 21:627-634
Background: Euglyca® is a mobile application which we developed for children and adolescents suffering type 1 diabetes mellitus (T1DM) for calculation of the appropriate insulin bolus dose...
Autor:
Vaios Dafoulis, Emmanuel Roilides, Pelagia Tsakona, Ioannis Kitsatis, Alexandra Hristara-Papadopoulou, Styliani Mina, Anastasios Vamvakis, Konstantina Kosta, Kyriaki Tsiroukidou
Publikováno v:
Children
Children, Vol 8, Iss 443, p 443 (2021)
Children, Vol 8, Iss 443, p 443 (2021)
Type 1 diabetes mellitus (T1DM) is a chronic disease that can affect the physical and mental health of children and adolescents, often leading to anxiety disorders with chronic activation of the hypothalamic axis (HPA). Moreover, a great proportion o
Autor:
John Tsanakas, Kiriaki Tsiroukidou, E. Hatziagorou, Maria Papagianni, Kalliopi Kontouli, Asterios Kampouras, Konstantina Kosta
Publikováno v:
7.1 Paediatric Respiratory Physiology and Sleep.
INTRODUCTION: Leptin has been identified as a key hormone in weight and energy homeostasis both in children and adults. AIM: To examine whether adipokines (leptin, adiponektin) along with resistance to insulin index (Homa-IR) can be related independe
Autor:
Maria Papagianni, Kiriaki Tsiroukidou, Kiriaki Papa, Maria Kiriakou, Elena Laskaridou, Anastasios Vamvakis, Ioannis Ttsanakas, Iliana Mameka, Konstantina Kosta
Publikováno v:
Clinical Nutrition ESPEN. 24:188
Autor:
Kyriaki Tsiroukidou, Konstantina Kosta, Christos Sampanis, Maria Papagianni, Theodora Griva, Ioanna Zografou, Athena Pyrpasopoulou, Panagiota Karagianni, Anastasios Vamvakis
Publikováno v:
Endocrine Abstracts.
Autor:
Nikolaos P.E. Kadoglou, Kiriaki Tsiroukidou, Konstantina Kosta, Maria Papadopoulou, Maria Papagianni, Konstantinos Kitsios
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: To compare high-sensitivity C-reactive protein (hsCRP) levels in obese and overweight children and adolescents to normal-weight individuals as well as to compare hsCRP levels in overweight children/adolescents with and without additional m
Autor:
Ian Sabroe, M. Dawn Teare, Konstantina Kosta, John Tsanakas, Jonathan Göke, Moira K. B. Whyte, Robert J.D. Nibbs
Publikováno v:
American journal of human genetics. 81(4)
Segmental copy-number polymorphisms (CNPs) represent a significant component of human genetic variation and are likely to contribute to disease susceptibility. These potentially multiallelic and highly polymorphic systems present new challenges to fa
Publikováno v:
Hormones (Athens, Greece). 5(3)
The McCune-Albright Syndrome (MAS) is a sporadic rare disease first described in 1936 by McCune and separately by Albright. MAS is characterized by a triad of physical signs: cafe-au-lait spots, polyostotic fibrous dysplasia and autonomous endocrine