Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Artemis Doulgeraki"'
Autor:
Charalampos Tsentidis, Dimitrios Gourgiotis, Lydia Kossiva, Antonios Marmarinos, Artemis Doulgeraki, Kyriaki Karavanaki
Publikováno v:
Endocrines, Vol 4, Iss 4, Pp 709-719 (2023)
Background: Diabetes mellitus is an increasing global health emergency, with serious complications (including osteoporosis). Leptin and adiponectin are among the least-investigated possible contributing factors of T1D low bone mass. Methods: In this
Externí odkaz:
https://doaj.org/article/ad356f17b97c4d778946c7daf47d23f8
Autor:
Artemis Doulgeraki, Michaël R. Laurent
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/a75c5a50811b493990eca25b9f45ecd4
Autor:
Artemis Doulgeraki, Laura Bani-Odeh, Despina Tramma, Georgios Giataganas, Fotis Kirvassilis, Konstantinos Kollios, Maria Fotoulaki
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism.
Osteopetrorickets is a rare complication of autosomal recessive (“malignant”) osteopetrosis. Its prompt diagnosis is essential, because early suspicion of infantile osteopetrosis enables treatment with human stem cell transplantation, depending o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e43a767bf9765c3b31fdf99b31d20de5
https://doi.org/10.1515/jpem-2023-0001
https://doi.org/10.1515/jpem-2023-0001
Autor:
Sofia Leka-Emiri, Adamantios Katerelos, Konstantinos A. Voudris, Artemis Doulgeraki, Emmanouil Manolakos, Anastasia Korona, Ioannis Papoulidis, Sotiria Mastroyanni, Athina Ververi, Stella Mouskou, Georgios Vartzelis
Publikováno v:
Molecular Syndromology. 12:194-200
Snyder-Robinson syndrome (SRS) is an extremely rare X-linked intellectual disability syndrome (MRXSSR; MIM #309583). The main clinical features of SRS include psychomotor delay, hypotonia, and asthenic-type body habitus – reduced body weight and bo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7b594aa4c2171b710c2960dd9fd05af
https://doi.org/10.1159/000514122
https://doi.org/10.1159/000514122
Autor:
Tania Siahanidou, Christina Kanaka‑Gantenbein, Flora Bacopoulou, George P. Chrousos, Artemis Doulgeraki, Arsinoi Koutroumpa, Helen Bouza, Aimilia Mantzou
Publikováno v:
Hormone Research in Paediatrics. 94:416-425
Introduction: Prematurity is associated with increased cardiometabolic risk later in life. The adipomyokine irisin has been acknowledged as a modulator of energy metabolism and insulin sensitivity. The aim of this study was to investigate circulating
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d25d1df57a48e04497a592a315b668be
https://doi.org/10.1159/000521265
https://doi.org/10.1159/000521265
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 5676, p 5676 (2021)
Journal of Clinical Medicine
Journal of Clinical Medicine
Hypophosphatasia (HPP) is an inherited metabolic disease caused by loss-of-function mutations in the tissue non-specific alkaline phosphatase (TNAP) gene. Reduced activity of TNAP leads to the accumulation of its substrates, mainly inorganic pyrophos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df31ec87c7ad69af9d01aa1f2e9972ef
https://www.mdpi.com/2077-0383/10/23/5676
https://www.mdpi.com/2077-0383/10/23/5676
Autor:
Artemis Doulgeraki, Vasiliki Schiza, Kalliopi Drakaki, Jacqueline Yousef, Helen Athanasopoulou, Christine Fragodimitri, Fotis Karabatsos, Ioannis Monopolis, Antonia Chatziliami
Publikováno v:
Hemoglobin. 45(1)
Hereditary hemolytic disorders cause ineffective erythropoiesis and bone marrow hyperplasia. Little is known about their effect on growth and skeletal health. The aim of this study was to evaluate growth, bone and body composition of non transfusion-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad7fb7d6683c02277bd7ea03cc9cc43b
https://pubmed.ncbi.nlm.nih.gov/33557624
https://pubmed.ncbi.nlm.nih.gov/33557624
Autor:
Lydia Kossiva, Kyriaki Karavanaki, Charalampos Tsentidis, George Polyzois, Christina Kanaka-Gantenbein, Margarita Baka, Helen Athanasopoulou, Maria Nikita, Artemis Doulgeraki, Marina Servitzogloy
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b549821f02c913a8acc0db7a256b51e9
https://doi.org/10.1530/endoabs.70.aep125
https://doi.org/10.1530/endoabs.70.aep125
Autor:
Michail Sarantis, Artemis Doulgeraki, Yolanda Gyftodimou, Panagoula Kollia, Evdoxia Mpourazani, Stavroula Samara, Helen Athanasopoulou, Dimitra Lianou
Publikováno v:
Journal of Research and Practice on the Musculoskeletal System. :75-80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a4f1bca004e0980524333049bb84558
https://doi.org/10.22540/jrpms-02-075
https://doi.org/10.22540/jrpms-02-075
Autor:
Artemis Doulgeraki, Anders Kämpe, Panagiotis Ν Krallis, Outi Mäkitie, Emmanouil M Karavitakis, Alice Costantini, Fulya Taylan
Publikováno v:
Journal of Human Genetics. 63:923-926
Mutations in the gene encoding plastin-3, PLS3, have recently been associated to severe primary osteoporosis. The molecular function of plastin-3 is not fully understood. Since PLS3 is located on the X chromosome, males are usually more severely affe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42714f6a06a67026b65dd556884485b
https://doi.org/10.1038/s10038-018-0472-5
https://doi.org/10.1038/s10038-018-0472-5