Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Georgia Ntali"'
Publikováno v:
Medicina, Vol 60, Iss 8, p 1241 (2024)
Cardiovascular comorbidities owing to hormonal excess or deficiency are the main cause of mortality in patients with pituitary disorders. In patients with Cushing’s Disease, there is an increased prevalence of cardiovascular diseases and/or risk fa
Externí odkaz:
https://doaj.org/article/ea04f30d83524c6d8211762c52e66d73
Autor:
Georgia Ntali, Cristina Capatina
Publikováno v:
Medicina, Vol 58, Iss 8, p 1071 (2022)
Functioning gonadotroph adenomas (FGAs) are rare tumors, as the overwhelming majority of gonadotroph tumors are clinically silent. Literature is based on case reports and small case series. Gonadotroph tumors are poorly differentiated and produce and
Externí odkaz:
https://doaj.org/article/285bd38174e040b0948075e7182fa8ff
Autor:
Georgia Ntali, Niki Karavitaki
Publikováno v:
F1000Research, Vol 4 (2015)
Acromegaly is a rare condition of GH excess associated with significant morbidities (e.g. hypertension, glucose intolerance or diabetes mellitus, cardiac, cerebrovascular, respiratory disease and arthritis) and, when uncontrolled, high mortality. Sur
Externí odkaz:
https://doaj.org/article/94b7fbb3dab54ba0a8c2f84b1de7fee4
Publikováno v:
Endocrine Abstracts.
Autor:
Chrysoula Koukoula, Olga Papalou, Aristidis Diamantopoulos, Aikaterini Beka, Dimitra Baikousi, Vasiliki Antonopoulou, Georgia Ntali, Theodora Stratigou, Phoebe Rontogianni, Ioannis Datseris, Dimitra Vassiliadi, Stylianos Tsagarakis
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Faculty Reviews. 12
Autor:
Aikaterini Lavrentaki, Georgia Ntali
Publikováno v:
Handbook of Cancer and Immunology ISBN: 9783030809621
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee669cdb8ea03901dbdef4d69128dc97
https://doi.org/10.1007/978-3-030-80962-1_172-1
https://doi.org/10.1007/978-3-030-80962-1_172-1
Autor:
Efstratios Kardalas, Georgia Ntali, Panagiotis Mouchtouris, Aglaia Papachristou, Aikaterini Lavrentaki, Stylianos Tsagarakis
Publikováno v:
Endocrine Abstracts.
Autor:
Athanasios Fountas, Georgia Kanti, Spyridoula Glycofridi, Maria A. Christou, Athanasia Kalantzi, Irene Giagourta, Athina Markou, Georgia Ntali, Chrysanthi Aggeli, Eleftheria Saoulidou, Antonia Dimakopoulou, George N. Zografos, Theodora Kounadi, Stelios Tigas, Labrini Papanastasiou
Publikováno v:
Endocrine. 78(3)
Pheochromocytomas are rare tumors and biochemically silent ones with normal catecholamine levels are even rarer. Up to date, biochemically inactive pheochromocytomas are poorly investigated. We aimed to systematically assess the pre- and peri-operati
Publikováno v:
Endocrine. 73:16-30
Females with NC21OHD may present as asymptomatic or develop a wide range of androgen excess expression. Clinical manifestations may become evident in childhood and adolescence and include premature pubarche, precocious puberty, acne, hirsutism, and m