Zobrazeno 1 - 10
of 157
pro vyhledávání: '"G Piaditis"'
Autor:
K. Alexandraki, P. Makras, A. Protogerou, A. Stathopoulou, K. Dimitriou, D. Papadogias, E. Voidonikola, G. Piaditis, C. Papamichael, G. Kaltsas
Publikováno v:
Artery Research, Vol 1, Iss 1 (2007)
Externí odkaz:
https://doaj.org/article/e339413965b8471b971713fbaf0d3564
Publikováno v:
Expert review of endocrinologymetabolism. 2(6)
Langerhans’ cell histiocytosis (LCH) is a rare disease of unknown etiology and variable biologic behavior and course. Almost every organ can be affected; however, it frequently involves the bones, lungs, skin and lymph nodes. LCH exhibits a particu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39fdd104ff569e86f1863e1c2654d2bf
https://pubmed.ncbi.nlm.nih.gov/30290476
https://pubmed.ncbi.nlm.nih.gov/30290476
Autor:
Lina Papanastasiou, Gregory Kaltsas, Aparna Pal, Carolina Cohen, Marina Tsoli, Soledad Sosa, Karina Danilowicz, Ashley B. Grossman, G. Piaditis, Anna Angelousi
Publikováno v:
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme. 50(4)
Primary hypophysitis (PH) is a rare disease with a poorly-defined natural history. Our aim was to characterise patients with PH at presentation and during prolonged follow-up. Observational retrospective study of 22 patients was conducted from 3 cent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e070528e647353b4c738eb2898962bab
https://pubmed.ncbi.nlm.nih.gov/29458219
https://pubmed.ncbi.nlm.nih.gov/29458219
Autor:
Dimitra Vassiliadi, Marinella Tzanela, G. Piaditis, N. Mazarakis, V. Tsatlidis, E. Margelou, Stylianos Tsagarakis, M. Tampourlou
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 100:3478-3485
The bilateral formation of nodules indicates that the pathogenesis of bilateral adrenal incidentalomas (AI) may differ from that of unilateral AI. A possible role of hypothalamo-pituitary-adrenal (HPA) axis dysregulation in their formation has not be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4791319822c01c98a92a021ef21d2694
https://doi.org/10.1210/jc.2015-1653
https://doi.org/10.1210/jc.2015-1653
Autor:
Gregory Kaltsas, Christianna Samara, Kita M, L. Papanastasiou, Tsolakidou K, Anastasiou A, Krystallenia I Alexandraki, Alexandra Chrisoulidou, G. Piaditis
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 122:15-19
With the advent of modern imaging modalities, endocrine incidentalomas are increasingly being discovered. We aimed to investigate the presence of pituitary incidentalomas (PI) in patients with adrenal incidentalomas (AI), and identify potential metab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::decd6a4038c1f24f3efd72b96a783a45
https://doi.org/10.1055/s-0033-1358761
https://doi.org/10.1055/s-0033-1358761
Background: Germline mutations of the KCNJ5 gene encoding Kir3·4, a member of the inwardly rectifying K+ channel, have been identified in ‘normal’ adrenal glands, patients with familial hyperaldosteronism (FH) type III, aldosterone-producing ade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a0f79becf3229a55c57c9f9fea7850cb
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086465
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086465
Autor:
Gregory Kaltsas, Athina Markou, Ioannis I. Androulakis, G. Piaditis, Aggeliki Gouli, George P. Chrousos, Georgios Zografos, Kyriakos Vamvakidis, Despina Ragkou, G. Kontogeorgos, Anastasia Tzonou
Publikováno v:
European Journal of Clinical Investigation. 41:1227-1236
Eur J Clin Invest 2011; 41 (11): 1227–1236 Abstract Background Previous studies based on standard endocrine testing have generally shown a low prevalence of primary aldosteronism, a form of autonomous aldosterone secretion (AAS), in hypertensive in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f59ef0a2561fa6bb3c7dce5426b41772
https://doi.org/10.1111/j.1365-2362.2011.02531.x
https://doi.org/10.1111/j.1365-2362.2011.02531.x
Akademický článek
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Autor:
A.B. Grossman, C.M. Papamichael, G. Piaditis, A.D. Protogerou, P. Voidonikola, Krystallenia I Alexandraki, K. Dimitriou, Anastassios G. Pittas, Gregory Kaltsas, Dimitris Papadogias, Polyzois Makras, A. Stathopoulou
Publikováno v:
QJM. 101:31-40
Background: Langerhans-cell histiocytosis (LCH) is a rare disease with features of chronic inflammation and it may also induce hypopituitarism, conditions associated with an increased risk of cardiovascular diseases. Aim: Cardiovascular and metabolic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62bff883b2898cb947d6942c09575729
https://doi.org/10.1093/qjmed/hcm118
https://doi.org/10.1093/qjmed/hcm118
Autor:
Dimitris Papadogias, A. Zetos, Evangelos Andreakos, Gregory Kaltsas, Z. Nikolakopoulou, G. Kontogeorgos, G. Piaditis, Polyzois Makras, Georgios Toloumis, Christianna Samara, M. Antoniou
Publikováno v:
Neuroradiology. 48:37-44
Langerhans cell histiocytosis (LCH) is a rare, systemic disease caused by monoclonal expansion of dendritic cells that shows a particular predilection for the hypothalamic-pituitary system (HPS). We studied the function (anterior and posterior pituit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::992eb1a2adb8de7a19de8d5905b13e78
https://doi.org/10.1007/s00234-005-0011-x
https://doi.org/10.1007/s00234-005-0011-x