Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Frederick, Anthony"'
Publikováno v:
Endocrine Regulations, Vol 53, Iss 3, Pp 191-212 (2019)
Pheochromocytomas are rare tumors originating in the adrenal medulla. They may be sporadic or in the context of a hereditary syndrome. A considerable number of pheochromocytomas carry germline or somatic gene mutations, which are inherited in the aut
Externí odkaz:
https://doaj.org/article/0732cad180d4417c8701aa79527cbde5
Autor:
Farrugia Frederick-Anthony, Zavras Nicolaos, Martikos Georgios, Tzanetis Panagiotis, Charalampopoulos Anestis, Misiakos Evangelos P., Sotiropoulos Dimitrios, Koliakos Nikolaos
Publikováno v:
Endocrine Regulations, Vol 52, Iss 1, Pp 27-40 (2018)
Objectives. The aim of this study was to present up to date information concerning the diagnosis and treatment of primary aldosteronism (PA). PA is the most common cause of endocrine hypertension. It has been reported up to 24% of selective referred
Externí odkaz:
https://doaj.org/article/72038cff5ae84d06866918d16555abab
Autor:
Farrugia Frederick-Anthony, Misiakos Evangelos, Martikos Georgios, Tzanetis Panagiotis, Charalampopoulos Anestis, Zavras Nicolaos, Sotiropoulos Dimitrios, Koliakos Nikolaos
Publikováno v:
Romanian Journal of Internal Medicine, Vol 55, Iss 4, Pp 188-197 (2017)
Objectives. To present a step by step approach for the diagnosis of adrenal incidentaloma (AI).
Externí odkaz:
https://doaj.org/article/bcaed13a1a5f475084dc6b398b934c24
Publikováno v:
ARKIVOC, Vol 2017, Iss 1, Pp 117-147 (2017)
Externí odkaz:
https://doaj.org/article/62e3a7d7120947e9974ea58dd4c25b72
Autor:
Frederick Anthony Wilkinson
This collection of short stories and vignettes is at once sad, humorous, and inspiring, set against the backdrop of the Diaspora. Woven from the recollections and experiences of childhood in a society divided by religion, expectations, despair, and h
Autor:
Nikolaos Koliakos, Frederick Anthony Farrugia, Nikolaos Zavras, Vasileios C. Kollaras, Dimitrios C. Papakonstantinou, Kostantinos G. Kopanakis, Anestis Charalampopoulos
Publikováno v:
Chirurgia. 32
Publikováno v:
Endocrine Regulations, Vol 53, Iss 3, Pp 191-212 (2019)
Pheochromocytomas are rare tumors originating in the adrenal medulla. They may be sporadic or in the context of a hereditary syndrome. A considerable number of pheochromocytomas carry germline or somatic gene mutations, which are inherited in the aut
Autor:
Nikolaos Koliakos, Dimitrios Sotiropoulos, Frederick-Anthony Farrugia, Evangelos P. Misiakos, Georgios Martikos, Anestis Charalampopoulos, Nicolaos Zavras, Panagiotis Tzanetis
Publikováno v:
Romanian Journal of Internal Medicine, Vol 55, Iss 4, Pp 188-197 (2017)
Objectives. To present a step by step approach for the diagnosis of adrenal incidentaloma (AI).Method. An extensive review of the literature was conducted, searching the Pub-Med and Google Scholar using the Mesh terms; Adrenal; Incidentaloma; Adrenal
Autor:
Nicolaos Zavras, Panagiotis Tzanetis, Dimitrios Sotiropoulos, Frederick-Anthony Farrugia, Anestis Charalampopoulos, Georgios Martikos, Evangelos P. Misiakos
Publikováno v:
Endocrine Regulations, Vol 51, Iss 3, Pp 168-181 (2017)
Objective. We conducted an extensive review of the literature and tried to cite the most recent recommendations concerning the pheochromocytoma (PHEO). Methods. Pub Med and Google Scholar databases were searched systematically for studies concerning