Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Dimitrios Papadogias"'
Autor:
Gregory Kaltsas, George Piaditis, Ioannis I. Androulakis, Aggeliki Tsikini, Polysois Makras, Dimitrios Papadogias, Alexandra Stathopoulou, Kostas Tziveriotis, Konstantina Dimitriou
Publikováno v:
Clinical Endocrinology. 67:917-922
Summary Background Previous retrospective studies have suggested that women with acromegaly may present with menstrual irregularity and symptoms/signs of hyperandogenism, a phenotype similar to that of the polycystic ovary syndrome (PCOS). Objective
Autor:
George Piaditis, Dimitrios Papadogias, George Kontogeorgos, Polyzois Makras, Gregory Kaltsas, Kostantinos Kossivakis
Publikováno v:
European Journal of Gastroenterology & Hepatology. 19:1154-1159
We describe a 53-year-old male patient, with a known history of metastatic carcinoid tumour of the lung, who developed a variety of symptoms of the carcinoid syndrome and subsequently a carcinoid crisis. Although bronchial carcinoid tumours are very
Publikováno v:
HORMONES. 5:231-250
Cushing's syndrome (CS) is a physically and psychologically disabling disease associated with high morbidity resulting from inappropriate elevation of circulating free cortisol levels. The main features of CS are disturbance of the normal circadian r
Autor:
Ashley B. Grossman, Dimitrios Papadogias, Ioannis Griniatsos, Gregory Kaltsas, Polyzois Makras
Publikováno v:
Current Opinion in Endocrinology and Diabetes. 13:356-361
Autor:
Dimitrios Papadogias, Theodora Kounadi, George Piaditis, Kostas Kossyvakis, Kaity Tsigou, Kyriakos Vamvakidis, Athina Markou
Publikováno v:
HORMONES. 4:226-230
We present a 39-year old female with a benign adrenal tumor characterized by autonomous secretion of cortisol, androgens, and aldosterone. The patient presented with a 4-year history of hypertension and severe hirsutism. Baseline investigations revea
Publikováno v:
Pituitary. 8:169-174
Langerhans cell histocytosis (LCH) is a rare disease which exhibits a particular predilection for pituitary involvement leading to diabetes insipidus (DI) and other anterior pituitary hormonal deficiencies that are usually permanent and unresponsive
Publikováno v:
HORMONES. 2:217-228
Until the last decade, the diagnosis of GH deficiency (GHD) in adults was only considered as a marker of hypothalamo-pituitary disease. GHD in adults is now recognized as a specific clinical syndrome associated with a cluster of cardiovascular risk f
Autor:
Aggeliki Gouli, Polyzois Makras, Dimitrios Papadogias, Despina Ragkou, Georgios Zografos, Gregory Kaltsas, Georgios Chrousos, Ioannis I. Androulakis, G. Piaditis, Athina Markou, Kyriakos Vamvakidis, Konstantina Dimitriou
Publikováno v:
Clinical endocrinology. 71(6)
Summary Objectives Previous studies based on standard endocrine testing have shown a variable incidence of autonomous cortisol secretion (ACS) or autonomous aldosterone secretion (AAS) in patients with single adrenal adenomas (SAA). We tested whether
Publikováno v:
European journal of endocrinology / European Federation of Endocrine Societies. 151(1)
Neuroendocrine tumours (NETs) constitute a heterogeneous group of tumours that are able to express cell membrane neuroamine uptake mechanisms and/or specific receptors, such as somatostatin receptors, which can be of great value in the localization a
Autor:
Dimitrios Papadogias
Publikováno v:
Current Opinion in Endocrinology & Diabetes; Aug2006, Vol. 13 Issue 4, p356-361, 6p