Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Iraklis, Vainas"'
Autor:
Kalliopi Pazaitou-Panayiotou, Gregory Kaltsas, Iraklis Vainas, Alexandra Chrisoulidou, Konstantinos Lytras, Ioannis Iakovou, Eleni Georgiou, Maria Boudina
Publikováno v:
Endocrine Research. 35:137-143
Introduction. We studied the function of hypothalamic–pituitary–adrenal (HPA) axis in females with differentiated thyroid cancer (DTC) and its sequelae on metabolism and cardiovascular risk. Methods and Results. Sixteen women were investigated wi
Autor:
Iosif Kelesidis, Kalliopi Pazaitou-Panayiotou, Aris Mpousoulegas, Iraklis Vainas, Catherine J. Williams, Theodore Kelesidis, Athina Kaprara, Jennifer Blakeman, Christos S. Mantzoros
Publikováno v:
European Journal of Endocrinology. 156:187-194
Objective: Several components of the GH and IGF systems have been implicated in the development of malignancies. All components of these hormonal systems have never been jointly evaluated in female breast cancer, and previous studies have not examine
Autor:
Charicleia Destouni, Despoina Malle, Kalliopi Pazaitou-Panajiotou, Rosalia-Maria Valeri, Iraklis Vainas, Anastasia Kiziridou
Publikováno v:
Acta Cytologica. 50:23-27
Objective To investigate the efficacy of the ThinPrep Processor (Cytyc Corporation, Boxborough, Massachusetts, U.S.A) in fine needle aspiration (FNA) of thyroid gland lesions. Study design This study included 459 thyroid FNA specimens obtained from p
Autor:
Eleni Georgiou, Grammati Galaktidou, Maria Boudina, Ekaterini Raptou, Apostolos Drimonitis, Athina Kaprara, Iraklis Vainas, Kalliopi Pazaitou-Panayiotou
Publikováno v:
HORMONES. 4:213-220
OBJECTIVE: To define clinical presentation, surgical complications, follow-up characteristics, and survival of 23 children and adolescents with thyroid carcinoma. DESIGN: Retrospective analysis of data of 23 children and adolescents with thyroid carc
Autor:
Kalliopi Pazaitou-Panayiotou, Frideriki Patakiouta, Athina Kaprara, Maria Boudina, Eleni Georgiou, Alexandra Chrisoulidou, Iraklis Vainas, Apostolos Drimonitis
Publikováno v:
Endocrine Journal. 52:653-657
Brain metastasis is an uncommon complication of differentiated thyroid carcinoma. Even more, cerebellar metastases from papillary thyroid carcinoma (PTC) are exceptional. We report a 69-year-old male patient with infiltrative PTC who developed high l
Autor:
Eudoxia Ginikopoulou, Alexandra Chrisoulidou, Jakob Angel, Chariclia Destouni, Kalliopi Pazaitou, Iraklis Vainas
Publikováno v:
Thyroid. 12:1137-1140
We report on three cases with rapidly increasing thyroid masses who were referred with the provisional diagnosis of thyroid carcinoma. In the two cases, the diagnosis of tuberculosis was established after thyroidectomy, but in the third case diagnosi
Autor:
Petros Perros, George Siardos, Frideriki Patakiouta, Iraklis Vainas, Apostolos Drimonitis, Kalliopi Pazaitou-Panayiotou, Maria Boudina
Publikováno v:
European journal of endocrinology. 159(6)
BackgroundThyroid carcinoma has been reported in patients operated for different types of hyperthyroidism and the probability of a hot nodule being malignant seems to be low. The aim of the present study was to explore the relationship between thyroi
Autor:
Kalliopi Pazaitou-Panayiotou, Frideriki Patakiouta, Eleni Georgiou, Ioannis Efstratiou, Maria Boudina, Alexandra Chrisoulidou, Iraklis Vainas, Ioannis Iakovou, George Kontogeorgos
Publikováno v:
Hormones (Athens, Greece). 7(3)
Ectopic production of CRH by a medullary thyroid carcinoma or its metastases is a rare cause of ectopic Cushing’s syndrome (ECS). We report a 45-year old male with medullary thyroid carcinoma (MTC), who, 24 years following the initial diagnosis, pr
Autor:
Kalliopi, Pazaitou-Panayiotou, Athina, Kaprara, Leda, Sarika, Thanasis, Zovoilis, Ioulia, Belogianni, Iraklis, Vainas, Georgios, Nasioulas
Publikováno v:
Anticancer research. 25(3B)
Multiple Endocrine Neoplasia type 2 (MEN 2) is an autosomal dominant inherited syndrome characterized by a strong predisposition for developing endocrine tumors. MEN 2 is caused by germline mutations in the ret proto-oncogene. We investigated the fea