Zobrazeno 1 - 10
of 209
pro vyhledávání: '"Doudounakis, S"'
Autor:
GIANNAKOPOULOS, A., VALIAKOS, G., PAPASPYROPOULOS, K., DOUGAS, G., KOROU, L. M., TASIOUDI, K. E., FTHENAKIS, G. C., HUTCHINGS, M. R., KAIMARAS, D., TSOKANA, C. N., ILIADOU, P., SPYROU, V., TZANI, M., BIRTSAS, P., KOSTOGLOU, P., SOKOS, C., DOUDOUNAKIS, S., YON, L., HANNANT, D., ARTOIS, M., TSIODRAS, S., HADJICHRISTODOULOU, C., BILLINIS, C.
Publikováno v:
Epidemiology and Infection, 2016 Oct 01. 144(14), 3068-3079.
Externí odkaz:
https://www.jstor.org/stable/26515834
Autor:
Giannakopoulos, A. Katelaris, A. Noni, M. Karakonstantakis, T. Kanaka-Gantenbein, C. Doudounakis, S.
Patients with cystic fibrosis (CF) commonly present with an elevated TSH concentration, suggesting subclinical hypothyroidism. Its relation to concomitant pancreatic insufficiency and its natural course upon initiation of enzyme replacement have not
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::a480ecac6e64c90db9f29408ff8d7431
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3123447
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3123447
Species of the Scedosporium apiospermum complex are the second most frequent filamentous fungi after Aspergillus fumigatus that can be found in cystic fibrosis (CF). Mixed colonisation by S. apiospermum complex and A. fumigatus is also quite common.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::14576138580565be451efe9c13efb7b4
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3125879
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3125879
Aim: Data about immunisation rates in cystic fibrosis (CF) patients are scarce. We estimated the rates and timeliness of immunisations in CF patients aged 0.55–22 years. Methods: We studied 122 subjects at a hospital in Greece in 2014. A standard q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c8846ac889906509b724e1acce15c1ee
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3126393
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3126393
Autor:
Petrocheilou, A. Papagrigoriou-Theodoridou, M. Michos, A. Doudounakis, S.-E. Loukou, I. Kaditis, A.
Lung disease in cystic fibrosis (CF) starts early, with studies identifying abnormalities on chest computed tomography (CT) scan even in infancy. In this retrospective study, abnormal chest CT was the main outcome; body mass index (BMI) z score and f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c0e64a7ab4196cf60afb67714002b1ee
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2988058
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2988058
Autor:
Doulgeraki, A. Petrocheilou, A. Petrocheilou, G. Chrousos, G. Doudounakis, S.-E. Kaditis, A.G.
The aim of this study was to explore whether history of meconium ileus (MI) at birth in children and adolescents with cystic fibrosis (CF) adversely affects body composition and lung function in later life. Data of children and adolescents with CF wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::24e0337f501f12d626f6645cb3d342e9
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3126107
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3126107
Background Allergic bronchopulmonary aspergillosis (ABPA) and Aspergillus fumigatus sensitization (AFS) are quite often observed in cystic fibrosis (CF) patients. The aim of this study was to evaluate the use of basophil activation test (BAT) in thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d05806b40b9341d7d178ceda2da65f23
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3100908
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3100908
The objectives of this work were (i) geographical analysis of the 2012-2014 outbreak of rabies in Greece using GIS and (ii) comparative analysis of animal cases with data of potential human exposure to rabies together with environmental data, in orde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::e9e6835f877d05d070e7966941b326f5
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3171391
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3171391
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Candida albicans is increasingly recognised as a coloniser of the respiratory tract in cystic fibrosis (CF) patients. Yet, the potential role, if any, of the micro-organism in the progress of the disease remains unclear. In this study, we investigate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::8e19674c0d14fccce8d3562336887621
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3125090
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3125090