Zobrazeno 1 - 10
of 727
pro vyhledávání: '"Zintzaras E"'
Autor:
Aretha, D., Fligou, F., Kiekkas, P., Messini, C., Panteli, E., Zintzaras, E., Karanikolas, M.
Publikováno v:
In International Journal of Obstetric Anesthesia May 2017 30:30-38
Autor:
Stefanidis, I. *, Vainas, A., Giannaki, C.D., Dardiotis, E., Spanoulis, A., Sounidaki, M., Eleftheriadis, T., Liakopoulos, V., Karatzaferi, C., Sakkas, G.K., Zintzaras, E., Hadjigeorgiou, G.M.
Publikováno v:
In Sleep Medicine September 2015 16(9):1131-1138
Autor:
Stefanidis, I., Vainas, A., Dardiotis, E., Giannaki, C.D., Gourli, P., Papadopoulou, D., Vakianis, P., Patsidis, E., Eleftheriadis, T., Liakopoulos, V., Pournaras, S., Sakkas, G.K., Zintzaras, E., Hadjigeorgiou, G.M.
Publikováno v:
In Sleep Medicine December 2013 14(12):1381-1386
Although fresh frozen plasma (FFP) transfusions are common practice in neonatology, robust evidence on their use is lacking. The aim of this study was to systematically review the literature for data on the practice of FFP transfusions in neonates an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::8f1b620c934e9cd8805c0ff2e09ee79b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220902
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220902
Autor:
Halkiadakis, I. Tzimis, V. Gryparis, A. Markopoulos, I. Konstadinidou, V. Zintzaras, E. Tzakos, M.
• AIM: To evaluate the agreement of biomechanically corrected intraocular pressure (b-IOP) and central corneal thickness (CCT) measurements obtained with the updated Corvis ST tonometer versus Goldmann applanation tonometry (GAT) and optical-based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::9a49f9c1da3d041481379c4072d85b63
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220161
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3220161
Introduction: Parkinson's disease is a neurodegenerative disorder with a complex etiology coming from interactions between genetic and environmental factors. Research on Parkinson's disease genetics has been an effortful struggle, while new technolog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::97a964276f4c07f2d87243744c7af736
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3020431
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3020431
Autor:
Scalco, R. S., Lucia, A., Santalla, A., Martinuzzi, A., Vavla, M., Reni, G., Toscano, A., Musumeci, O., Voermans, N. C., Kouwenberg, C. V., Laforet, P., San-Millan, B., Vieitez, I., Siciliano, G., Kuhnle, E., Trost, R., Sacconi, S., Stemmerik, M. G., Durmus, H., Kierdaszuk, B., Wakelin, A., Andreu, A. L., Pinos, T., Marti, R., Quinlivan, R., Vissing, J., Baruch, N., Ortega, F. J., Martin, M. A., Navarro, C., Millan, B. S., Castelli, M., Zucchi, F., Bruno, C., Scalco, R., Hadjgeorgiou, G., Zintzaras, E., Vorgerd, M., Zulow, E., Haller, R., Oflazer, P., Pouget, J.
Publikováno v:
Orphanet Journal of Rare Diseases, 15
Orphanet Journal of Rare Diseases, 15, 1
Orphanet Journal of Rare Diseases
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
ABACUS. Repositorio de Producción Científica
Universidad Europea (UEM)
Scalco, R S, Lucia, A, Santalla, A, Martinuzzi, A, Vavla, M, Reni, G, Toscano, A, Musumeci, O, Voermans, N C, Kouwenberg, C V, Laforêt, P, San-Millán, B, Vieitez, I, Siciliano, G, Kühnle, E, Trost, R, Sacconi, S, Stemmerik, M G, Durmus, H, Kierdaszuk, B, Wakelin, A, Andreu, A L, Pinós, T, Marti, R, Quinlivan, R, Vissing, J & EUROMAC Consortium 2020, ' Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC) ', Orphanet Journal of Rare Diseases, vol. 15, no. 1, pp. 330 . https://doi.org/10.1186/s13023-020-01562-x
Orphanet Journal of Rare Diseases, 15, 1
Orphanet Journal of Rare Diseases
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
ABACUS. Repositorio de Producción Científica
Universidad Europea (UEM)
Scalco, R S, Lucia, A, Santalla, A, Martinuzzi, A, Vavla, M, Reni, G, Toscano, A, Musumeci, O, Voermans, N C, Kouwenberg, C V, Laforêt, P, San-Millán, B, Vieitez, I, Siciliano, G, Kühnle, E, Trost, R, Sacconi, S, Stemmerik, M G, Durmus, H, Kierdaszuk, B, Wakelin, A, Andreu, A L, Pinós, T, Marti, R, Quinlivan, R, Vissing, J & EUROMAC Consortium 2020, ' Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC) ', Orphanet Journal of Rare Diseases, vol. 15, no. 1, pp. 330 . https://doi.org/10.1186/s13023-020-01562-x
Background The European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC) was launched to register rare muscle glycogenoses in Europe, to facilitate recruitment for research trials and to learn about the phenotypes an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94adc6c623ddc8c601564aa98abbe03e
http://hdl.handle.net/11570/3184381
http://hdl.handle.net/11570/3184381
Autor:
Stefanidis, I., Tziastoudi, M., Tsironi, E. E., Dardiotis, E., Tachmitzi, S. V., Fotiadou, A., Pissas, G., Kytoudis, K., Sounidaki, M., Ampatzis, G., Mertens, P. R., Liakopoulos, V., Eleftheriadis, T., Hadjigeorgiou, Georgios M., Santos, M., Zintzaras, E.
Publikováno v:
Renal Failure, Vol 40, Iss 1, Pp 561-576 (2018)
Renal Failure
Ren Fail
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Renal Failure
Ren Fail
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
An association study was conducted to investigate the relation between 14 variants of glucose transporter 1 gene (SLC2A1) and the risk of type 2 diabetes (T2DM) leading to nephropathy. We also performed a meta-analysis of 11 studies investigating ass
Publikováno v:
In Computer Methods and Programs in Biomedicine 2007 85(3):267-272
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