Browsing by Author Galidi, A.

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Showing results 1 to 5 of 5
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Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformationsBouba, I.; Siomou, E.; Stefanidis, C. J.; Emmanouilidou, A.; Galidi, A.; Hatzi, E.; Markoula, S.; Mitsioni, A.; Siamopoulou, A.; Georgiou, I.24-Nov-2015-
Association of endothelial nitric oxide synthase polymorphism G894T with functional outcome in acute stroke patientsEllul, J.; Markoula, S.; Marousi, S.; Galidi, A.; Kyritsis, A. P.; Papathanasopoulos, P.; Georgiou, I.24-Nov-2015-
Association of serum and follicular fluid SHBG levels and SHBG (TAAAA)n polymorphism with follicle size in women undergoing ovarian stimulationHatzi, E.; Bouba, I.; Galidi, A.; Lazaros, L.; Xita, N.; Sakaloglou, P.; Kolios, G.; Bairaktari, E.; Kaponis, A.; Zikopoulos, K.; Tsatsoulis, A.; Georgiou, I.24-Nov-2015-
Endothelial nitric oxide synthase polymorphism (G894T) and nonarteritic anterior ischemic optic neuropathyGiannopoulos, S.; Markoula, S.; Asproudis, I.; Galidi, A.; Nikas, A.; Kyritsis, A. P.; Georgiou, I.24-Nov-2015-
The (TAAAA)n polymorphism of the SHBG gene in men with the metabolic syndromeXita, N.; Milionis, H. J.; Galidi, A.; Lazaros, L.; Katsoulis, K.; Elisaf, M. S.; Georgiou, I.; Tsatsoulis, A.24-Nov-2015-