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anna galili
(1 results)?
Endothelial nitric oxide synthase polymorphism (G894T) and nonarteritic anterior ischemic optic neuropathy.
Vis Neurosci. 2010 Nov;27(5-6):183-5. doi: 10.1017/S0952523810000350. Epub 2010 Nov 15.
Vis Neurosci. 2010.
PMID: 21073768
Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations.
Bouba I, Siomou E, Stefanidis CJ, Emmanouilidou A, Galidi A, Hatzi E, Markoula S, Mitsioni A, Siamopoulou A, Georgiou I.
Bouba I, et al. Among authors: galidi a.
Pediatr Nephrol. 2009 Aug;24(8):1569-72. doi: 10.1007/s00467-009-1140-y. Epub 2009 Mar 3.
Pediatr Nephrol. 2009.
PMID: 19255789
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Association of serum and follicular fluid SHBG levels and SHBG (TAAAA)n polymorphism with follicle size in women undergoing ovarian stimulation.
Hatzi E, Bouba I, Galidi A, Lazaros L, Xita N, Sakaloglou P, Kolios G, Bairaktari E, Kaponis A, Zikopoulos K, Tsatsoulis A, Georgiou I.
Hatzi E, et al. Among authors: galidi a.
Gynecol Endocrinol. 2011 Jan;27(1):27-32. doi: 10.3109/09513590.2010.493961. Epub 2010 Jun 14.
Gynecol Endocrinol. 2011.
PMID: 20540673
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Association of endothelial nitric oxide synthase polymorphism G894T with functional outcome in acute stroke patients.
Ellul J, Markoula S, Marousi S, Galidi A, Kyritsis AP, Papathanasopoulos P, Georgiou I.
Ellul J, et al. Among authors: galidi a.
Neurol Res. 2011 Oct;33(8):835-40. doi: 10.1179/1743132811Y.0000000011.
Neurol Res. 2011.
PMID: 22004707
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