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Inherited and acquired thrombophilia in adults with retinal vascular occlusion: A systematic review and meta‐analysis
Romiti, Giulio Francesco, Corica, Bernadette, Borgi, Marco, Visioli, Giacomo, Pacella, Elena, Cangemi, Roberto, Proietti, Marco, Basili, Stefania, Raparelli, Valeria
Published in Journal of thrombosis and haemostasis (01.12.2020)
Published in Journal of thrombosis and haemostasis (01.12.2020)
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Role of the ABO Blood Groups as a Risk Factor for Retinal Vein Occlusion
Posch-Pertl, Laura, List, Wolfgang, Michelitsch, Monja, Pinter-Hausberger, Silke, Posch, Florian, Innauer, Felix, Renner, Wilfried, Weger, Martin
Published in Ophthalmic research (01.01.2023)
Published in Ophthalmic research (01.01.2023)
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Association of MMP2-1306C/T Polymorphism with Ischemic Retinal Vein Occlusion
Christodoulou, Aikaterini, Bagli, Eleni, Gazouli, Maria, Moschos, Marilita M., Kitsos, George
Published in Archives of medical research (01.10.2020)
Published in Archives of medical research (01.10.2020)
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Retinal vein occlusion: a form of venous thrombosis or a complication of atherosclerosis? A meta-analysis of thrombophilic factors
Janssen, Mirian C H, den Heijer, Martin, Cruysberg, Johannes R M, Wollersheim, Hub, Bredie, Sebastian J H
Published in Thrombosis and haemostasis (01.06.2005)
Published in Thrombosis and haemostasis (01.06.2005)
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Association study of high-frequency variants of MTHFR gene with retinal vein occlusion in a Spanish population
Fernández-Vega, Beatriz, Álvarez, Lydia, García, Montserrat, Artime, Enol, González Fernández, Adrián, Fernández-Vega, Carlos, Nicieza, Javier, Vega, José A., González-Iglesias, Héctor
Published in Ophthalmic genetics (04.07.2019)
Published in Ophthalmic genetics (04.07.2019)
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GENETIC ASSOCIATION BETWEEN ARTERIAL STIFFNESS-RELATED GENE POLYMORPHISMS IN BRVO AND CRVO PATIENTS IN A TURKISH POPULATION
Demir, Selim, Ortak, Hüseyin, Benli, İsmail, Alim, Sait, Bütün, İlknur, Güneş, Alper, Ateş, Ömer
Published in Retina (Philadelphia, Pa.) (01.10.2015)
Published in Retina (Philadelphia, Pa.) (01.10.2015)
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Plasma homocysteine levels, methylene tetrahydrofolate reductase A1298C gene polymorphism and risk of retinal vein thrombosis
Ghaznavi, Habib, Soheili, Zahra, Samiei, Shahram, Soltanpour, Mohammad Soleiman
Published in Blood coagulation & fibrinolysis (01.09.2016)
Published in Blood coagulation & fibrinolysis (01.09.2016)
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The prevalence of activated protein C (APC) resistance and factor V Leiden is significantly higher in patients with retinal vein occlusion without general risk factors. Case-control study and meta-analysis
Rehak, Matus, Rehak, Jiri, Müller, Marc, Faude, Susanne, Faude, Frank, Siegemund, Annelie, Krcova, Vera, Slavik, Ludek, Hasenclever, Dirk, Scholz, Markus, Wiedemann, Peter
Published in Thrombosis and haemostasis (01.05.2008)
Published in Thrombosis and haemostasis (01.05.2008)
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Lack of association of LOXL1 gene variants in Japanese patients with central retinal vein occlusion without clinically detectable pseudoexfoliation material deposits
Tanito, Masaki, Hara, Katsunori, Akahori, Masakazu, Harata, Ayano, Itabashi, Takeshi, Takai, Yasuyuki, Kaidzu, Sachiko, Ohira, Akihiro, Iwata, Takeshi
Published in Acta ophthalmologica (Oxford, England) (01.05.2015)
Published in Acta ophthalmologica (Oxford, England) (01.05.2015)
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Role of Inflammation-Related Gene Polymorphisms in Patients with Central Retinal Vein Occlusion
Maier, Richard, Steinbrugger, Iris, Haas, Anton, Selimovic, Maksida, Renner, Wilfried, El-Shabrawi, Yosuf, Werner, Christoph, Wedrich, Andreas, Schmut, Otto, Weger, Martin
Published in Ophthalmology (Rochester, Minn.) (01.06.2011)
Published in Ophthalmology (Rochester, Minn.) (01.06.2011)
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Role of the Vitamin K Epoxide Reductase Complex Subunit 1 (VKORC1) −1639G>A Gene Polymorphism in Patients with Retinal Vein Occlusion
Weger, Martin, Steinbrugger, Iris, Renner, Wilfried, Pöschl, Eva Maria, Brockmann, Tobias, Rabensteiner, Dieter Franz, El-Shabrawi, Yosuf, Haas, Anton
Published in Current eye research (01.12.2013)
Published in Current eye research (01.12.2013)
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Predictive value of the vitamin K epoxide reductase complex subunit 1 G-1639A and C1173T single nucleotide polymorphisms in retinal vein occlusion
Ortak, Huseyin, Söğüt, Erkan, Demir, Helin, Ardagil, Aylin, Benli, Ismail, Sahin, Semsettin
Published in Clinical & experimental ophthalmology (01.09.2012)
Published in Clinical & experimental ophthalmology (01.09.2012)
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Protective effect of paraoxonase 1 gene variant L55M in retinal vein occlusion
Ortak, Huseyin, Söğüt, Erkan, Ateş, Omer, Erkorkmaz, Unal, Benli, Ismail, Akbas, Ali, Demir, Selim, Ozyurt, Hüseyin
Published in Molecular vision (25.02.2013)
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Published in Molecular vision (25.02.2013)
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Genetic polymorphisms and retinal vein occlusion in an Italian population
De Polo, L., Maltese, P.E., Rigoni, E., Bertelli, M., Cecchin, S., Staurenghi, G., Stoppa, G.
Published in Genetics and molecular research (01.01.2015)
Published in Genetics and molecular research (01.01.2015)
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Increased prevalence of factor V Leiden in patients with retinal vein occlusion and under 60 years of age
Arsène, Sophie, Delahousse, Bénédicte, Regina, Sandra, Le Lez, Marie-Laure, Pisella, Pierre-Jean, Gruel, Yves
Published in Thrombosis and haemostasis (01.07.2005)
Published in Thrombosis and haemostasis (01.07.2005)
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