Showing results 20 to 25 of 25
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Issue Date | Title | Author(s) |
2020 | Missense Genetic Polymorphisms of Microsomal (EPHX1) and Soluble Epoxide Hydrolase (EPHX2) and Their Relation to the Risk of Large Artery Atherosclerotic Ischemic Stroke in a Turkish Population | Can Demirdöğen, Birsen ; Miçooğulları, Yağmur; Özçelik, Aysun Türkanoğlu; Adalı, Orhan |
Oct-2019 | Paraoxonase 1 (PON1) promoter (-107T/C) and coding region (192Q/R and 55L/M) genetic variations in pseudoexfoliation syndrome and pseudoexfoliative glaucoma risk | Can, Demirdöğen Birsen ; Koçan Akçin, Canan; Göksoy, Ezgi; Yakar, Gizem; Öztepe, Tuğçe; Demirkaya-Budak, Sinem; Oflaz, Sinan |
Jul-2019 | Potential role of calcifying nanoparticles in the etiology of multiple sclerosis | Can, Demirdöğen Birsen |
2017 | Relationship between paraoxonase 1 (PON1) promoter (-107T/C) and coding region polymorphisms (192Q/R and 55L/M) and Pseudoexfoliation syndrome | Can Demirdöğen, Birsen ; Yakar, G.; Göksoy, E.; Demirkaya, S.; Koçan, Canan; Özge, G.; Mumcuoğlu, T. |
2022 | Single nucleotide variants around the connective tissue growth factor (CTGF/CCN2) gene and their association with multiple sclerosis risk, disability scores, and rate of disease progression | Can Demirdöğen, Birsen ; Kilic, Osman Oguzhan; Karagulle, Elif Naz; Kalmaz, Latife Mekselina; Mungan, Semra |
2016 | A study on the association between rs6918698 polymorphism in connective tissue growth factor gene and pseudoexfoliation syndrome | Koçan, Canan; Öztepe, T.; Özge, G.; Mumcuoğlu, T.; Can Demirdöğen, Birsen |