المؤلفون: Özboyacı, Evren

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Kardiyolojisi Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Pediatrik Endokrinoloji Anabilim Dalı., orcid:0000-0002-6598-8262, Uysal, Fahrettin, Bostan, Özlem Mehtap, Saǧlam, Halil, Semizel, Evren, Çil, Ergün, AAH-4421-2021, GLN-8241-2022, AAH-3865-2021, AAG-8558-2021, 24469008200, 8676936500, 35612700100, 12646191300, 35587943300

مصطلحات موضوعية: Children, Type 1 diabetes mellitus, Electrocardiography, Qtc dispersion, P dispersion, Qt dispersion, P-wave, Mortality, Failure, Risk, Insulin, Pediatrics, Adolescent, Autonomic nervous system diseases, Case-control studies, Child, Diabetes mellitus, type 1, Early diagnosis, Female, Humans, Male, Sensitivity and specificity, Peripheral Nervous System Diseases, Heart Rate Variability, Autonomic Neuropathy, Adult, Age distribution, Article, Autonomic dysfunction

العلاقة: Makale - Uluslararası Hakemli Dergi; Pediatrics International; Sanayi; Uysal, F. vd. (2014). "Evaluation of electrocardiographic parameters for early diagnosis of autonomic dysfunction in children and adolescents with type-1 diabetes mellitus". Pediatrics International, 56(5), 675-680.; https://doi.org/10.1111/ped.12329Test; https://hdl.handle.net/11452/39792Test; 000344243200011; 2-s2.0-84908244682; 675; 680; 56

الإتاحة: https://doi.org/10.1111/ped.12329Test
https://hdl.handle.net/11452/39792Test

المؤلفون: Sarı, Esin Söğütlü, Yazıcı, Alper, Eser, Betül, Erol, Muhammet Kazım, Kılıç, Adil, Ermiş, Sıtkı Samet, Koytak, Arif, Akşıt, Hasan

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Yakut, Tahsin, 6602802424

مصطلحات موضوعية: 4G/5G polymorphism of PAI-1 gene, Central serous chorioretinopathy, Serum PAI-1 level, Promoter, Abnormalities, Risk, Ophthalmology, Toxicology, Adult, Female, Gene frequency, Genotype, Humans, Male, Middle aged, Plasminogen activator inhibitor 1, Polymorphism, genetic, Prevalence, Risk factors, Turkey, Central Serous Retinopathy, Fluorescence Angiography, Verteporfin, Genomic DNA, SERPINE1 protein, human, Article, Body mass, Clinical article

العلاقة: Makale - Uluslararası Hakemli Dergi; Cutaneous and Ocular Toxicology; Yurt içi; Sanayi; Sarı, E. S. vd. (2014). "The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels". Cutaneous and Ocular Toxicology, 33(4), 270-274.; 556-9535; https://doi.org/10.3109/15569527.2013.854372Test; http://hdl.handle.net/11452/27175Test; 000345498400002; 2-s2.0-84912100853; 270; 274; 33

الإتاحة: https://doi.org/10.3109/15569527.2013.854372Test
http://hdl.handle.net/11452/27175Test

المؤلفون: Sarı, Esin Söğütlü, Yazıcı, Alper, Eser, Betül, Erol, Muhammet Kazım, Kılıç, Adil, Ermiş, Sıtkı Samet, Koytak, Arif, Akşıt, Hasan

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Yakut, Tahsin, 6602802424

مصطلحات موضوعية: 4G/5G polymorphism of PAI-1 gene, Central serous chorioretinopathy, Serum PAI-1 level, Promoter, Abnormalities, Risk, Ophthalmology, Toxicology, Adult, Female, Gene frequency, Genotype, Humans, Male, Middle aged, Plasminogen activator inhibitor 1, Polymorphism, genetic, Prevalence, Risk factors, Turkey, Central Serous Retinopathy, Fluorescence Angiography, Verteporfin, Genomic DNA, SERPINE1 protein, human, Article, Body mass, Clinical article

العلاقة: Makale - Uluslararası Hakemli Dergi; Cutaneous and Ocular Toxicology; Yurt içi; Sanayi; Sarı, E. S. vd. (2014). "The prevalence of 4G/5G polymorphism of plasminogen activator inhibitor-1 (PAI-1) gene in central serous chorioretinopathy and its association with plasma PAI-1 levels". Cutaneous and Ocular Toxicology, 33(4), 270-274.; 556-9535; https://doi.org/10.3109/15569527.2013.854372Test; http://hdl.handle.net/11452/27175Test; 000345498400002; 2-s2.0-84912100853; 270; 274; 33

الإتاحة: https://doi.org/10.3109/15569527.2013.854372Test
http://hdl.handle.net/11452/27175Test

المؤلفون: Özçimen, Ahmet Ata

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji ve Romatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Fiziksel Tıp ve Rehabilitasyon Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Psikiyatri Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nöroloji Anabilim Dalı., orcid:0000-0003-0463-6818, orcid:0000-0003-4436-3797, Dilek, Kamil, Bingöl, Ümit, Sarıcaoğlu, Hayriye, Sarandöl, Aslı, Taşkapılıoğlu, Özlem, Yurtkuran, Merih M., Yurtkuran, Mustafa Abbas, Oral, Haluk Barbaros, AAK-6623-2020, K-7285-2012, X-4479-2018, 56005080200, 6507727900, 6603722836, 14020405100, 23037226400, 55408539300, 7003389525, 7004498001

مصطلحات موضوعية: Genetics & heredity, Immunology, Interleukin-1 receptor antagonist, Inflammatory-bowel-disease, Ifn-gamma gene, In-vitro, Nucleotide-sequence, Cytokine production, Online databases, Long arm, Association, Risk, Adult, Behcet syndrome, Female, Gene frequency, Genetic predisposition to disease, Genotype, Humans, Interleukin-1, Male, Middle aged, Multigene Family, Polymorphism, genetic, single nucleotide, Turkey, Uveitis, Infliximab, Interleukin 1 receptor

العلاقة: Makale - Uluslararası Hakemli Dergi; T-2004/59; International Journal of Immunogenetics; Yurt içi; Özçimen, A. A. vd. (2011). "IL-1 cluster gene polymorphisms in Turkish patients with Behçet's disease". International Journal of Immunogenetics, 38(4), 295-301.; https://doi.org/10.1111/j.1744-313X.2011.01006.xTest; http://hdl.handle.net/11452/23505Test; 000292335800005; 2-s2.0-79959944004; 295; 301; 38

الإتاحة: https://doi.org/10.1111/j.1744-313X.2011.01006.xTest
http://hdl.handle.net/11452/23505Test

المؤلفون: Özçimen, Ahmet Ata

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Mikrobiyoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji ve Romatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Fiziksel Tıp ve Rehabilitasyon Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Dermatoloji Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Psikiyatri Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nöroloji Anabilim Dalı., orcid:0000-0003-0463-6818, orcid:0000-0003-4436-3797, Dilek, Kamil, Bingöl, Ümit, Sarıcaoğlu, Hayriye, Sarandöl, Aslı, Taşkapılıoğlu, Özlem, Yurtkuran, Merih M., Yurtkuran, Mustafa Abbas, Oral, Haluk Barbaros, AAK-6623-2020, K-7285-2012, X-4479-2018, 56005080200, 6507727900, 6603722836, 14020405100, 23037226400, 55408539300, 7003389525, 7004498001

مصطلحات موضوعية: Genetics & heredity, Immunology, Interleukin-1 receptor antagonist, Inflammatory-bowel-disease, Ifn-gamma gene, In-vitro, Nucleotide-sequence, Cytokine production, Online databases, Long arm, Association, Risk, Adult, Behcet syndrome, Female, Gene frequency, Genetic predisposition to disease, Genotype, Humans, Interleukin-1, Male, Middle aged, Multigene Family, Polymorphism, genetic, single nucleotide, Turkey, Uveitis, Infliximab, Interleukin 1 receptor

العلاقة: Makale - Uluslararası Hakemli Dergi; T-2004/59; International Journal of Immunogenetics; Yurt içi; Özçimen, A. A. vd. (2011). "IL-1 cluster gene polymorphisms in Turkish patients with Behçet's disease". International Journal of Immunogenetics, 38(4), 295-301.; https://doi.org/10.1111/j.1744-313X.2011.01006.xTest; http://hdl.handle.net/11452/23505Test; 000292335800005; 2-s2.0-79959944004; 295; 301; 38

الإتاحة: https://doi.org/10.1111/j.1744-313X.2011.01006.xTest
http://hdl.handle.net/11452/23505Test