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: Topaloğlu, Rezan, Baskın, Esra, Bahat, Elif, Kavukçu, Salih, Çakar, Nilgün, Güven, Ayfer Gür, Çalışkan, Salim, Erdoğan, Özlem, Yalçınkaya, Fatoş

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Pediatrik Nefroloji Anabilim Dalı., Dönmez, Osman, AAA-8778-2021, 19033971800

مصطلحات موضوعية: Urology & nephrology, Bartter's syndrome, Cystinosis, Demography, Failure to thrive, Features, Gitelman's syndrome, Hereditary renal tubular disorders, Prevalence, PRTA, Acidosis, Mutations, Deafness, Child, preschool, Consanguinity, Female, Humans, Infant, Kidney diseases, Kidney tubules, Male, Questionnaires, Turkey, Erythrocyte Anion Exchange Protein 1, Renal Tubular Acidosis, Kidney Calcification, Adolescent, Adult, Age distribution

العلاقة: Makale - Uluslararası Hakemli Dergi; Clinical and Experimental Nephrology; Yurt içi; Sanayi; Topaloğlu, R. vd. (2011). "Hereditary renal tubular disorders in Turkey: Demographic, clinical, and laboratory features". Clinical and Experimental Nephrology, 15(1), 108-113.; https://doi.org/10.1007/s10157-010-0367-zTest; https://link.springer.com/article/10.1007/s10157-010-0367-zTest; http://hdl.handle.net/11452/24513Test; 000287452800016; 2-s2.0-79952196349; 108; 113; 15

الإتاحة: https://doi.org/10.1007/s10157-010-0367-zTest
http://hdl.handle.net/11452/24513Test

المساهمون: Bursa Uludağ Üniversitesi/Tıp Fakültesi/ Tıbbi biyoloji Anabilim Dalı, Bursa Uludağ Üniversitesi/Tıp Fakültesi/ Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı ve Onkoloji Bilim Dalı, orcid:0000-0002-0910-4258, Erdem, Ecem Efendi, Çeçener, Gülşah, Ünlü, Havva Tezcan, Evim, Melike Sezgin, GYU-0252-2022, ESY-2704-2022, AAP-9988-2020, AAH-1452-2021, 57223043925, 6508156530, 57223050102, 36337796600

مصطلحات موضوعية: Philadelphia-like, Acute lymphoblastic leukemia, Pediatric, Progress, Chıldren, Pediatrics, Philadelphia 1 Chromosome, BCR ABL protein, Olanzapine, Thymic stromal lymphopoietin, Adult, Burkitt lymphoma, Cancer prognosis, Case report, Chemiluminescence, Immunoassay, Child, Clinical article, Clinical evaluation, Controlled study, Flow cytometry, Fluorescence in situ, Hybridization, Gene expression profiling, Gene mutation, Health care personnel, Heart ejection fraction, Hematopoietic cell, Human, Human cell

العلاقة: Makale - Uluslararası Hakemli Dergi; Guncel Pediatri; Yurt içi; Erdem, E. E. vd. (2021) "Philadelphia-like acute lymphoblastic leukemia in pediatric cases". Güncel Pediatri, 19(1), 141-150.; https://doi.org/10.4274/jcp.2020.0020Test; https://cms.galenos.com.tr/Uploads/Article_48534/G%C3%BCncel%20Pediatri-18-220-En.pdfTest; https://hdl.handle.net/11452/39052Test; 000735332200020; 2-s2.0-85104633068; 141; 150; 19

الإتاحة: https://doi.org/10.4274/jcp.2020.0020Test
https://hdl.handle.net/11452/39052Test
https://cms.galenos.com.tr/Uploads/Article_48534/G%C3%BCncel%20Pediatri-18-220-En.pdfTest

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı., Karkucak, Mutlu, Sağ, Şebnem Özemri, Yakut, Tahsin, Kimya, Yalçın, AAH-8355-2021, 35388323500, 36638231300, 6602802424, 6603919968

مصطلحات موضوعية: Prenatal diagnosis, Translocation, Aneuploidy, Sperm FISH, Genetic counseling, In-sıtu hybridization, Constitutional, Rearrangements, Chromosomal-aberrations, Fragile sites, Carriers, Breakpoints, Amniocentesis, Genetics & heredity, Wolf-Hirschhorn Syndrome, Phenotype, EF Hand Motif, Adult, Article, Case report, Chromosome 11p, Chromosome 13, Chromosome 18, Chromosome 21, Chromosome 21q, Chromosome G band, Chromosome polymorphism, Chromosome translocation 1, Chromosome translocation 12, Female

العلاقة: Makale - Uluslararası Hakemli Dergi; International Journal of Human Genetics; Karkucak, M. vd. (2010). "Prenatal diagnosis of de novo reciprocal translocation t(1;12)(q21.3;p11.2) with trisomy 21 and sperm FISH analysis for increased aneuploidy risk". International Journal of Human Genetics, 10(4), 231-234.; https://doi.org/10.1080/09723757.2010.11886110Test; http://hdl.handle.net/11452/24978Test; 000287340400004; 2-s2.0-79953273937; 231; 234; 10

الإتاحة: https://doi.org/10.1080/09723757.2010.11886110Test
http://hdl.handle.net/11452/24978Test

المؤلفون: Yılmaz, Yusuf

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı., Ölmez, Ömer Fatih, Gürel, Selim, 26435400000, 7003706434

مصطلحات موضوعية: Chronic hepatitis B, Chronic hepatitis C, Histopathology, Iron, Prohepcidin, Iron stores, Expression, Infection, Gastroenterology & hepatology, Adult, Aged, Antimicrobial cationic peptides, Case-control studies, Female, Hepatitis B, chronic, Hepatitis C, Humans, Liver cirrhosis, Male, Middle aged, Protein precursors, Young adult, Hepcidins, Metal Transporting Protein 1, Iron-Refractory Iron Deficiency Anemia, Hepcidin, Article, Controlled study, Disease association

العلاقة: Makale - Uluslararası Hakemli Dergi; European Journal of Gastroenterology and Hepatology; Ölmez, Ö. F. vd. (2010). "Plasma prohepcidin levels in patients with chronic viral hepatitis: Relationship with liver fibrosis". European Journal of Gastroenterology and Hepatology, 22(4), 461-465.; https://doi.org/10.1097/MEG.0b013e3283344708Test; https://pubmed.ncbi.nlm.nih.gov/19940783Test/; http://hdl.handle.net/11452/25370Test; 000276566100012; 2-s2.0-77949439229; 461; 465; 22

الإتاحة: https://doi.org/10.1097/MEG.0b013e3283344708Test
http://hdl.handle.net/11452/25370Test
https://pubmed.ncbi.nlm.nih.gov/19940783Test/

المؤلفون: Kline-Fath, Beth M., Laor, Tal, Tinkle, Brad T.

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Radyoloji Anabilim Dalı., Yazıcı, Zeynep, AAI-2303-2021, 6701668723

مصطلحات موضوعية: Prenatal imaging, Skeletal dysplasia, Musculoskeletal, Fetal MRI, Pediatrics, Radiology, nuclear medicine & medical imaging, Cartilage diseases, Female, Humans, Magnetic resonance imaging, Osteochondrodysplasias, Prenatal Diagnosis, Type 1 Stickler Syndrome, Congenita Spondyloepiphyseal Dysplasia, Metatropic Dwarfism, Collagen type 2, Collagen type 2a1, Unclassified drug, Adult, Amniocentesis, Article, Case report, Chondrodysplasia, Clubfoot, Epiphysis disease, Fetus, Fetus echography, Fetus karyotyping, Genetic screening

العلاقة: Makale - Uluslararası Hakemli Dergi; Pediatric Radiology; Yurt dışı; Sanayi; Yazıcı, Z. vd. (2010). "Fetal MR imaging of Kniest dysplasia". Pediatric Radiology, 40(3), 348-352.; https://doi.org/10.1007/s00247-009-1444-xTest; https://link.springer.com/article/10.1007/s00247-009-1444-xTest; http://hdl.handle.net/11452/25417Test; 000274386700010; 2-s2.0-77951022914; 348; 352; 40

الإتاحة: https://doi.org/10.1007/s00247-009-1444-xTest
http://hdl.handle.net/11452/25417Test

المؤلفون: Yılmaz, Yusuf

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı., Ölmez, Ömer Fatih, Gürel, Selim, 26435400000, 7003706434

مصطلحات موضوعية: Chronic hepatitis B, Chronic hepatitis C, Histopathology, Iron, Prohepcidin, Iron stores, Expression, Infection, Gastroenterology & hepatology, Adult, Aged, Antimicrobial cationic peptides, Case-control studies, Female, Hepatitis B, chronic, Hepatitis C, Humans, Liver cirrhosis, Male, Middle aged, Protein precursors, Young adult, Hepcidins, Metal Transporting Protein 1, Iron-Refractory Iron Deficiency Anemia, Hepcidin, Article, Controlled study, Disease association

العلاقة: Makale - Uluslararası Hakemli Dergi; European Journal of Gastroenterology and Hepatology; Ölmez, Ö. F. vd. (2010). "Plasma prohepcidin levels in patients with chronic viral hepatitis: Relationship with liver fibrosis". European Journal of Gastroenterology and Hepatology, 22(4), 461-465.; https://doi.org/10.1097/MEG.0b013e3283344708Test; https://pubmed.ncbi.nlm.nih.gov/19940783Test/; http://hdl.handle.net/11452/25370Test; 000276566100012; 2-s2.0-77949439229; 461; 465; 22

الإتاحة: https://doi.org/10.1097/MEG.0b013e3283344708Test
http://hdl.handle.net/11452/25370Test
https://pubmed.ncbi.nlm.nih.gov/19940783Test/

المؤلفون: Kline-Fath, Beth M., Laor, Tal, Tinkle, Brad T.

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Radyoloji Anabilim Dalı., Yazıcı, Zeynep, AAI-2303-2021, 6701668723

مصطلحات موضوعية: Prenatal imaging, Skeletal dysplasia, Musculoskeletal, Fetal MRI, Pediatrics, Radiology, nuclear medicine & medical imaging, Cartilage diseases, Female, Humans, Magnetic resonance imaging, Osteochondrodysplasias, Prenatal Diagnosis, Type 1 Stickler Syndrome, Congenita Spondyloepiphyseal Dysplasia, Metatropic Dwarfism, Collagen type 2, Collagen type 2a1, Unclassified drug, Adult, Amniocentesis, Article, Case report, Chondrodysplasia, Clubfoot, Epiphysis disease, Fetus, Fetus echography, Fetus karyotyping, Genetic screening

العلاقة: Makale - Uluslararası Hakemli Dergi; Pediatric Radiology; Yurt dışı; Sanayi; Yazıcı, Z. vd. (2010). "Fetal MR imaging of Kniest dysplasia". Pediatric Radiology, 40(3), 348-352.; https://doi.org/10.1007/s00247-009-1444-xTest; https://link.springer.com/article/10.1007/s00247-009-1444-xTest; http://hdl.handle.net/11452/25417Test; 000274386700010; 2-s2.0-77951022914; 348; 352; 40

الإتاحة: https://doi.org/10.1007/s00247-009-1444-xTest
http://hdl.handle.net/11452/25417Test

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı., Karkucak, Mutlu, Sağ, Şebnem Özemri, Yakut, Tahsin, Kimya, Yalçın, AAH-8355-2021, 35388323500, 36638231300, 6602802424, 6603919968

مصطلحات موضوعية: Prenatal diagnosis, Translocation, Aneuploidy, Sperm FISH, Genetic counseling, In-sıtu hybridization, Constitutional, Rearrangements, Chromosomal-aberrations, Fragile sites, Carriers, Breakpoints, Amniocentesis, Genetics & heredity, Wolf-Hirschhorn Syndrome, Phenotype, EF Hand Motif, Adult, Article, Case report, Chromosome 11p, Chromosome 13, Chromosome 18, Chromosome 21, Chromosome 21q, Chromosome G band, Chromosome polymorphism, Chromosome translocation 1, Chromosome translocation 12, Female

العلاقة: Makale - Uluslararası Hakemli Dergi; International Journal of Human Genetics; Karkucak, M. vd. (2010). "Prenatal diagnosis of de novo reciprocal translocation t(1;12)(q21.3;p11.2) with trisomy 21 and sperm FISH analysis for increased aneuploidy risk". International Journal of Human Genetics, 10(4), 231-234.; https://doi.org/10.1080/09723757.2010.11886110Test; http://hdl.handle.net/11452/24978Test; 000287340400004; 2-s2.0-79953273937; 231; 234; 10

الإتاحة: https://doi.org/10.1080/09723757.2010.11886110Test
http://hdl.handle.net/11452/24978Test

المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Nefroloji ve Romatoloji Anabilim Dalı., orcid:0000-0003-4518-5283, Arabul, Mahmut, Güllülü, Mustafa, Yılmaz, Yusuf, Akdağ, İbrahim, Kahvecioğlu, Serdar, Eren, Mehmet Ali, Dilek, Kamil, ABH-7279-2020, 15925230900, 6602684544, 22936014300, 8342488100, 55956719500, 7006788432, 56005080200

مصطلحات موضوعية: Medical laboratory technology, Anemia, End-stage renal disease, Inflammation, Prohepcidin, Statins, Chronic kidney-disease, Iron-metabolism, Hepcidin, Adult, Antimicrobial cationic peptides, C-reactive protein, Dyslipidemias, Fatty acids, monounsaturated, Female, Humans, Indoles, Kidney failure, chronic, Lipids, Male, Middle aged, Protein precursors, Renal dialysis, Hepcidins, Metal Transporting Protein 1, Iron-Refractory Iron Deficiency Anemia, Fluindostatin, Low density lipoprotein cholesterol

العلاقة: Makale - Uluslararası Hakemli Dergi; Clinical Biochemistry; Arabul, M. vd. (2008). ''Effect of fluvastatin on serum prohepcidin levels in patients with end-stage renal disease''. Clinical Biochemistry, 41(13), 1055-1058.; https://doi.org/10.1016/j.clinbiochem.2008.05.010Test; https://www.sciencedirect.com/science/article/pii/S0009912008002191Test; http://hdl.handle.net/11452/24987Test; 000258814500006; 2-s2.0-49349094167; 1055; 1058; 41; 13

الإتاحة: https://doi.org/10.1016/j.clinbiochem.2008.05.010Test
http://hdl.handle.net/11452/24987Test
https://www.sciencedirect.com/science/article/pii/S0009912008002191Test