Browsing by Author "Sezgin, Ilhan"
Now showing items 1-16 of 16
-
Adult height in Turkish patients with Turner syndrome without growth hormone treatment
Bereket, Abdullah; Turan, Serap; Elcioglu, Nursel; Hacihanefioglu, Seniha; Memioglu, Nihal; Bas, Firdevs; Bundak, Rueveyde; Darendeliler, Feyza; Guenoez, Huelya; Saka, Nurcin; Ercan, Oya; Arslanoglu, Ilknur; Isgueven, Pinar; Yildiz, Metin; Can, Sule; Oezerkan, Ebru; Coker, Mahmut; Darcan, Suekran; Oezkan, Behzat; Orbak, Zerrin; Oeztas, Sitki; Palanduez, Suekrue; Sezgin, Ilhan; Atabek, Emre; Erkul, Ibrahim; Erdogan, Guerbuez (TURKISH J PEDIATRICS, 2008)Spontaneous adult height (AH) in Turner syndrome (TS) varies among populations. Population-specific AH data is essential to assess the efficacy of growth-promoting therapies in TS. A multicenter study was performed to ... -
Analysis of HumFABP(2) as a polymorphic human genetic marker in the Turkish population
Beyaztas, Fatma Y.; Sezgin, Ilhan; Guz, Eylem; Erkol, Zerin (SAUDI MED J, 2007)Objective: To examine the allele frequencies of HumFABP(2) locus in 155 individuals from different regions of Turkey. Methods: The study was carried out in Cumhuriyet University Hospital, Sivas, Turkey, between March and ... -
ANGIOTENSIN CONVERTING ENZYME (ACE) GENE POLYMORPHISM AND BUERGER'S DISEASE
Ozen, Filiz; Kocak, Nadir; Ozdemir, Ozturk; Sezgin, Ilhan (JOHN WILEY & SONS INC, 2009)… -
Associations of fractalkine receptor (CX3CR1) and CCR5 gene variants with hypertension, diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis
Bagci, Binnur; Bagci, Gokhan; Huzmeli, Can; Sezgin, Ilhan; Ozdemir, Ozturk (SPRINGER, 2016)We aimed to investigate the associations of fractalkine receptor (CX3CR1) V249I, T280M and CCR5-59029 A/G gene polymorphisms in chronic renal failure (CRF) subjects undergoing hemodialysis and to evaluate possible associations ... -
CCR2 Polymorphism in Chronic Renal Failure Patients Requiring Long-Term Hemodialysis
Sezgin, Ilhan; Koksal, Binnur; Bagci, Gokhan; Kurtulgan, Hande Kucuk; Ozdemir, Ozturk (JAPAN SOC INTERNAL MEDICINE, 2011)Objective A number of chemokines and chemokine receptors are produced by intrinsic renal cells as well as by infiltrating cells during renal inflammation. The CCR2 chemokine receptor mediates leukocyte chemoattraction in ... -
Dental Findings in Cornelia De Lange Syndrome
Toker, Aslihan Soyal; Ay, Sinan; Yeler, Hasan; Sezgin, Ilhan (YONSEI UNIV COLL MEDICINE, 2009)Cornelia de Lange syndrome is a congenital disease, basically characterized by psychomotor retardation associated with a series of malformations, including mainly skeletal, craniofacial deformities together with gastrointestinal ... -
Frequency of familial Mediterranean fever (MEFV) gene mutations in patients with biopsy-proven primary glomerulonephritis
Huzmeli, Can; Candan, Ferhan; Bagci, Gokhan; Alaygut, Demet; Yilmaz, Ali; Gedikli, Asim; Bagci, Binnur; Timucin, Meryem; Sezgin, Ilhan; Kayatas, Mansur (SPRINGER LONDON LTD, 2017)Primary glomerulopathies are those disorders that affect glomerular structure, function, or both in the absence of a multisystem disorder. We aimed to evaluate the frequency of MEFV gene mutation to show possible coexistence ... -
Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers
Ozdemir, Ozturk; Sezgin, Ilhan; Kurtulgan, Hande Kucuk; Candan, Ferhan; Koksal, Binnur; Sumer, Haldun; Icagasioglu, Dilara; Uslu, Atilla; Yildiz, Fazilet; Arslan, Sulhattin; Cetinkaya, Selma; Citli, Senol; Oztemur, Zekeriya; Kayatas, Mansur (SPRINGER, 2011)The Familial Mediterranean Fever (FMF) shows an autosomal recessive pattern of inheritance and affects certain ethnic groups. Disease is caused by mutations in MEFV gene and more than 180 mutations have been defined in ... -
The protective effect of MCP-1-2518 A > G promoter polymorphism in Turkish chronic renal failure patients requiring long-term hemodialysis
Bagci, Binnur; Bagci, Gokhan; Candan, Ferhan; Ozdemir, Ozturk; Sezgin, Ilhan (SPRINGER, 2015)Monocyte chemoattractant protein-1 (MCP-1) plays a major role in the pathogenesis and progression of different types of human renal disease. Therefore, in this study, we aimed to investigate the effect of MCP-1 gene -2518 ... -
Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion
Kurtulgan, Hande Kucuk; Ozer, Leyla; Yildirim, Malik Ejder; Unsal, Evrim; Aktuna, Suleyman; Baltaci, Volkan; Akkus, Nejmiye; Sezgin, Ilhan (BIOMED CENTRAL LTD, 2015)Background: 14q duplications caused by parental pericentric inversion of chromosome 14 are rarely reported and no clear genotype-phenotype correlation has been determined yet. Case Presentation: Here we reported a 7 years ... -
Role of MTHFR gene polymorphisms, serum tissue inhibitor of metalloproteinases-1, thymus chemokine-1 and thrombospondin-1 in endometrial cancer
Yildirim, Malik Ejder; Kilicgun, Hasan; Kurtulgan, Hande Kucuk; Karakus, Savas; Ersan, Serpil; Bakir, Sevtap; Sezgin, Ilhan (E-CENTURY PUBLISHING CORP, 2016)The aim of this study was to evaluate the relationship between the MTHFR gene variants (677 C -> T and 1298 A -> C), serum tissue metalloproteinases inhibitor (TIMP-1), thrombospondin-1 (TSP-1), thymus chemokine-1 (TCK-1) ... -
The Role of the CCR2 Gene Polymorphism in Abdominal Aortic Aneurysms
Katrancioglu, Nurkay; Manduz, Sinasi; Karahan, Oguz; Yilmaz, Mehmet Birhan; Sezgin, Ilhan; Bagci, Gokhan; Berkan, Ocal (SAGE PUBLICATIONS INC, 2011)Objective: Chronic inflammation play an important role on abdominal aortic aneurysms (AAA) formation. Chemokine receptor-2 (CCR2) is involved in regulation of the inflammatory response. However, relation between CCR2 ... -
VEGF, sVEGFR-1 and Endostatin Serum Levels and VEGF Polymorphisms in Recurrent Aphthous Stomatitis
Yuce, Salim; Bagci, Binnur; Bagci, Gokhan; Dogan, Mansur; Koc, Sema; Sezgin, Ilhan; Candan, Ferhan; Uysal, Ismail Onder (DERMAN MEDICAL PUBL, 2016)Aim: Recurrent aphthous stomatitis (RAS) is one of the most frequent diseases of the oral mucosa, characterized by chronic, painful, recurrent, and necrotizing ulcerations. The precise etiology and pathogenesis of RAS have ...
