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European Journal of Drug Metabolism and Pharmacokinetics|February 4, 2015
The CYP4502D6 *4 and *6 alleles are the molecular genetic markers for drug response: implications in colchicine non-responder FMF patientsSinem Yalcıntepe, Ozturk Ozdemır, Coskun Sılan, et al.
Nefrologia|September 24, 2021
A new technique for the detection of dry weight in hemodialysis patients: Estimated pulmonary capillary wedge pressure. A tissue Doppler imaging studyGürsel Yildiz, Ender Hur, Kemal Magden, et al.
Turkiye Parazitolojii Dergisi|May 2, 2007
[The incidence of Demodex folliculorum in patients with chronic kidney deficiency]Semra Ozçelik, Zeynep Sümer, Serpil Değerli, et al.
Nefrologia|December 2, 2022
A new technique for the detection of dry weight in hemodialysis patients: Estimated pulmonary capillary wedge pressure. A tissue Doppler imaging studyGürsel Yildiz, Ender Hur, Kemal Magden, et al.
Hemodialysis International. International Symposium on Home Hemodialysis|April 5, 2013
Evaluation of association between atherogenic index of plasma and intima-media thickness of the carotid artery for subclinic atherosclerosis in patients on maintenance hemodialysisGürsel Yildiz, Alptekin Duman, Hüseyin Aydin, et al.
Renal Failure|August 20, 2011
Association between ABCB1 (MDR1) gene 3435 C>T polymorphism and colchicine unresponsiveness of FMF patientsFiliz Ozen, Coskun Silan, Ahmet Uludag, et al.
Saudi Medical Journal|February 10, 2009
The risk factors for and prevalence of coronary artery disease in heavy vehicle driversLevent Ozdemir, Okan O Turgut, Seher Aslan, et al.
Endocrine Research|April 23, 2010
Inspiratory muscle strength is correlated with carnitine levels in type 2 diabetesFatih Kiliçli, Sebila Dökmetaş, Ferhan Candan, et al.
Renal Failure|November 15, 2014
Bcıı--RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysisOzturk Ozdemir, Mansur Kayatas, Selma Cetinkaya, et al.
Clinical Rheumatology|June 3, 2017
Frequency of familial Mediterranean fever (MEFV) gene mutations in patients with biopsy-proven primary glomerulonephritisCan Huzmeli, Ferhan Candan, Gokhan Bagci, et al.
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