Browsing by Author "Kayatas M."
Now showing items 1-4 of 4
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C3 mesangial proliferative glomerulonephritis initially presenting with atypical hemolytic uremic syndrome: A case report
Huzmeli C.; Candan F.; Seker A.; Yildiz E.; Terzi H.; Kayatas M. (2016)Background: Hemolytic uremic syndrome is characterized by acute renal failure, thrombocytopenia, and Coombs-negative hemolytic anemia. In C3 mesangial proliferative glomerulonephritis, an increase in mesangial cell ... -
Evaluation of 61 secondary amyloidosis patients: A single-center experience from turkey [61 Sekonder amiloidoz hastasının değerlendirilmesi: Türkiyeden tek merkez deneyimi]
Huzmeli C.; Candan F.; Bagci G.; Alaygut D.; Bagci B.; Yildiz E.; Kockara A.S.; Kayatas M. (2016)Aim: To evaluate demographic,clinical and laboratory characteristics, causes, MEFV gene mutations, and mortality rates of patients with secondary amy-loidosis. Material and Method: 61 patients who had been diagnosed with ... -
IgA nephropathy: A rare lesion in renal biopsy in systemic lupus erythematosus: Case reports and review of literature
Yildiz G.; Cicekli E.; Kayatas M.; Yilmaz A.; Candan F. (2013)Lupus nephritis is an infl ammation of the kidney caused by systemic lupus erythematosus (SLE). Lupus nephritis is a frequent complication of SLE that increases mortality and morbidity. Minimal glomerular lesions, mesangial ... -
Variable R.Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677Tgene polymorphism: From genetics to epigenetics
Ozdemir O.; Silan F.; Urfali U.; Uludag A.; Ari E.; Kayatas M. (2014)The role of inflammation, hyperhomocysteinemia, germ-line genetic markers and epimutations haven't been understood completely in chronic renal failure (CRF). DNA methylation is a postreplicative modification mechanism that ...