Browsing by Author "Kockara, Ayse Seker"
Now showing items 1-4 of 4
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Evaluation of 61 Secondary Amyloidosis Patients: A Single-Center Experience from Turkey
Huzmeli, Can; Candan, Ferhan; Bagci, Gokhan; Alaygut, Demet; Bagci, Binnur; Yildiz, Esin; Kockara, Ayse Seker; Kayatas, Mansur (DERMAN MEDICAL PUBL, 2016)Aim: To evaluate demographic,clinical and laboratory characteristics. causes, MEFV gene mutations, and mortality rates of patients with secondary amyloidosis. Material and Method: 61 patients who had been diagnosed with ... -
Gitelman's syndrome associated with chondrocalcinosis: a case report
Kockara, Ayse Seker; Candan, Ferhan; Huzmeli, Can; Kayatas, Mansur; Alaygut, Demet (INFORMA HEALTHCARE, 2013)Gitelman's syndrome (GS) is a rare disease with autosomal recessive trait, characterized by hypokalemia, hypomagnesemia, metabolic alkalosis, hypocalciuria and hyperkinemic hyperaldosteronism. While muscle weakness, tetany, ... -
Upper extremity venous thrombosis associated with primary antiphospholipid syndrome and immunoglobulin M nephropathy in diabetes mellitus type II
Huzmeli, Can; Candan, Ferhan; Kockara, Ayse Seker; Alaygut, Demet; Kayatas, Mansur (AVES, 2018)Antiphospholipid syndrome (APS) is a disorder characterized by antiphospholipid antibody positivity, arterial or venous thrombosis, and fetal loss. In APS, renal as well as vascular and glomerular involvement is observed. ...