Browsing by Author "Alaygut, Demet"
Now showing items 1-16 of 16
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A 5-Year-Old Boy with Vomiting, Abdominal Pain, and Fatigue
Alaygut, Demet; Kilic, Suar Caki (SLACK INC, 2014)… -
Acute Colchicine Intoxication Complicated With Extramedullary Hematopoiesis Due to Filgrastim in a Child
Kilic, Suar C.; Alaygut, Demet; Unal, Ekrem; Koc, Elif; Patiroglu, Turkan (LIPPINCOTT WILLIAMS & WILKINS, 2014)Colchicine is a widely used alkaloid extract in children and adults for standard therapy and prophylaxis for amyloid deposition in different rheumatologic disorders. Colchicine intoxication is a rare but severe complication. ... -
An Adolescent Girl with an Abdominal Mass
Alaygut, Demet; Sezer, Ferhat; Guney, Cengiz; Kilic, Suar Caki; Solak, Orhan (MOSBY-ELSEVIER, 2014)… -
Assessment of 17 Pediatric Cases With Colchicine Poisoning in a 2-Year Period
Alaygut, Demet; Kilic, Suar Caki; Kaya, Ali; Oflaz, Mehmet Burhan; Bolat, Fatih; Cevit, Omer; Icagasioglu, Fusun Dilara (LIPPINCOTT WILLIAMS & WILKINS, 2016)Aim The aim of the study is to discuss clinical effects, treatments, and outcomes of pediatric colchicine poisoning. Method This study was designed as an observational case series study. The medical records of children ... -
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 ... -
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 ... -
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, ... -
Neutrophil-lymphocyte ratio in children with familial Mediterranean fever: Original article
Duksal, Fatma; Alaygut, Demet; Guven, Ahmet Sami; Ekici, Mahmut; Oflaz, Mehmet Burhan; Tuncer, Rukiye; Cevit, Omer (AVES, 2015)Objective: The aim of present study was (a) to evaluate the relationship between the neutrophil/lymphocyte (N/L) ratio and mutation types of familial Mediterranean fever (FMF) in children and (b) to evaluate the relationship ... -
Noninvasive evaluation of cardiac autonomic modulation in children with primary Raynaud's phenomenon: a controlled study
Oflaz, Mehmet Burhan; Ece, Ibrahim; Kibar, Ayse Esin; Balli, Sevket; Alaygut, Demet; Guven, Ahmet Sami; Bolat, Fatih; Duksal, Fatma; Cevit, Omer (SPRINGER LONDON LTD, 2014)This study aimed to objectively evaluate autonomic nervous function in children with primary Raynaud's phenomenon (PRP). Thirty-two children with PRP and 30 healthy subjects were included in the study. We analyzed heart ... -
Pasteurella aerogenes as an Asymptomatic Bacteriuria Agent
Alaygut, Demet; Engin, Aynur (OXFORD UNIV PRESS, 2018)'Asymptomatic bacteriuria' (ASB) is isolation of a specified quantitative count of bacteria in an appropriately collected urine specimen obtained from a person without symptoms or signs referable to urinary infection. ... -
Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of Turkey
Huzmeli, Can; Candan, Ferhan; Alaygut, Demet; Bagci, Gokhan; Akkaya, Lale; Bagci, Binnur; Sozmen, Eser Yildirim; Kurtulgan, Hande Kucuk; Kayatas, Mansur (SPRINGER/PLENUM PUBLISHERS, 2016)Fabry disease (FD) is a progressive, X-linked inherited disorder of glycosphingolipid metabolism due to deficient or absent lysosomal alpha-galactosidase A (AGALA) activity. FD and familial Mediterranean fever (FMF) have ... -
The relationship between restless leg syndrome and 25-hydroxy D vitamin in hemodialysis patients
Huzmeli, Can; Candan, Ferhan; Timucin, Meryem; Alaygut, Demet; Akkaya, Lale; Seker, Ayse; Kayatas, Mansur (DERMAN MEDICAL PUBL, 2018)Aim: The purpose is to evaluate the relationship between Restless legs syndrome (RLS) and 25-Hydroxy D [25 (OH) D] vitamin level among hemodialysis patients. Material and Method: Hemodialysis patients, in Cumhuriyet ... -
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. ... -
What Is the Safe Approach for Neonatal Hypernatremic Dehydration? A Retrospective Study From a Neonatal Intensive Care Unit
Bolat, Fatih; Oflaz, Mehmet Burhan; Guven, Ahmet Sami; Ozdemir, Goktug; Alaygut, Demet; Dogan, Melih Timucin; Icagastoglu, Fusun Dilara; Cevit, Omer; Gultekin, Asim (LIPPINCOTT WILLIAMS & WILKINS, 2013)Objectives: The aims of this study were to evaluate the prevalence, complications, and mortality of hypernatremic dehydration in neonates and to compare the effect of correction rate at 48 hours on mortality and on ...