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The association of Visfatin levels with metabolic parameters and inflammation in diabetic nephropathy

GÜRSU, Meltem; Ozturk, Savaş; Behlul, Ahmet; Sumnu, Abdullah; Sakin, Abdullah; Sakin, Ayşegül; Sahin, Suleyman (2020)

© 2020, Yuzuncu Yil Universitesi Tip Fakultesi. All rights reserved.To investigate the visfatin levels at the stages of diabetic nephropathy(DNP), changes in visfatin levels according to stages of DNP, and the association ...

The Effect of Autosomal Dominant Polycystic Kidney Disease on Spirometric Parameters

Cakmak, Gulfidan; Ozturk, Savaş; GÜRSU, Meltem; Doner, Baris; Karaali, Zeynep; Sari, Mustafa; Sumnu, Abdullah; Ozler, Tuba Elif; Karandere, Faruk; Cebeci, Egemen (2020)

Aim: There is no enough data on pulmonary involvement in autosomal dominant polycystic kidney disease (ADPKD). The aim of this study is to examine pulmonary function test in patients with ADPKD with varying stages of renal ...

Is Pentraxin-3 a Stronger Marker of Inflammation than C-Reactive Protein in Chronic Kidney Disease?

Sumnu, Abdullah; Kazancioglu, Rumeyza; Koldas, Macit; Cebeci, Egemen; Ozkan, Oktay; Gursu, Meltem; Aydin, Zeki; Ozturk, Savaş; Karadag, Serhat; Uzun, Sami; Erdogan, Yasemin Doventas (2014)

OBJECTIVE : Pentraxin-3 (PTX-3) is elevated in uremic patients and related with albuminuria and endothelial dysfunction. We aimed to clarify the relationship of PTX-3 with inflammatory markers (hsCRP and IL-6) in patients ...

Paroxysmal Nocturnal Hemoglobinuria and Acute Kidney Injury: A Case Report

Ozturk, Savaş; KAZANCIOĞLU, Rümeyza; Gursu, Meltem; Cebeci, Egemen; Kilicarslan, Isin; Sumnu, Abdullah; Donmez, Halil (2013)

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare cause of hemolytic anemia. The major outlines of clinical presentation comprises findings of hemolysis, venous thrombosis and findings of bone marrow failure. The ...

Pseudoephedrine-induced Ventricular Tachycardia

Kumbasar, B.; KAZANCIOĞLU, Rümeyza; Ozturk, Savaş; Tahmaz, Meryem

Here, we report an unusual cause of ventricular tachycardia which had developed following pseudoephedrine intake. A 55 year old male patient was admitted to the emergency department with complaints of sustained palpitation. ...

Antierythropoietin Antibodies in Hemodialysis Patients Treated with Recombinant Erythropoietin

Gumus, Alper; Duz, Muhammet Emin; Memili, Vecihi; Ozturk, Savaş; KAZANCIOĞLU, Rümeyza; Koldas, Macit; Cebeci, Egemen (2014)

OBJECTIVE: Erythropoietin resistance is a serious problem in patients treated with recombinant erythropoietin. Antierythropoietin antibodies are considered to be one of the causes of this resistance.

NOONAN SENDROMU’NUN PRENATAL TANISINDA PTPN11 GEN ANALİZLERİNİN ETKİNLİĞİ

Kalelioğlu, İbrahim Halil; Başaran, Seher; Uyguner, Zehra Oya; Yüksel, Atıl; Has, Recep; Toksoy, Güven; Tepgeç, Fatih; Saraç Sivrikoz, Tuğba; Demir, Selma (2021)

Amaç: Hücre büyüme, farklılaşma, yaşlanma ve siklus düzenlenmesindeönemli rol oynayan RAS-MAPK (Rat-sarcoma-Mitogen-activated-protein-kinase) yolağında bulunan 29 gendeki dominantpatojenik varyantların yol açtığı klinik ...

The right temporal variant of frontotemporal dementia is not genetically sporadic: A case series

Barkhof, Frederik; van der Flier, Wiesje M.; Erkoyun, Hulya Ulugut; van der Lee, Sven J.; Nijmeijer, Bas; van Spaendonk, Rosalina; Nelissen, Anne; Scarioni, Marta; Dijkstra, Anke; Samancı, Bedia; GÜRVİT, İbrahim Hakan; Yıldırım, Zerrin; Tepgeç, Fatih; Bilgic, Basar; Rozemuller, Annemieke; Pijnenburg, Yolande; Cohn-Hokke, Petra; Scheltens, Philip (2021)

© 2021 - IOS Press. All rights reserved.Background: Right temporal variant frontotemporal dementia (rtvFTD) has been generally considered as a right sided variant of semantic variant primary progressive aphasia (svPPA), ...

Design and characterisation of colloidal nanocarriers for enhanced skin delivery of etodolac

Kahraman, Emine; GÜNGÖR, Sevgi; Saribey, Güler; ERDAL, Meryem Sedef (2021)

© 2021 Marmara University Press.The aim of this work was to develop colloidal nanocarriers for skin delivery of etodolac (ETD), which is a non-steroidal anti-inflammatory drug orally used for the management of acute pain ...

A rare urea cycle disorder in a neonate: N-acetylglutamate synthetase deficiency

BİBEROĞLU, GÜRSEL; Kesici, Selman; Ozyazici, Ahmet; Haberle, Johannes; Karaca, Meryem; Olgac, Asburce; Kasapkara, Cigdem S.; Kilic, Mustafa; Derinkuyu, Betul Emine; Azapagasi, Ebru (2020)

Urea cycle disorders (UCD), are genetically inherited diseases that may have a poor outcome due to to profound hyperammonemia. We report the case of a baby girl diagnosed as N-acetylglutamate synthase (NAGS) deficiency. ...