Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sakir Özgür Keskek"'
Autor:
Sakir Özgür Keskek, Filiz Eksi Haydardedeoglu, Sinan Kırım, Serap Angay, Gülay Ortoglu, Mehmet Tasdemir, Adil Karaca, Yoel Toledano, Tayyibe Saler
Publikováno v:
QScience Connect, Vol 2013, Iss 1 (2013)
Background: Depression and obesity are common disorders. Obesity is also predictive of several chronic diseases like hypertension and diabetes. The aim of this study was to evaluate and compare depression frequency of obese patients with hypertension
Externí odkaz:
https://doaj.org/article/01dd43b5f4bb42e9ab6ccdcc44f576a3
Publikováno v:
Haseki Tıp Bülteni, Vol 59, Iss 4, Pp 340-344 (2021)
Aim:Uncontrolled diabetes can lead to complications which are related to high blood sugar and insulin resistance (IR). A decrease in serum magnesium (Mg) levels can cause an increase in IR and a worsening of glycaemic control. In this study, we aimed
Externí odkaz:
https://doaj.org/article/30dbca9f4bab42e0a7d231e6f551f826
Autor:
Sema Kunt, Şakir Özgür Keşkek
Publikováno v:
Haseki Tıp Bülteni, Vol 58, Iss 3, Pp 240-244 (2020)
Aim:The aim of this study was to investigate the level of visceral adiposity index (VAI), body fat index and fat mass in patients with chronic renal failure (CRF).Methods:A total of 231 subjects were enrolled, of which 83, 64 and 84 subjects were hem
Externí odkaz:
https://doaj.org/article/9f9ec72597794f2795db02727dc16227
Publikováno v:
Annals of Saudi Medicine, Vol 36, Iss 6, Pp 409-413 (2016)
BACKGROUND: Normative optical coherence tomography (OCT) data is required for different subsets of the population as ethnic differences in retinal nerve fiber layer (RNFL) thickness have been reported. An OCT database for the normal Turkish populatio
Externí odkaz:
https://doaj.org/article/386db06c95964936a2e014982ab3a795
Publikováno v:
Haseki Tıp Bülteni, Vol 52, Iss 1, Pp 64-66 (2014)
Wilson’s disease is a rare autosomal recessive inherited disorder of copper metabolism that causes various degrees of hepatic and neuropsychiatric symptoms. The condition is due to mutations in the ATP7B gene localized to arm 13q. The clinical sign
Externí odkaz:
https://doaj.org/article/e1461a15f70743f281d813dec28e1de9
Publikováno v:
Turkish Archives of Otorhinolaryngology, Vol 47, Iss 1, Pp 53-57 (2009)
Retropharyngeal, parapharyngeal hematomas are rare but potentially life-threatening conditions that require a prompt diagnosis. Most of the pharyngeal space hematomas described in the literature are associated with complicating factors such as tumour
Externí odkaz:
https://doaj.org/article/d95a3f230dd145118baa646aaa996f24
Autor:
Nedime Sahinoglu-Keşkek, Gokhan Soker, Şakir Özgür Keşkek, Sehire Sahinoglu, Figen Unal, Fikret Unal, Selim Cevher
Publikováno v:
Case Reports in Ophthalmological Medicine, Vol 2015 (2015)
Objective. Meningiomas are benign primary meningeal tumors and are seen rare in children and adolescents. Clinical Presentation and Intervention. A 15-year-old Turkish boy reported a 1-month history of headache and blurred vision in both eyes. His vi
Externí odkaz:
https://doaj.org/article/16e7166b8937461caeb44af32a1d46dc
Publikováno v:
Advances in Hematology, Vol 2014 (2014)
Background. The aim of this study was to investigate the association between iron deficiency anemia and H. pylori in patients with normal gastrointestinal tract endoscopy results. Materials and Methods. A total of 117 male patients with normal gastro
Externí odkaz:
https://doaj.org/article/191bbc37b9704248b8d880ed263adb7f
Publikováno v:
Archives of Endocrinology and Metabolism, Iss 0
ABSTRACT Objective: Polycystic ovary syndrome (PCOS) is a common endocrine disorder in women of reproductive age. The renal resistive index (RRI) is a measure of renal arterial resistance to blood flow. The aim of this study was to investigate the re
Externí odkaz:
https://doaj.org/article/3d597b003432425eb1228075064a2b4e