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The Nutritional Knowledge and Habits of Basketball Players In Elit Level
Emin SÜEL, İbrahim ŞAHİN, Mehmet Ali KARAKAYA, Yüksel SAVUCUPages: 271-275
The purpose of this study was to determine the nutritional knowledge and habits of basketball players in elite level. 32 female basketball players fro...
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An Investigation of the Levels of Antioxidants Vitamins ( A, E and C), Selenium in Serum and Glutathione Peroxidase (GSH-Px) in Erythrocytes of Goitre Patient's
Fikret KARATAŞ, Uğur AŞKIN, İhsan HALİFEOĞLU, Emir DÖNDERPages: 277-280
In this study, the antioxidant vitamin (A, E and C) and selenium levels in the serum and GSH-Px activity in erythrocytes of 66 patients with goitre a...
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Retrospective Analysis Of Patiens With Pelvic Fracture In Our Emergency Service
Mustafa YILDIZ, Alaattin GEDİKLİ, Polat DURUKAN, Mehmet BULUT, Yunsur ÇEVİK, Erhan YILMAZPages: 281-284
Although pelvic fractures are only 3% of all fractures; they are common and often devastating injuries. Along with a high mortality, the long-term mor...
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A Different Color Doppler Ultrasonography Sign In Diagnosis Of Urinary Stones: Twinkling Artifact
Mehmet Ruhi ONUR, Rahmi ONURPages: 285-288
A Different Color Doppler Ultrasonography (US) finding In Diagnosis Of Urinary Stones: Twinkling Artifact The purpose of this study was to determine ...
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Peripheral Blood Cytogenetic Analysis and Clinical Evaluation of Down Syndrome Cases Determined by Medical Biology and Genetic Department of Medical Faculty in Firat University in Term of 2000-2005
Hüseyin YÜCE, Ülkü ÖZBEY, Deniz EROL, Ebru ETEM, Şükriye Derya DEVECİ, Gülay GÜLEÇ CEYLAN, Murat KARA, Halit ELYASPages: 289-291
Trisomies occur in the result of ‘'meiotic non-disjunction'' during gametogenesis. In humans, trisomy 21 or Down Syndrome is the best known and the mo...
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Cytogenetic analysis of mental retarded children in Elazig region
Ülkü ÖZBEY, Hüseyin YÜCE, Murat KARA, Nimet KABAKUŞ, Halit ELYASPages: 293-296
Fragile X syndrome is the most common cause of hereditary mental retardation (MR) in humans. It is the second reason of hereditary and non hereditary ...
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Effects of Egb-761 in Rats with Obstructive Jaundice
Saim BERCIN, Ziya CETINKAYA, Yasemin BULUT, Nusret AKPOLAT, Erhan AYGENPages: 297-301
The aim of this study was to investigate the effects of ginkgo biloba extract (EGb-761) on liver and terminal ileum morphology, biochemical parameters...
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Investigation of Mitochodrial DNA deletions in Oligoasthenospermic Infertile Patients with and without Varicocele
Arslan ARDIÇOĞLU, Faruk KUYUCU, Ebru ETEM, M.Kemal ATİKELER, İmed DUKSAL, Ömer Ali UYAR, Hüseyin YücePages: 303-306
The most common cause of male infertility is varicocele. In the present study we aimed to investigate the mitochondrial deletions in the control ferti...
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Paraoxonase and Arylesterase Levels in Behçet's Disease
Ahmet IŞIK, Bilal ÜSTÜNDAĞPages: 307-315
Lipid hydroperoxides (LOOHs) are by product of lipid peroxidation. Paraoxonase (PON), arylesterase (ARE), free sulphydryl (SH) groups and ceruloplasmi...
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A Patient with Blastocystis hominis in Emergency Department: A case report
Salih KUK, Mustafa YILDIZ, Mehmet Nuri BOZDEMİR, Mustafa BAŞTÜRK, Ahmet ERENSOYPages: 317-319
Blastocystis hominis is one of the most common parasites found in the human intestinal tract. This organism was considered a harmless over the years. ...
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Marshall Syndrome; Case Report
A.Neşe ÇITAK KURT, Saadet AKARSU, Abdullah KURT, Erdal YILMAZ, Feyza İNCEKÖY GİRGİN, A. Denizmen AYGÜNPages: 321-322
Marshall is a autosomal dominant transition sendrom which seen rarely, characterized with craniofacial abnormalities, deafness, oculer defects, skelet...
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Eruptive Vellus Hair Cyst (Case Report)
Perihan ÖZTÜRK, Arzu ATASEVEN, Ferda DAĞLIPages: 323-325
Eruptive vellus hair cyst (EVHC) are formed as a result of faulty development or defective formation of vellus type hair follicles. Usually the lesion...
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Intracranial Hemorrhage Due To Vitamin K Deficiency In An Infant Despite Prophylaxis At Birth
Kaan DEMİRÖREN, Haluk YAVUZ, Saadet DEMİRÖRENPages: 327-329
Vitamin K deficiency bleeding is rare in infants who received vitamin K prophylaxis at birth. We present a case of a 7-week-old infant with intracrani...