The frequency of Familial Mediterranean fever gene mutations and genotypes at Kirikkale and comparison with the mean of regional MEFV mutation frequency of …

DB Sayın Kocakap, A Günel-Özcan, F Cabuk… - Molecular biology …, 2014 - Springer
In this study we have retrospectively analysed the mutation spectrum of the 351 Familial
Mediterranean fever patients referred to Kırıkkale University Faculty of Medicine, Department of …

Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction

…, N Matevska, CM Lye, F Cabuk… - Nephrology Dialysis …, 2010 - academic.oup.com
Background. Congenital pelvi-ureteric junction obstruction (PUJO) affects 0.3% of human
births. It may result from aberrant smooth muscle development in the renal pelvis, resulting in …

Association of MTHFR A1298C polymorphism with conotruncal heart disease

BDS Kocakap, C Sanli, F Cabuk, M Koc… - Cardiology in the …, 2015 - cambridge.org
Congenital heart diseases are common congenital anomalies with 1% prevalence worldwide
and are associated with significant childhood morbidity and mortality. Among a wide range …

Tolmetin and salicylate therapy in acute rheumatic fever: Comparison of clinical efficacy and side‐effects

…, F Şenocak, B Öcal, CŞ Karakurt, F Çabuk - Pediatrics …, 2003 - Wiley Online Library
Background : The arthritis of rheumatic fever is very responsive to treatment with salicylates,
but there are many adverse reactions, especially hepatotoxicity, due to aspirin (…

[PDF][PDF] The association of paraoxonase 1 gene L55M polymorphism with the extent and severity of coronary artery disease in the Turkish population and its …

…, MT Doğru, V Şimşek, F Çabuk… - Anatolian Journal of …, 2016 - jag.journalagent.com
Objective: Coronary artery disease (CAD) is a common, complex, and progressive disorder
characterized by the accumulation of lipids and fibrous elements in the arteries. It is one of …

The prevalence of mental retardation by gender, age of diagnosis and location in Zonguldak province, Turkey

FN Ayoglu, F Cabuk, S Kiran, A Ocakci, Z Sahin… - Neurosciences …, 2008 - nsj.org.sa
OBJECTIVE: To evaluate the prevalence of mental retardation by gender, age of diagnosis,
and location in Zonguldak, Turkey. METHODS: The data of 1909 mentally retarded children …

TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy

F Çabuk, HG Karabulut, T Tuncali… - The Turkish journal of …, 2007 - turkjpediatr.org
Fallot tetralogy (FT) is the most frequently observed conotruncal heart defect (CTHD) and
accompanies 15% of the 22q11 deletion syndromes, DiGeorge/ velocardiofacial (DGS/VCFS) …

Varikoseli olan hastalarda Y kromozomu mikrodelesyonu-infertilite ilişkisi

…, A Dursun, Ç Yeşilli, İ Seçkiner, F Çabuk… - SDÜ Tıp Fakültesi …, 2006 - dergipark.org.tr
SüleymanDemirel Üniversitesi TIP FAKÜLTESİ DERGİSİ: 2007 Mart; 14(1) Varikoseli olan
hastalarda Y kromozomu mikrodelesyonu-infertilite ilişkisi Sevcan Bozdoğan*, Ahmet Dursun*…

Malformations due to warfarin: A case report

…, S Karademir, B Öcal, F Şenocak, F Çabuk… - International Journal of …, 2000 - Springer
We report a 5-month-old infant with severe growth retardation who was exposed to in utero
warfarin for the first 4 months. She had a dysmorphic face with depressed nasal hypoplasia …

< The> prevalence of mental retadation by gender, age of diagnosis and location in Zonguldak province, Turkey

A Ferruh N, C Feryal, K Sibel, O Ayse, S Zuhtu… - 2008 - pesquisa.bvsalud.org
To evaluate the prevalence of mental retardation by gender, age of diagnosis, and location
in Zonguldak, Turkey. The data of 1909 mentally retarded children recorded between 1995 …