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Toplam kayıt 30, listelenen: 21-30
Kleptomania in Patients with Neuro-Behcet's Disease
(KARGER, 2013)
Objective: This study was conducted to characterize the prevalence and clinical features of kleptomania, an impulse control disorder, in patients with Behcet's disease involving the central nervous system. Subjects and ...
Interobserver variability in cervical smears from patients with a history of abnormal cytology: comparison of conventional pap smears and liquid-based cytology
(Erciyes Üniversitesi, Tıp Fakültesi, 2013)
Objective: One of the problems encountered when assessing cervical precancerous lesions is intra- and interobserver variability. The aim of this study was to determine the degree of interobserver variation in conventional ...
The effect of beta-aminopropionitrile and prednisolone on the prevention of fibrosis in alkali esophageal burns: an experimental study
(Hindawi Publishing Corporation, 2013)
Objective. The aim of this study was to investigate the efficacy of beta-aminopropionitrile (BAPN) and prednisolone on the prevention of esophageal damage and stricture formation after caustic esophageal burn. Method. ...
Determining the Awareness of and Compliance with Breast Cancer Screening among Turkish Residential Women
(ASIAN PACIFIC ORGANIZATION CANCER PREVENTION, 2013)
Background: Breast cancer is the leading cause of cancer-related deaths in women. Despite being associated with high morbidity and mortality, breast cancer is a disease that can be diagnosed and treated early. Materials ...
Impairment of BRCA1-Related DNA Double-Strand Break Repair Leads to Ovarian Aging in Mice and Humans
(AMER ASSOC ADVANCEMENT SCIENCE, 2013)
The underlying mechanism behind age-induced wastage of the human ovarian follicle reserve is unknown. We identify impaired ATM (ataxia-telangiectasia mutated)-mediated DNA double-strand break (DSB) repair as a cause of ...
Mitochondrial carrier homolog 1 (Mtch1) antibodies in neuro-Behcet's disease
(ELSEVIER SCIENCE BV, 2013)
Efforts for the identification of diagnostic autoantibodies for neuro-Behcet's disease (NBD) have failed. Screening of NBD patients' sera with protein macroarray identified mitochondrial carrier homolog 1 (Mtch1), an ...
Inherited platelet disorders including Glanzmann thrombasthenia and Bernard-Soulier syndrome
(AMER SOC HEMATOLOGY, 2013)
Inherited platelet disorders (IPDs) are a heterogeneous group of diseases affecting platelet production, morphology, and function. The degree of thrombocytopenia and functional abnormality of platelets determines the ...
Two-directional intercoronary communication: visualization of a very rare coronary anomaly and cause of ischemia
(CHINESE MEDICAL ASSOC, 2013)
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OPN gene polymorphism (Ala250) and lower serum OPN levels are associated with urolithiasis
(TAYLOR & FRANCIS LTD, 2013)
Osteopontin (OPN) is one of the urinary proteins with an important role in stone formation. Recently, OPN Ala250 (rs1126616) polymorphism and other single nucleotide polymorphisms (SNPs) have been studied to define their ...
Newborn Screening for Congenital Hypothyroidism
(GALENOS YAYINCILIK, 2013)
Newborn screening (NS) for congenital hypothyroidism (CH) is one of the major achievements in preventive medicine. Most neonates born with CH have normal appearance and no detectable physical signs. Hypothyroidism in the ...