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Toplam kayıt 798, listelenen: 1-10
Monitoring and prognostic evaluation of patients with congenital hypothyroidism treated in a pediatric endocrinology unit
(TURKISH J PEDIATRICS, 2013)
In this study, the etiological factors, diagnostic approaches, dose, and duration of treatment were compared between cases with transient and permanent congenital hypothyroidism (CH) with respect to prognosis. One hundred ...
Association of TRPM Channel Gene Polymorphisms with Systemic Sclerosis
(INT INST ANTICANCER RESEARCH, 2015)
Background/Aim: Systemic sclerosis (SSc) is an inflammatory disease characterized by vascular abnormalities and fibrosis. The aim of the present study was to investigate the possible role of transient receptor potential ...
Fournier's gangrene current approaches
(WILEY-BLACKWELL, 2016)
Fournier's gangrene is a rare but highlymortal infectious disease characterised by fulminant necrotising fasciitis involving the genital and perineal regions. The objective of this study is to analyse the demographics, ...
Prevalence of anticardiolipin antibodies in type 1 diabetes and autoimmune thyroiditis
(MEDYCYNA PRAKTYCZNA, 2010)
INTRODUCTION High levels of anticardiolipin (aCL) antibodies may predict vascular complications that could develop in type 1 diabetes and auto-immune thyroiditis (AIT). However, the clinical relevance of these antibodies ...
The New Anatomical Classification System for Orbital Exenteration Defect
(LIPPINCOTT WILLIAMS & WILKINS, 2017)
Background: The unique anatomy of the orbita and the different behavior of each malignant tumor cause us to perform the various types of orbital exenteration that yields to varying defect each ofwhich has own specific ...
Paraoxonase-1 192/55 Polymorphisms and the Risk of Lung Cancer in a Turkish Population
(INT INST ANTICANCER RESEARCH, 2011)
Aim: The purpose of the present study was to investigate the possible association of paraoxonase-1 (PON1) 192/55 polymorphisms with lung cancer (LC) risk in a Turkish population. Materials and Methods: A population-based, ...
11 beta-hydroxysteroid dehydrogenase type 1 gene expression is increased in ascending aorta tissue of metabolic syndrome patients with coronary artery disease
(FUNPEC-EDITORA, 2012)
11 beta-hydroxysteroid dehydrogenase type 1 (11 beta-HSD-1) activity and mRNA levels are increased in visceral and subcutaneous adipose tissues of metabolic syndrome subjects. We analyzed 11 beta-HSD-1 expression in human ...
PET-MRI Findings of Two Patients with Breast Carcinoma before Treatment
(AVES, 2016)
Integrated positron-emission tomography-magnetic resonance imaging (PET-MRI) is a new hybrid simultaneous imaging modality with higher soft tissue contrast and lower radiation doses compared with PET-CT. Two patients who ...
A Randomized, Double-blind, Placebo-controlled Study to Assess QTc Interval Prolongation of Standard Dose Aflibercept in Cancer Patients Treated With Docetaxel
(LIPPINCOTT WILLIAMS & WILKINS, 2013)
The effect of repeated doses of aflibercept on ventricular repolarization in cancer patients was evaluated in an intensive electrocardiogram trial. This randomized, placebo-controlled, double-blind trial was conducted in ...
Prenatal diagnosis of a digynic triploid fetus in the second trimester: transvaginal two-dimensional ultrasound, color Doppler and fetoplacental Doppler velocity waveform findings
(I R O G CANADA, INC, 2011)
Introduction: Triploidy in the second trimester is a sporadic, rare lethal chromosomal abnormality characterized by an extra haploid chromosome set (3n = 69). Doppler blood flow study in fetal triploidy syndrome is rarely ...