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Toplam kayıt 172, listelenen: 91-100
Public'S Knowledge, Opinions And Behaviors About Crimean-Congo Hemorrhagic Fever: An Example From Turkey
(Kafkas Univ, Veteriner Fakultesi Dergisi, 2010)
The aim of this study was to determine the knowledge, opinions and behaviors of the adults, regarding Crimean-Congo Hemorrhagic Fever (CCHF). This descriptive study data was collected from 405 adults who attended two health ...
The Construct Validity and Reliability of the Turkish Version of Spreitzer'S Psychological Empowerment Scale
(2010)
Background Today, many organizations have adopted some kind of empowerment initiative for at least part of their workforce. Over the last two decades, two complementary perspectives on empowerment at work have emerged: ...
Mutations In Stat3 And Diagnostic Guidelines For Hyper-Ige Syndrome
(Mosby-Elsevier, 2010)
Background: The hyper-IgE syndrome (HIES) is a primary immunodeficiency characterized by infections of the lung and skin, elevated serum IgE, and involvement of the soft and bony tissues. Recently, HIES has been associated ...
Revisiting Human Il-12R Beta 1 Deficiency A Survey Of 141 Patients From 30 Countries
(Lippincott Williams & Wilkins, 2010)
Interleukin-12 receptor beta 1 (IL-12R beta 1) deficiency is the most common form of Mendelian susceptibility to mycobacterial disease (MSMD). We undertook an international survey of 141 patients from 102 kindreds in 30 ...
Mutations In The Gene Encoding The Rer Protein Fkbp65 Cause Autosomal-Recessive Osteogenesis Imperfecta
(Cell Press, 2010)
Osteogenesis imperfecta is a clinically and genetically heterogeneous brittle bone disorder that results from defects in the synthesis, structure, or posttranslational modification of type I procollagen. Dominant forms of ...
Mutations In Vipar Cause An Arthrogryposis, Renal Dysfunction And Cholestasis Syndrome Phenotype With Defects In Epithelial Polarization
(Nature Publishing Group, 2010)
Arthrogryposis, renal dysfunction and cholestasis syndrome (ARC) is a multisystem disorder associated with abnormalities in polarized liver and kidney cells. Mutations in VPS33B account for most cases of ARC. We identified ...
Mutations In Wdr62, Encoding A Centrosome-Associated Protein, Cause Microcephaly With Simplified Gyri And Abnormal Cortical Architecture
(2010)
Genes associated with human microcephaly, a condition characterized by a small brain, include critical regulators of proliferation, cell fate, and DNA repair. We describe a syndrome of congenital microcephaly and diverse ...
The Results Of Fetal Echocardiography In A Tertiary Center And Comparison Of Low- And High-Risk Pregnancies For Fetal Congenital Heart Defects
(Aves Yayincilik, 2010)
Objective: Fetal echocardiography (FE) is considered for fetal, maternal or hereditary reasons in pregnants with suspect of intrauterine heart disease (IUHD). However, in few studies it was reported that most of the fetuses ...
Identification Of Clinical And Simple Laboratory Variables Predicting Responsible Gastrointestinal Lesions In Patients With Iron Deficiency Anemia
(2010)
Iron deficiency anemia (IDA) is a frequent disorder. Also, it may be a sign of underlying serious diseases. Iron deficiency points to an occult or frank bleeding lesion when occurred in men or postmenopausal women. In this ...