Başlık için Temel Tıp Bilimleri Bölümü Makale Koleksiyonu listeleme
Toplam kayıt 459, listelenen: 186-205
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Evaluation Of Diagnostic Tests Using Information Theory For Multi-Class Diagnostic Problems And Its Application For The Detection Of Occlusal Caries Lesions
(Galenos Yayıncılık, 2014)Background: Several methods are available to evaluate the performance of the tests when the purpose of the diagnostic test is to discriminate between two possible disease states. However multi-class diagnostic problems ... -
Evaluation Of Outer Hair Cell Function And Medial Olivocochlear Efferent System In Patients With Type Ii Diabetes Mellitus
(Tubitak Scientific & Technical Research Council Turkey, 2014)Aim: This study was designed to investigate the function of outer hair cells and medial olivocochlear efferents in type II diabetes mellitus (DM). Materials and methods: There were 50 patients with type II DM and 51 age-and ... -
Evaluation Of Risk Factors Affecting Substance Use Among Tenth-Grade Students
(2018)Aim The aim of this study is to detect the prevalence of substance use among tenth-grade students; their thoughts, attitudes, behaviors, and tendencies towards substance use; and risk factors of substance use in tenth-grade ... -
Evidence For The Control Of Aggrecanases By Insulin And Glucose In Alzheimer'S Disease
(Kure Iletisim Grubu A S, 2014)Objective: Alzheimer's disease (AD) is a progressive and irreversible central nervous system disease, which slowly destroys cognitive skills and memory, and eventually even the ability to handle the simplest tasks. The ... -
Examination Of Inequality Of Life Span By Using The Gini Coefficient In The Turkish Population For The Period 1990-2008
(Aves Yayincilik, 2011)Objective: The aim of this study is to show that the Gini coefficient used in economics, particularly in exposing inequality in income levels can also be used in the field of health, especially for measuring inequality ... -
Exome Sequencing Reveals Cubilin Mutation As A Single-Gene Cause Of Proteinuria
(Amer Soc Nephrology, 2011)In two siblings of consanguineous parents with intermittent nephrotic-range proteinuria, we identified a homozygous deleterious frameshift mutation in the gene CUBN, which encodes cubulin, using exome capture and massively ... -
Factors Affecting The Etiology Of Intractable Pruritus In Hospitalized Patients Without Primary Skin Lesions
(2019)Introduction: Pruritus is a common symptom that has dermatologic, systemic, neurological, psychogenic, mixed, and unknown causes. The aim of this study was to identify the underlying origin of pruritus (UOP) in hospitalized ... -
Fibroblastic Reticular Cells And Fibroblast-Like Cells Determined By Monoclonal Antibodies B-F45 And B-D46 In Humans
(Saudi Med J, 2004)Objective: Identification of stromal microenvironmental components of lymphoid organs is relatively harder at light microscopic level as few markers, which are mostly not very specific, are available to be used for such a ... -
Four Novel Thymidine Phosphorylase Gene Mutations In Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome (Mngie) Patients
(Nature Publishing Group, 2003)Mitochondrial neurogastrointestinal encephalomyopathy syndrome (MNGIE) is a rare autosomal recessive neurologic disorder characterised by multiple mitochondrial DNA deletions. In this study, five Turkish IVINGIE patients ... -
Functional Mri Compliance In Children With Attention Deficit Hyperactivity Disorder
(Aves, 2015)PURPOSE We aimed to test the effect of prescan training and orientation in functional magnetic resonance imaging (fMRI) in children with attention deficit hyperactivity disorder (ADHD) and to investigate whether fMRI ... -
Genetic Analysis Of Chst6 And Tgfbi In Turkish Patients With Corneal Dystrophies: Five Novel Variations In Chst6
(2016)Purpose To identify pathogenic variations in carbohydrate sulfotransferase 6 (CHST6) and transforming growth factor, beta-induced (TGFBI) genes in Turkish patients with corneal dystrophy (CD). Methods In this study, patients ... -
Genetic Polymorphism Of Manganese Superoxide Dismutase In Behcet'S Disease
(Turkish League Against Rheumatism, 2016)Objectives: This study aims to investigate the genetic association between single nucleotide mutation in mitochondrial manganese superoxide dismutase and a Behcet's disease (BD) population by using molecular techniques. ...