Tür "info:eu-repo/semantics/article" Tıp Fakültesi için listeleme
Toplam kayıt 3962, listelenen: 61-80
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A Comparison of Pcr Detection of Meca With Oxacillin Disk Susceptibility Testing in Different Media and Sceptor Automated System for Both Staphylococcus Aureus and Coagulase-Negative Staphylococci Isolates
(Medknow Publications, 2008)Purpose: To evaluate three methods for 406 isolates of Staphylococcus aureus and coagulase-negative staphylococci (CNS) for the detection of methicillin resistance (MR) using National Committee for Clinical Laboratory ... -
A Comparison of Results of 3-Dimensional Gait Analysis and Observational Gait Analysis in Patients With Knee Osteoarthritis
(Turkish Assoc Orthopaedics Traumatology, 2015)Objective: This study aimed to investigate levels of validity, and inter- and intra-observer reliability of observational gait analysis (OGA) in clinical usage, done by the physical therapists with varying clinical experience, ... -
A Comparison of the Acute Effects of Radial Extracorporeal Shockwave Therapy, Ultrasound Therapy, and Exercise Therapy in Plantar Fasciitis
(2018)This study was conducted to compare the acute effects of radial extracorporeal shockwave therapy (r-ESWT), ultrasound (US) therapy and home exercise therapy on pain, fatigue, performance and walking distance in women with ... -
A Comparison of the Effects of Platelet-Rich Plasma and Demineralized Bone Matrix on Critical Bone Defects: An Experimental Study on Rats
(Turkish Assoc Trauma Emergency Surgery, 2017)BACKGROUND: Delayed union of fractured bone is one of the main problems of orthopedics and traumatology practice. It was hypothesized that the beneficial effects of allogeneic platelet-rich plasma (PRP) would be valuable ... -
A Comparison Of Three-Dimensional And Two-Dimensional Cephalometric Evaluations Of Children With Cleft Lip And Palate
(2011)Objectives: The aim of this retrospective study was to compare the consistency of orthodontic measurement performed on cephalometric films and 3D CT images of cleft lip and palate (CLP) patients. Methods: The study was ... -
A Complex Splicing Defect Associated With Homozygous Ankyrin-Deficient Hereditary Spherocytosis
(Amer Soc Hematology, 2007)Defects in erythrocyte ankyrin are the most common cause of typical, dominant hereditary spherocytosis (HS). Detection of ankyrin gene mutations has been complicated by allelic heterogeneity, large gene size, frequent de ... -
A Comprehensive Framework Identifying Readmission Risk Factors Using The Chaid Algorithm: A Prospective Cohort Study
(Oxford Univ Press, 2018)Objective: To identify frequency of readmission after discharge from internal-medicine wards, readmission risk factors, and reasons and costs of readmission. Design: Prospective cohort study. Setting: A tertiary-care ... -
A Comprehensive Molecular Study on Coffin-Siris And Nicolaides-Baraitser Syndromes Identifies A Broad Molecular and Clinical Spectrum Converging on Altered Chromatin Remodeling
(Oxford Univ Press, 2013)Chromatin remodeling complexes are known to modify chemical marks on histones or to induce conformational changes in the chromatin in order to regulate transcription. Denovodominant mutations in different members of the ... -
A Comprehensive Simulation Study On Classification Of Rna-Seq Data
(2017)RNA sequencing (RNA-Seq) is a powerful technique for the gene-expression profiling of organisms that uses the capabilities of next-generation sequencing technologies. Developing gene-expression-based classification algorithms ... -
A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused By Defective De Novo Phosphatidylcholine Biosynthesis
(Cell Press, 2011)Congenital muscular dystrophy is a heterogeneous group of inherited muscle diseases characterized clinically by muscle weakness and hypotonia in early infancy. A number of genes harboring causative mutations have been ... -
A Cross Section of Autosomal Recessive Limb-Girdle Muscular Dystrophies In 38 Families
(BMJ, 2000)Limb-girdle muscular dystrophies constitute a broad range of clinical and genetic entities. We have evaluated 38 autosomal recessive limb-girdle muscular dystrophy (LGMD2) families by linkage analysis for the known loci ... -
A Cross-Over Medication Trial For Patients With Autosomal-Dominant Hypertension With Brachydactyly
(Blackwell Science Inc, 1998)We examined a family with autosomal-dominant hypertension and brachydactyly from northeastern Turkey. The hypertension was defined as severe, resulting in stroke before age 50 years, featuring normal renin, aldosterone, ... -
A Cross-Sectional Study Investigating Association Of Liver Diseases In Moderate To Severe Psoriasis Patients
(2019)Background and Design: Non-alcoholic fatty liver disease (NAFLD), which is a systemic comorbidity of psoriasis, is the most common liver disease in population with risk of cirrhosis progression. The aim of this study was ... -
A Current Analysis Of Caregivers' Approaches To Fever And Antipyretic Usage
(J Infection Developing Countries, 2014)Introduction: The aim of this survey was to investigate the current knowledge, attitudes, and practices of febrile children's caregivers about fever, antipyretic usage, and temperature measurement methods in a tertiary ... -
A Demineralized Calf Vertebra Model As An Alternative To Classic Osteoporotic Vertebra Models For Pedicle Screw Pullout Studies
(Springer, 2008)Screws, clamps and other spinal instrumentation materials are tested using healthy animal and healthy human vertebrae, but the application of similar tests to an osteoporotic vertebra is generally neglected because of high ... -
A Diagnosis to Consider in An Adult Patient With Facial Features And Intellectual Disability: Williams Syndrome
(2017)Williams syndrome (OMIM #194050) is a rare, well-recognized, multisystemic genetic condition affecting approximately 1/7,500 individuals. There are no marked regional differences in the incidence of Williams syndrome. The ... -
A Dna-Pkcs Mutation in A Radiosensitive T-B- Scid Patient Inhibits Artemis Activation And Nonhomologous End-Joining
(Amer Soc Clinical Investigation Inc, 2009)Radiosensitive T-B- severe combined immunodeficiency (RS-SCID) is caused by defects in the nonhomologous end-joining (NHEJ) DNA repair pathway, which results in failure of functional V(D)J recombination. Here we have ...