Başlık için PubMed İndeksli Yayınlar Koleksiyonu listeleme
Toplam kayıt 4087, listelenen: 1907-1926
-
Gallbladder perforation during elective laparoscopic cholecystectomy: Incidence, risk factors, and outcomes
(Kare Publishing, 2018)OBJECTIVE: This study aimed to reveal the risk factors and outcomes of gallbladder perforation (GP) during laparoscopic cholecystectomy. METHODS: Videotapes of all patients who underwent an elective cholecystectomy at our ... -
Gallbladder polyps: Correlation of size and clinicopathologic characteristics based on updated definitions
(Public Library of Science, 2020)Background Different perspectives exist regarding the clinicopathologic characteristics, biology and management of gallbladder polyps. Size is often used as the surrogate evidence of polyp behavior and size of >= 1cm is ... -
Ganglion cysts in the lateral portal region of the knee after arthroscopy: Report of two cases
(Clinical Case Report, 2015)A ganglion cyst (GC) is a mucinous or gelatinous-filled benign tumor overlying a joint or tendon sheath, which commonly arises in the dorsal and volar wrist side but may occur anywhere in the body. Although cystic lesions ... -
GAS6 intron 8 c.834+7G > A gene polymorphism in diabetic nephropathy
(Taylor and Francis, 2015)Background - Aim: In animal experiments, growth arrest-specific 6 (Gas6) protein plays a key role in the development of mesangial cell and glomerular hypertrophy in the early phase of diabetic nephropathy, and diabetic ... -
Gastric cancer prevention from the point of helicobacter
(AVES, 2014)When the first cancer estimates of world were made in 1975, gastric cancer (GC) was the most common neoplasm, making 70% of the total. Although its rate decreased to 6.8% in 2012, it is still the fifth most common malignancy ... -
Gastrointestinal sistem malignitelerinde retansiyon sütürü kullanılan hastaların erken ve geç dönem komplikasyonlarının retrospektif analizi
(AVES, 2015)Amaç: Abdominal tümör cerrahisi sonrası görülen yara iyileşmesi ile ilgili komplikasyonlar hala önemli bir problem olmaya devam etmektedir. Bu komplikasyonların önlenmesinde retansiyon sutürünün önemini belirlemek amacı ... -
GATA3 expression and its relationship with clinicopathological parameters in invasive breast carcinomas
(Elsevier Gmbh, 2017)GATA3, as a transcription factor, is associated with estrogen receptor (ER) expression and necessary for luminal cell differentiation in mammary glands. Association of GATA3 expression with clinicopathological parameters, ... -
Gebelikte tiroid hastalıklarının neonatal etkileri ve TSH yüksekliği olan bebeğe yaklaşım: Türk Neonatoloji ve Çocuk Endokrinoloji ve Diyabet Dernekleri uzlaşı raporu
(AVES, 2018)Fetus ve yenidoğanda tiroid fonksiyonları bebek sağlığı ve merkezisinir sisteminin gelişimi açısından önem taşımaktadır. Annede iyoteksikliği, iyoda maruziyet, tiroid hastalıkları (Hashimoto tiroiditi,Graves’ hastalığı), ... -
Gender inequality in genitourinary malignancies clinical trials leadership
(Springer Science and Business Media Deutschland GmbH, 2024)Background Over the past 2 decades, there has been a growing interest in the signifcance of gender roles in healthcare and several eforts and initiatives have focused on increasing female representation in the medical ... -
Gender-related differences in disease activity and clinical features in patients with peripheral psoriatic arthritis: A multi-center study
(Elsevier Masson s.r.l., 2021)Objective: This study sought to compare disease activity, clinical features, and patient-reported outcomes concerning anxiety, depression, fatigue, function, quality of life, and fibromyalgia between female and male patients ... -
Gene polymorphisms and febrile neutropenia in acute leukemia-no association with IL-4, CCR-5, IL-1RA, but the MBL-2, ACE, and TLR-4 are associated with the disease in Turkish patients: A preliminary study
(Mary Ann Liebert, Inc., 2014)Aims: The aim of this study was to investigate the mannose-binding lectin 2 (MBL-2), interleukin (IL)-4, Toll-like receptor 4 (TLR-4), angiotensin converting enzyme (ACE), chemokine receptor 5 (CCR-5), and IL-1 receptor ... -
Gene-environment interaction in molar-incisor hypomineralization
(Public Library of Science, 2021)Molar incisor hypomineralization (MIH) is an enamel condition characterized by lesions ranging in color from white to brown which present rapid caries progression, and mainly affects permanent first molars and incisors. ... -
General characteristics of paint thinner burns: Single center experience
(Turkish Assoc Trauma Emergency Surgery, 2017)BACKGROUND: The aim of the present study was to present characteristic features and risk factors of paint thinner burns in order to raise awareness and help prevent these injuries. METHODS: Records of patients admitted to ... -
Generalized epileptic seizure in an adolescent idiopathic scoliosis (AIS) patient with syringomyelia after deformity correction surgery
(2013)INTRODUCTION Adolescent idiopathic scoliosis and epilepsy are pathologies rarely seen together. In this study we report an AIS case we operated in which epilepsy was seen post operatively. We want to emphasize the items ... -
Generating a detailed protein profile of Fasciola hepatica during the chronic stage of infection in cattle
(Wiley-Blackwell, 2014)Fasciola hepatica is a trematode helminth causing a damaging disease, fasciolosis, in ruminants and humans. Comprehensive proteomic studies broaden our knowledge of the parasite's protein profile, and provide new insights ... -
Genetic influences on dental enamel that impact caries differ between the primary and permanent dentitions
(Wiley, 2015)Clinically, primary and permanent teeth are distinct anatomically and the presentation of caries lesions differs between the two dentitions. Hence, the possibility exists that genetic contributions to tooth formation of ... -
Genetic mapping of high caries experience on human chromosome 13
(BMC, 2013)Background: Our previous genome-wide linkage scan mapped five loci for caries experience. The purpose of this study was to fine map one of these loci, the locus 13q31.1, in order to identify genetic contributors to caries. ... -
A genetic mimic of cerebral palsy: Homozygous NFU1 mutation with marked intrafamilial phenotypic variation
(Elsevier, 2020)Background: Genetic defects in the NFU1, an iron-sulfur cluster scaffold protein coding gene, which is vital in the final stage of assembly for iron sulfur proteins, have been defined as multiple mitochondrial dysfunctions ... -
Genetic polymorphism in the serotonin transporter gene-linked polymorphic region and response to serotonin reuptake inhibitors in patients with premature ejaculation
(Hospital das Clínicas da Universidade de São Paulo, 2014)OBJECTIVES: Serotonin plays a central role in ejaculation and selective serotonin reuptake inhibitors have been successfully used to treat premature ejaculation. Here, we evaluated the relationship between a polymorphism ... -
Genetic polymorphisms influence shear bond resistance of orthodontic brackets
(Elsevier, 2020)Objectives: The purpose of this study was to determine if shear bond resistance of orthodontic brackets bonded to enamel is associated with genes implicated in the enamel mineralization process.Methods: Ninety-two permanent, ...
