Ara
Toplam kayıt 569, listelenen: 311-320
Lung transplantation in Turkey: lessons from surgeons and pulmonologists
(TUBITAK SCIENTIFIC & TECHNICAL RESEARCH COUNCIL TURKEY, 2016)
Background/aim: In order to actualize an efficient lung transplantation program, it is necessary to determine priorities and set up strategies. This study aimed to estimate the present situation in Turkey by determining ...
Adipose Tissue Gene Expression of Adiponectin, Tumor Necrosis Factor-alpha and Leptin in Metabolic Syndrome Patients with Coronary Artery Disease
(JAPAN SOC INTERNAL MEDICINE, 2011)
Objective Metabolic syndrome (MS) is associated with an increased risk of coronary artery disease (CAD) and type 2 diabetes mellitus (DM). In MS, adipose tissue has been shown to function as a paracrine and an endocrine ...
Missing atrioventricular echogenic mass during paediatric HeartWare (R) implantation
(VIA MEDICA, 2017)
…
A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP
(NATURE PUBLISHING GROUP, 2016)
The fat mass and obesity associated (FTO) gene has previously been associated with a variety of diseases and conditions, notably obesity, acute coronary syndrome and metabolic syndrome. Reports describing mutations in FTO ...
Use of a magnetic bone nail for lengthening of the femur and tibia
(HONG KONG ACAD MEDICINE PRESS, 2016)
Purpose. To report our experience with the PRECICE nail for limb lengthening in 23 patients. Methods. Records of 15 female and 8 male patients aged 14 to 38 (mean, 23.6) years who underwent lengthening of the tibia (n=6) ...
A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing
(GALENOS YAYINCILIK, 2019)
Objective: Autosomal recessive cutis laxa type IIA (ARCL2A) is a rare congenital disorder characterized by loose arid elastic skin, growth and developmental delay, and skeletal anomalies. It is caused by biallelic mutations ...
Impairment of BRCA1-Related DNA Double-Strand Break Repair Leads to Ovarian Aging in Mice and Humans
(AMER ASSOC ADVANCEMENT SCIENCE, 2013)
The underlying mechanism behind age-induced wastage of the human ovarian follicle reserve is unknown. We identify impaired ATM (ataxia-telangiectasia mutated)-mediated DNA double-strand break (DSB) repair as a cause of ...
Air leak without subcutaneous emphysema in an adult patient due to thyroidectomy
(VIA MEDICA, 2017)
…
Increased Serum G Protein-coupled Estrogen Receptor 1 Levels and Its Diagnostic Value in Drug Naive Patients with Major Depressive Disorder
(KOREAN COLL NEUROPSYCHOPHARMACOLOGY, 2017)
Objective: The facts that depression is more prevalent in females than in males and females are exposed to depression more commonly during certain hormonal fluctuating periods indicate the role of sex hormones in ...
Rapid Desensitization for Immediate Hypersensitivity to Galsulfase Therapy in Patients with MPS VI
(SPRINGER-VERLAG BERLIN, 2016)
Mucopolysaccharidosis type VI (MPS VI) is a progressive, chronic, and multisystem lysosomal storage disease. Enzyme replacement therapy (ERT) with the recombinant human arylsulfatase B enzyme (galsulfase [Naglazyme]) is ...