Güncel Gönderiler: Araştırma Çıktıları | TR-Dizin | WoS | Scopus | PubMed
Toplam kayıt 3635, listelenen: 3501-3520
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Analysis of the complement pathway mutations in atypical hemolytic uremic syndrome (AHUS)
(Elsevier Ltd., 2014)Background: HUS is characterized by hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the microcirculation of the kidney and other organs. Typical HUS is triggered by infectious agents ... -
Fingolimod in relapsing remitting multiple sclerosis: Short term safety profile
(Sage Publications Ltd., 2014) -
Preimplantation genetic diagnosis (PGD) for single gene disorders/acquired disease with HLA typing: A brief report
(John Wiley and Sons, 2014)Preimplantation Genetic Diagnosis (PGD) of single gene disorders, combined with HLA matching results of “Mikrogen Genetic Laboratory” summarized between the years of 2012–2014. In this report HLA typing was performed for ... -
Replacement of tumor bed after oncoplastic breast-conserving surgery with immediate latissimus dorsi mini-flap
(Elsevier Ltd., 2014)Oncoplastic breast-conserving surgery satisfies oncologic principles of negative margins and improves cosmetic outcomes, even if excision of a considerably large breast volume is required. During this surgical procedure ... -
International consensus project: Neuro-behcet disease
(BMJ Publishing Group, 2014)Aim: Behçet's disease (BD) is a multisystem disease and neurological complications of Behçet's disease [neuro-Behçet's disease (NBD)] are amongst the life threatening and disabling manifestations. Evidence based is limited ... -
Preimplantation genetic diagnosis with carrier mapping test: an encouraging new approach for couples without molecular diagnosis
(Springer Verlag, 2014)Initial step of Preimplantation Genetic Diagnosis for Single Gene Disorders is the investigation of a pathogenic mutation associated with the clinically diagnosed disorder in parents. In some cases clinical diagnosis of ... -
The effect of IL-1B and specific ice/caspase-1 bloker on spike-and-wave discharges
(Wiley-Blackwell, 2011)Purpose: Interleukin (IL)-1b plays a crucial role in the mechanisms of limbic seizures induced in rodent models of temporal lobe epilepsy. We addressed whether activation of the IL-1b signaling occurs in rats with genetic ... -
Electrografic seizures and periodic epileptiform discharges in patients with postanoxic coma
(Wiley-Blackwell, 2012)Purpose: We aimed to examine the predictors and prognostic value of electrographic seizures (ESZs) and periodic epileptiform discharges (PED) of post-anoxic coma patients in intensive care unit (ICU). -
Multiple coronary thrombi with cisplatin
(Health Management Publications, 2014)Testicular cancer is the most common malignancy in young men (15-29 years old). Combination therapy with bleomycin, etoposide, and cisplatin has been the standard first-line treatment for testicular metastatic disease. We ... -
MPL W515L/K mutations in chronic myeloproliferative neoplasms
(Galenos Yayınevi, 2013)The MPL gene encodes the thrombopoietin receptor. Recently MPL mutations (MPL W515L or MPL W515K) were described in patients with essential thrombocythemia (ET) and primary (idiopathic) myelofibrosis (PMF). The prevalence ... -
Effect of epidermal growth factor receptor status on the outcomes of patients with metastatic gastric cancer: A pilot study
(Spandidos Publications, 2014)The expression of epidermal growth factor receptor (EGFR) has been linked to clinical outcome in several solid tumors. However, the clinical significance of EGFR (c-erbB1) in gastric cancer remains unclear. The present ... -
Newborn screening for congenital hypothyroidism
(Galenos Yayınevi, 2013)Introduction Congenital hypothyroidism (CH) is the commonest treatable cause of mental retardation. It is one of the most common disorders related to mental impairment and growth retardation in newborns. In many countries, ... -
The predictive and prognostic significance of c-erb-B2, EGFR, PTEN, mTOR, PI3K, p27, and ERCC1 expression in hepatocellular carcinoma
(Kowsar Corporation, 2012)BACKGROUND: Hepatocellular carcinoma (HCC) is the fifth most common fatal cancer and an important healthcare problem worldwide. There are many studies describing the prognostic and predictive effects of epidermal growth ... -
Minimally invasive plate osteosynthesis (MIPO) in diaphyseal humerus and proximal humerus fractures
(Ekin Medical Publishing, 2012)OBJECTIVE: Our aim was to evaluate the results of minimally invasive plate osteosynthesis (MIPO) using locking plates in diaphyseal humerus andproximal humerus fractures. METHODS: Nine patients who underwent open reduction ... -
Osteotomies/spinal column resections in adult deformity
(Springer Verlag, 2013)Osteotomies may be life saving procedures for patients with rigid severe spinal deformity. Several different types of osteotomies have been defined by several authors. To correct and provide a balanced spine with reasonable ... -
C-reactive protein and lipoprotein-a as markers of coronary heart disease in polycystic ovary syndrome
(Aves Yayıncılık, 2012)OBJECTIVE: The aim of this study was to investigate the risk factors of coronary heart disease, CRP and Lipoprotein-a in polycystic ovary syndrome patients. MATERIAL AND METHODS: Prospectively collected data of polycystic ... -
Comparison of chromosomal abnormality rates in ICSI for non-male factor and spontaneous conception
(Springer Verlag, 2012)OBJECTIVE: To compare cytogenetic data of first-trimester missed abortions in intracytoplasmic sperm injection (ICSI) for non-male factor-mediated and spontaneous pregnancies. METHODS: Using karyotype analysis, we conducted ... -
General evaluation of hepatectomy and hepatocellular carcinoma cases
(Turkish Federation of Pathology Societies, 2011)Objective: Although the clinical and histopathological findings of hepatocellular carcinoma are well described, there are few national studies. In this study, we aimed to investigate the relationship between these findings ... -
First successful preimplantation genetic diagnosis of epidermolysis bullosa with pyloric atresia: Case study of a novel c.4505-4508insACTC mutation
(Springer Verlag, 2012)First successful preimplantation genetic diagnosis of epidermolysis bullosa with pyloric atresia: Case study of a novel c.4505-4508insACTC mutation Introduction Epidermolysis bullosa (EB) is an inherited blistering ... -
Management of a rare case of arrhythmogenic right ventricular dysplasia in pregnancy: a case report
(BioMed Central, 2011)Arrhythmogenic right ventricular dysplasia is a heritable disease of the heart muscle characterized by fibrofatty degeneration of cardiomyocytes. Patients present with ventricular arrhythmias or congestive heart failure, ...
