Tür "conferenceObject" TR-Dizin İndeksli Yayınlar Koleksiyonu için listeleme
Toplam kayıt 24, listelenen: 1-20
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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 ... -
The antioxidant effect of boric acid in chronic alcohol abuse
(Federation of European Biochemical Societies, 2015)Alcohol is a toxin that causes serious damage on many organs depending on the dose and duration of use. Chronic alcohol consumption is the most important factor that leads to cirrhosis and liver failure. In this study, ... -
ASSOCIATION STUDY OF THE DIO2 GENE AS A SUSCEPTIBILITY CANDIDATE FOR SCHIZOPHRENIA IN THE TURKISH POPULATION; A CASE-CONTROL STUDY
(ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER, 2013)… -
Boric acid supplementation can prevent oxidative damage caused by prenatal alcohol exposure in rat cerebral cortex
(Federation of European Biochemical Societies, 2014)Depending on its acute or chronic usage and the dosage, alcohol has toxic effects on both mother and fetus when it is administered during pregnancy 1. Up till now, fetal alcohol spectrum disorders (FASD) has been shown to ... -
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 ... -
Effects of amantadine on postural instability in Parkinson's disease
(Wiley-Blackwell, 2014)Amantadine is a NMDA antagonist that has antiparkinson properties. Although it is widely used for treatment of 1-dopa related dyskinesias some case reports also mention its effect on postural instability in Parkison’s Disease. -
Effects of kindling stimulations on parvalbumin immunoreactivity in substantia nigra pars reticulata of gaers and wistar rats
(Wiley Online Library, 2014)Purpose: One of the mechanisms that control epileptic seizures involves the neural network in the substantia nigra pars reticulata (SNR). Two functionally discrete regions, SNRanterior and posterior were demonstrated to ... -
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). -
Fingolimod in relapsing remitting multiple sclerosis: Short term safety profile
(Sage Publications Ltd., 2014) -
Genotypic and phenotypic presentation of TTR-FAP in Turkey
(Wiley-Blackwell, 2014)Transthyretin-related familial amyloid polyneuropathy (TTR-FAP) is an autosomal dominant disorder caused by mutations of the transthyretin (TTR) gene. More than 100 different mutations of the transthyretin gene were ... -
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 ... -
Is asking same question in different ways has any impact on student achievement?
(Elsevier, 2014)Objective: In our education system Multiple-choice exams have begun more widespread with each passing day. Multiple choice exams are useful for assessment of students’ lower levels of knowledge while the essays are used ... -
Long-term follow-up of genetic generalized epilepsy with typical absence seizures and generalized paroxysmal fast activity in adulthood
(Wiley, 2014)Introduction: Generalized paroxysmal fast activity (GPFA), a rhythmic EEG pattern of unknown significance was reported in a few patients with genetic generalized epilepsy (GGE) presenting with typical absence seizures ... -
Melatonin's effect on inflammatory cytokines in oxidative stress induced PC12 cells
(Wiley Online Library, 2013)Introduction: Melatonin is primarily synthesized and secreted by the pineal gland. Melatonin participate in many physiological and biochemical functions. The etiology of neurodegenerative diseases has not been well understood. -
MMP2 gene polymorphisms and MMP2 mRNA levels in patients with superficial varices of lower extremities
(The International Institute of Anticancer Research, 2011)Background: Although superficial varices of the lower extremities are common and with high morbidity, their etiology has not been elucidated yet. Previously, it was thought that venous hypertension was responsible for such ... -
mRNA expression levels of elastin, fibulin-5, LOXL-1, MMP-2 and MMP-9 in patients with varicose vein
(Wiley Online Library, 2012)Aim: The reason of varicose vein formation is not exactly known yet; but some morphological and physiological changes of venous wall are thought to be responsible. One of those suspected reasons is the changes in quantity ... -
Perirhinal cortical kindling in genetic absence epilepsy rat strains
(Wiley Online Library, 2010)Purpose: The genetic models of absence epilepsy, GAERS and WAG/ Rij rat strains, are resistant to progression of partial seizures induced by amygdaloid and hippocampal kindling. Perirhinal cortex is a crucial area for the ... -
Plasma acylated ghrelin, obestatin and leptin in different stages of chronic kidney disease patients
(Wiley-Blackwell, 2009)Objective: Malnutrition and loss of appetite remain a frequent problem in patients with chronic kidney disease (CKD). These patients have inflammation accompanied by high levels of plasma leptin, an appetite-modulating ... -
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 ... -
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 ...