A5018834773- Renal Diseases and Glomerulopathies
- Vascular anomalies and interventions
- Platelet Disorders and Treatments
- Hematopoietic Stem Cell Transplantation
- Metabolism and Genetic Disorders
- Cell Adhesion Molecules Research
- Ion Transport and Channel Regulation
- Polyomavirus and related diseases
- Infectious Encephalopathies and Encephalitis
- Alcohol Consumption and Health Effects
- Pediatric health and respiratory diseases
- Muscle and Compartmental Disorders
- Bone and Joint Diseases
- Neonatal Health and Biochemistry
- Vascular Procedures and Complications
- IgG4-Related and Inflammatory Diseases
- Epilepsy research and treatment
- Immune Cell Function and Interaction
- Cancer, Hypoxia, and Metabolism
- ATP Synthase and ATPases Research
- Radiomics and Machine Learning in Medical Imaging
- Pharmacological Effects and Toxicity Studies
- Mitochondrial Function and Pathology
- Renal and Vascular Pathologies
- Human Health and Disease
Ankara Atatürk Eğitim ve Araştırma Hastanesi
2024-2025
Trakya University
2025
Hacettepe University
2020-2023
Ankara University
2016-2023
Beykent University
2016
Abstract Childhood obesity is a global health problem with increasing prevalence, leading to long-term cardiovascular complications. Research conducted on adults has established correlation between serum uric acid creatinine ratio (SUA/Cr) and metabolic syndrome (MetS) components. The study investigates the relationship SUA/Cr hypertension (HT) MetS components in children obesity. A total of 103 who underwent ambulatory blood pressure measurement (ABPM) were included patients divided into...
Venlafaxine is a selective serotonin noradrenaline reuptake inhibitor and commonly prescribed antidepressant in adults. Most patients overdosing with venlafaxine develop only mild symptoms. Severe toxicity reported the most common symptoms being CNS depression, toxicity, seizure, or cardiac conduction abnormalities. However, lactic acidosis an uncommon adverse effect. Here, we present first case literature reporting due to overuse adolescent.
A genetic defect of 11 β-hydroxysteroid dehydrogenase causes apparent mineralocorticoid excess syndrome. Since 50 days life, our patient was hospitalized several times for various reasons including hypokalemia. At the age 3.3 years, she diagnosed with severe hypertension (160/120 mmHg). She also had left ventricular hypertrophy and hypertensive retinopathy referred to center. Her renal function electrolytes were normal except on captopril treatment; nifedipine propranolol added. Plasma renin...
Nutcracker phenomenon (NP) is defined as the compression of left renal vein, often occurring between aorta and superior mesenteric artery (SMA). Patients with symptoms associated anatomy are called “Nutcracker syndrome” (NCS). Renal vein results in venous congestion, outlet obstruction, increased pressure vein. The clinical manifestations NCS children vary widely depending on severity compression. It can range from being asymptomatic to presenting intermittent or persistent micro...
Background. Alport syndrome (AS) is characterized by progressive kidney disease. There increasing evidence that renin-angiotensin-aldosterone system (RAAS) inhibition delays chronic disease (CKD) while the effectiveness of immunosuppressive (IS) therapy in AS still uncertain. In this study, we aimed to analyze outcomes pediatric patients with X-linked (XLAS) who received RAAS inhibitors and IS therapy. Methods. Seventy-four children XLAS were included multicenter study. Demographic features,...
Objectives: Febrile seizure (FS) is the most common neurological disorder in childhood.Intermittent rectal diazepam (DZP) prophylaxis seems to prevent recurrence, however, there remains ongoing discussion regarding its ability epilepsy.This study aimed analyze outcome of intermittent prophylactic DZP treatment on both recurrence and subsequent epilepsy. Materials Methods:A total 229 children with FS given between 1 January 2005 December 2013 were included.Data demographics, clinical...
Abstract Background and Aims The aim of the study is to investigate incidence risk factors hypertension (HT) chronic kidney disease (CKD) in patients who had hematopoietic stem cell transplantation (HSCT) during their childhood. Method Patients HSCT between January 2010-2019 with a minimum follow-up period 6 months were included study. Data regarding renal complications collected from medical records patients. Guidelines European Society Hypertension (ESH) American Academy Pediatrics (APA)...
Abstract Background and Aims Alport syndrome (AS) is an inherited glomerular basement membrane disease caused by mutations in COL4A3, COL4A4 or COL4A5 genes. Recently, it has been reported that focal segmental glomerulosclerosis (FSGS) can be seen AS COL4A detected FSGS. In this study, we aimed to define the clinical characteristics of patients with genetically confirmed AS, order establish genotype-phenotype correlation investigate effects different treatment regimes. Method A total 87...
Abstract Background and Aims Urinary system complications after hematopoietic stem cell transplantation (HSCT) cause severe morbidity mortality. The aim of the study is to investigate incidence risk factors urinary in patients who had HSCT during their childhood. Method Patients between January 2010-2019 with a minimum follow-up period 6 months were included study. Data regarding collected from medical records patients. pRIFLE KDIGO classification systems used for definition acute kidney...
Abstract Background and Aims Urinary system complications after hematopoietic stem cell transplantation (HSCT) cause severe morbidity mortality. The aim of the study is to investigate incidence risk factors urinary in patients who had HSCT during their childhood. Method Patients between January 2010-2019 with a minimum follow-up period 6 months were included study. Data regarding collected from medical records patients. pRIFLE KDIGO classification systems used for definition acute kidney...