A5078180078- Pediatric Urology and Nephrology Studies
- Urinary Tract Infections Management
- Pelvic floor disorders treatments
- Urinary Bladder and Prostate Research
- Bladder and Urothelial Cancer Treatments
- Ion Transport and Channel Regulation
- Kidney Stones and Urolithiasis Treatments
- Dialysis and Renal Disease Management
- Renal and related cancers
- Electrolyte and hormonal disorders
- Folate and B Vitamins Research
- Intestinal Malrotation and Obstruction Disorders
- Epilepsy research and treatment
- Urological Disorders and Treatments
- Cardiovascular Health and Disease Prevention
- Ion channel regulation and function
- Liver Diseases and Immunity
- Diabetes and associated disorders
- Diet and metabolism studies
- Cardiovascular Disease and Adiposity
- Connective tissue disorders research
- Diabetes Management and Research
- Cardiovascular Function and Risk Factors
- Pediatric Hepatobiliary Diseases and Treatments
- Pharmacological Effects and Toxicity Studies
Gaziantep Children's Hospital
2024
Adıyaman University
2022-2024
Karadeniz Technical University
2018-2019
Vitamin D insufficiency/rickets is a metabolic bone disease that leads to insufficient mineralization of bone. Chronic neurological diseases, including cerebral palsy (CP), convulsive disorders, neural tube defects, myopathy, immobility, lack sun exposure, inadequate nutrition, and antiepileptic drugs (AEDs) can cause vitamin insufficiency osteopenia in children.In this study, the authors searched frequency causative factors children with chronic diseases such as CP, hypoxic-ischemic...
Objective: With this study, we aimed to evaulate the relationship between daytime urinary incontinence and transverse rectal diameter by using transabdominal ultrasound. Method: In pediatric patients were evaluated with symptoms of referred nephrology clinics XXX University Faculty Medicine November 1, 2022 January 2023. This observational, cross-sectional study was carried out after obtaining ethics approval. The Dysfunctional Voiding Symptom Score developed International Children’s...
Objectives: Urinary system infections (UTIs) are among the most common affecting pediatric age group. We aim to show distribution of pathogenic microorganisms and antimicrobial resistance patterns urinary tract select appropriate antibiotherapy in Also, we wanted determine signs symptoms, predisposing factors, imaging findings UTIs. Material Methods: In this study, Elazığ Fethi Sekin City Hospital health registry was screened retrospectively obtain data about results urinalysis, urine...
The aim of this study was to determine whether diabetes mellitus has a high risk diabetic ketoacidosis-related complications. Biochemical parameters affect the resolution time ketoacidosis.
Patients suffering from hypermobility spectrum disorders (HSDs) present with problems related to the musculoskeletal system and have generalized joint without a diagnosed systemic rheumatological disease. HSDs represent an underlying risk factor for many clinical conditions, such as dysfunctional voiding functional constipation (FC). In this study, we investigated ways detect frequency of HSDs, dysfunction (VD), FC in school-aged children assessed their relationship each other....
Objectives Urinary incontinence (UI) is a frequent cause of admission to pediatric nephrology outpatient clinics. The aim this study was determine whether anatomical changes in lower urinary tract structures (retrovesical angulation [RVA] and bladder neck position [BNP]) are associated with UI patients daytime‐wetting comparison healthy children. Methods In prospective study, daytime diagnosed using the Dysfunctional Voiding Symptom Score International Children's Continence Society...
<br>Antenatal Bartter syndrome (BS) is an autosomal recessive hereditary renal tubular disorder caused by mutation in the <i>solute carrier family 12 member 1</i> (<i>SLC12A1</i>) <i>gene</i> on chromosome 15q21.1. This characterized polyuria, hyponatremia, hypokalemic hypochloremic metabolic alkalosis, and hypercalciuria associated with increased urinary loss of electrolytes. Herein, we report a very low-birth-weight premature newborn antenatal BS novel homozygous <i>SLC12A1 gene</i>,...