A5101945921- Sexual Differentiation and Disorders
- Foreign Body Medical Cases
- Pectus Deformity Diagnosis and Treatment
- Restraint-Related Deaths
- Viral gastroenteritis research and epidemiology
- Testicular diseases and treatments
- Diabetes, Cardiovascular Risks, and Lipoproteins
- Virus-based gene therapy research
- Cerebral Palsy and Movement Disorders
- Amoebic Infections and Treatments
- Infectious Diseases and Tuberculosis
- Heart rate and cardiovascular health
- Inflammatory Biomarkers in Disease Prognosis
- Diabetes and associated disorders
- Congenital Anomalies and Fetal Surgery
- Pancreatic function and diabetes
- Urological Disorders and Treatments
- Genetics and Neurodevelopmental Disorders
- Respiratory viral infections research
- Orthopedic Infections and Treatments
- Urologic and reproductive health conditions
Başkent University
2018-2021
Ege University
2017
Sivas State Hospital
2014-2015
The clinical, laboratory, genetic properties and final height of a large cohort patients with nonclassical 21-hydroxylase deficiency (NC21OHD) in Turkey were analyzed.This multicenter, nationwide web-based study collected data.The mean age was 9.79±4.35 years (229 girls, 29 boys). most common symptoms premature pubarche (54.6%) hirsutism (28.6%). peak cortisol found below 18 μg/dL three (15.45%) patients. A mutation detected the CYP21A2 gene 182 (87.5%) V281L. Final female who diagnosed...
In this study, we evaluated the correlation between severity of deformity and cardiopulmonary function with regards to echocardiographic spirometric findings.Twenty-five children, mean age 13.6 years, presenting pectus excavatum August 2012 May 2013, were included. Haller index (HI) was calculated for each patient. Patients an <2.5 accepted as Group 1, 2.5-3.6 2, >3.6 3. Left ventricle dimension, ejection fraction, shortening fraction echocardiography. Using spirometry, forced vital capacity...
What is already known on this topic? study adds?Monogenic diabetes a heterogeneous group of disorders, accounting for just 1-6% all diabetes.Variants in HNF1A, HNF4A, and GCK accounts most MODY-monogenic cases.Patient numbers information are limited less common causes monogenic forms diabetes.This the first Turkish multicenter genetic patients with molecularly diagnosed determined clinical laboratory features, admission characteristics distribution childhood.
Amaç: Akut gastroenteritler çocuklarda morbidite
Background: The purpose of this study was to assess platelet morphological parameters in children and adolescents with type 1 diabetes mellitus (T1DM) determine the factors affecting those parameters. Methods: A total 80 healthy control subjects were included study. All subjects’ including count (PLT), mean volume (MPV), distribution width (PDW) plateletcrit (PCT) levels measured. Age at diagnosis, duration diabetes, hemoglobin A1c (HbA1c) patients T1DM also recorded. Results: There no...
AMA Karabina M, Korkmaz Ö, Aydın S, Atasoy B, Alkan A. Recurrent intradural spinal tuberculosis abscess in a child – follow-up magnetic resonance imaging. Archives of Medical Science - Civilization Diseases. 2016;1(1):75-78. doi:10.5114/amscd.2016.62136. APA Karabina, M., Korkmaz, Ö., Aydın, S., Atasoy, B., & Alkan, (2016). Diseases, 1(1), 75-78. https://doi.org/10.5114/amscd.2016.62136 Chicago Mustafa, Özlem Sinem Bahar and Alpay Alkan. 2016. "Recurrent imaging". Diseases 1 (1): Harvard...