A5066301048- Management and Performance Evaluation
- Folate and B Vitamins Research
- Diabetes and associated disorders
- Metabolism and Genetic Disorders
- Lipid metabolism and disorders
- Diet and metabolism studies
- Occupational Health and Safety Management
- Growth Hormone and Insulin-like Growth Factors
- Belt and Road Initiative
- Pancreatic function and diabetes
- Diet, Metabolism, and Disease
- Metabolomics and Mass Spectrometry Studies
Cukurova University
2019-2024
<title>Abstract</title> <bold>Background/Objective:</bold> This study aims to determine the effects of dietary treatment on growth and biochemical markers in children with primary familial hypercholesterolemia. <bold>Subjects/Methods:</bold> The was conducted 30 aged 5-10 years diagnosed hypercholesterolemia at Cukurova University Hospital. Sociodemographic characteristics habits patients were queried, anthropometric measurements taken. Specific treatments arranged, detailed education...
<h3>Introduction</h3> Phenylketonuria (PKU) is the most common and autosomal recessively inherited metabolic disease due to deficiency of phenylalanine hydroxylase (PAH). Elevated levels are not only toxic for children but also teratogenic fetus. Clinical findings maternal phenylketonuria (MPKU) intrauterine growth retardation, microcephaly, significant developmental delay, congenital cardiac anomalies, some other structural defects. Poorly diet control high blood causes this severe...
Herediter tirozinemi tip-1 (HT1), fumarilasetoasetat hidrolaz enzim eksikliğine bağlı, nadir görülen hepatorenal bir kalıtsal metabolik hastalıktır. yönetiminde, tirozin ve fenilalaninden kısıtlı diyetle birlikte nitisinon tedavisi kullanılması önerilmektedir. Otoimmün diyabet olarak da bilinen Tip-1 Diabetes Mellitus (T1DM), pankreas β-hücre disfonksiyonuna bağlı mutlak insülin eksikliği ile karakterize hiperglisemiye yol açan kronik endokrinolojik Hastalarda glisemik kontrolü sağlamak için...