Ferda EVİN

Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı Ve Hastalıkları Anabilim Dalı

Research areas: Medicine, Health Sciences, Internal Medicine Sciences, Child Health and Diseases, Pediatric Endocrinology and Metabolism, Endocrinology and Metabolic Diseases, Internal Diseases, Pediatric Genetics and Teratology

Publications

Detection of copy number variations by chromosomal microarray analysis in disorders of sex development of unexplained molecular etiology and association with clinical findings (2025)
“Predicting diabetic kidney disease in youth with type 1 diabetes: Insights from genetic risk assessment” (2024)
Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation (2024)
Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta (2024)
ABCC8-related maturity-onset diabetes of the young: Switching from insulin to sulphonylurea therapy: How long do we need for a good metabolic control? (2023)
Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene (2023)
A case-control study of early-stage radiological markers of endothelial dysfunction and cardiovascular findings in patients with osteogenesis imperfecta: genotype–phenotype correlations (2023)
Molecular diagnosis in patients with monogenic diabetes mellitus, and detection of a novel candidate gene (2023)
Basal and Bolus Insulin Distribution According to Treatment Modality: Data from SWEET Diabetes Registry (2023)
46,XY Cinsiyet Gelişim Bozukluğu - Testis Farklılaşma Bozuklukları (2023)
Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition (2022)
Prediction of Transient or Permanent Congenital Hypothyroidism (2022)
Endokrin Bozucular ve Üreme Sistemi (2021)
Molecular Genetic Diagnosis and Research of Candidate Genes by Targeted Next Generation Sequence Analysis and Whole Exome Sequencing Method in Monogenic Diabetes: MODY-TURK Project (2021)
Predictive low-glucose suspend system and glycemic variability (2021)
Molecular Genetic Diagnosis and Research of Candidate Genes by Targeted Next Generation Sequence Analysis and Whole Exome Sequencing Method in Monogenic Diabetes: MODY-TURK Project (2021)
Glycated Hemoglobin Variability and Microvascular Complications in Patients with Type 1 Diabetes Mellitus (2021)
The Value of Telemedicine for the Follow-up of Patients with New Onset Type 1 Diabetes Mellitus During COVID-19 Pandemic in Turkey: A Report of Eight Cases (2020)
Treatment and long-term follow-up of patients diagnosed with type 1 diabetes mellitus before age 5 (2020)
Glycated hemoglobin variability and microvascular complications in patients with type 1 diabetes mellitus (2020)
Continuous subcutaneous insulin infusion in preschool children with type 1 diabetes mellitus as initial treatment: Effect on glycemic control (2020)
Determining Risk Factors of Epilepsy in Children with Cerebral Palsy: A Retrospective Study (2018)
Neurobehavioral effects of long‐term maternal fructose intake in rat offspring (2018)
Evaluation of long‐term effects of artificial sweeteners on rat brain: a biochemical, behavioral, and histological study (2018)
Risk factors for epilepsy in cases with cerebral palsy: Aretrospective study (2017)
Serebral Felçli Çocuklarda Epilepsi Gelişimi için risk faktörlerinin retrospektif olarak belirlenmesi (2017)
İntrakranial patolojili hastaların faklı prezentasyonları (2016)
Extübasyon sonrası nadir komplikasyon: Post obstrüktif akciğer ödemi (2016)
Solunum yolunda yabancı cisim saptanan 2 infant (2016)
Sadece perikardit olmayabilir; Üç adölesan erkekte myoperikardit (2016)
Nadir görülen bir mikroorganizma: Raoultella ornithinolytica (2016)
It may not only acute pericarditis myopericarditis in 3 adolescent boy (2015)
Juvenile Dermatomyositis with a Rare and Severe Complication: Macrophage Activation Syndrome (2014)