Ferda EVİN
Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı
Araştırma alanları: Tıp, Sağlık Bilimleri, Dahili Tıp Bilimleri, Çocuk Sağlığı ve Hastalıkları, Pediatrik Endokrinoloji ve Metabolizma, Endokrinoloji ve Metabolizma Hastalıkları, İç Hastalıkları, Pediatrik Genetik ve Teratoloji
Yayınlar
- 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)
- Basal and Bolus Insulin Distribution According to Treatment Modality: Data from SWEET Diabetes Registry (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)
- 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)
- Neurobehavioral effects of long‐term maternal fructose intake in rat offspring (2018)
- Determining Risk Factors of Epilepsy in Children with Cerebral Palsy: A Retrospective Study (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)
- Solunum yolunda yabancı cisim saptanan 2 infant (2016)
- Sadece perikardit olmayabilir; Üç adölesan erkekte myoperikardit (2016)
- İntrakranial patolojili hastaların faklı prezentasyonları (2016)
- Extübasyon sonrası nadir komplikasyon: Post obstrüktif akciğer ödemi (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)