Overview
Zeynep Donbaloglu practices in Antalya, Turkey. Ms. Donbaloglu is highly rated in 5 conditions, according to our data. Her top areas of expertise are Precocious Puberty, Neonatal Severe Hyperparathyroidism, Neonatal Hypothyroidism, Hyperglycerolemia, and Parathyroidectomy.
Her clinical research consists of co-authoring 20 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Congenital HypothyroidismMs. Donbaloglu isAdvanced. Learn about Congenital Hypothyroidism.
- HyperglycerolemiaMs. Donbaloglu isAdvanced. Learn about Hyperglycerolemia.
- Neonatal HypothyroidismMs. Donbaloglu isAdvanced. Learn about Neonatal Hypothyroidism.
- Neonatal Severe HyperparathyroidismMs. Donbaloglu isAdvanced. Learn about Neonatal Severe Hyperparathyroidism.
- Precocious PubertyMs. Donbaloglu isAdvanced. Learn about Precocious Puberty.
- Experienced
- Addison's DiseaseMs. Donbaloglu isExperienced. Learn about Addison's Disease.
- Cardiac TamponadeMs. Donbaloglu isExperienced. Learn about Cardiac Tamponade.
- Congenital Lipoid Adrenal HyperplasiaMs. Donbaloglu isExperienced. Learn about Congenital Lipoid Adrenal Hyperplasia.
- DehydrationMs. Donbaloglu isExperienced. Learn about Dehydration.
- Diabetic KetoacidosisMs. Donbaloglu isExperienced. Learn about Diabetic Ketoacidosis.
- Familial Hyperthyroidism due to Mutations in TSH Receptor