Overview
Esma Uygur practices practicing medicine in Cerrahpasa, Turkey.
Ms. Uygur is highly rated in 2 conditions, according to our data. Her clinical expertise encompasses 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, Carnitine-Acylcarnitine Translocase Deficiency, Inborn Amino Acid Metabolism Disorder, and Gyrate Atrophy of the Choroid and Retina.
She is actively involved in clinical research, co-authoring 12 peer reviewed articles.
Gender
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.
Frequently Asked Questions about Esma Uygur
Is Esma Uygur a top-rated expert for 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Esma Uygur is classified as an Advanced expert for 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Esma Uygur participate in research or clinical trials?
Yes. Esma Uygur has published 12 articles and abstracts on conditions like 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency. You can view a list of Esma Uygur's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Carnitine-Acylcarnitine Translocase Deficiency
- Experienced
- Cerebrotendinous XanthomatosisMs. Uygur isExperienced. Learn about Cerebrotendinous Xanthomatosis.
- CitrullinemiaMs. Uygur isExperienced. Learn about Citrullinemia.
- Gyrate Atrophy of the Choroid and Retina
- HomocystinuriaMs. Uygur isExperienced. Learn about Homocystinuria.
- Inborn Amino Acid Metabolism DisorderMs. Uygur isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Phenylketonuria (PKU)Ms. Uygur isExperienced. Learn about Phenylketonuria (PKU).
- RhabdomyolysisMs. Uygur isExperienced. Learn about Rhabdomyolysis.
- XanthomaMs. Uygur isExperienced. Learn about Xanthoma.