Overview
Mubeccel Demirkol practices practicing medicine in Istanbul, Turkey.
Demirkol is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Beta-Ketothiolase Deficiency, Phenylketonuria (PKU), 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, and Primary Carnitine Deficiency.
They are actively involved in clinical research, co-authoring 20 peer reviewed articles.
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 Mubeccel Demirkol
Is Mubeccel Demirkol a top-rated expert for Beta-Ketothiolase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Mubeccel Demirkol is classified as an Advanced expert for Beta-Ketothiolase 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 Mubeccel Demirkol participate in research or clinical trials?
Yes. Mubeccel Demirkol has published 20 articles and abstracts on conditions like Beta-Ketothiolase Deficiency. You can view a list of Mubeccel Demirkol'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
- Beta-Ketothiolase DeficiencyDemirkol isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Classic GalactosemiaDemirkol isExperienced. Learn about Classic Galactosemia.
- DysarthriaDemirkol isExperienced. Learn about Dysarthria.
- Folate DeficiencyDemirkol isExperienced. Learn about Folate Deficiency.
- Galactokinase DeficiencyDemirkol isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyDemirkol isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDemirkol isExperienced. Learn about Galactosemia.
- Limb-Girdle Muscular DystrophyDemirkol isExperienced. Learn about Limb-Girdle Muscular Dystrophy.
- Maternal HyperphenylalaninemiaDemirkol isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Phenylketonuria (PKU)Demirkol isExperienced. Learn about Phenylketonuria (PKU).
- Primary Carnitine DeficiencyDemirkol isExperienced. Learn about Primary Carnitine Deficiency.
- RhabdomyolysisDemirkol isExperienced. Learn about Rhabdomyolysis.
- Vitamin B12 Deficiency AnemiaDemirkol isExperienced. Learn about Vitamin B12 Deficiency Anemia.