Overview
Eugenie Dekkers practices practicing medicine in Bilthoven, Netherlands.
Ms. Dekkers is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses Primary Carnitine Deficiency, Tyrosinemia Type 1, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Adrenoleukodystrophy (ALD).
She is actively involved in clinical research, co-authoring 18 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 Eugenie M. Dekkers
Is Eugenie M. Dekkers a top-rated expert for Primary Carnitine Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Eugenie M. Dekkers is classified as an Advanced expert for Primary Carnitine 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 Eugenie M. Dekkers participate in research or clinical trials?
Yes. Eugenie M. Dekkers has published 18 articles and abstracts on conditions like Primary Carnitine Deficiency. You can view a list of Eugenie M. Dekkers'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
- Adrenoleukodystrophy (ALD)Ms. Dekkers isAdvanced. Learn about Adrenoleukodystrophy (ALD).
- Primary Carnitine DeficiencyMs. Dekkers isAdvanced. Learn about Primary Carnitine Deficiency.
- Tyrosinemia Type 1Ms. Dekkers isAdvanced. Learn about Tyrosinemia Type 1.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Addison's DiseaseMs. Dekkers isExperienced. Learn about Addison's Disease.
- Adrenal Insufficiency PediatricMs. Dekkers isExperienced. Learn about Adrenal Insufficiency Pediatric.
- CACH SyndromeMs. Dekkers isExperienced. Learn about CACH Syndrome.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Maternal HyperphenylalaninemiaMs. Dekkers isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Mitochondrial Trifunctional Protein Deficiency
- Newborn Low Blood SugarMs. Dekkers isExperienced. Learn about Newborn Low Blood Sugar.
- Primary Lateral SclerosisMs. Dekkers isExperienced. Learn about Primary Lateral Sclerosis.
- Propionic AcidemiaMs. Dekkers isExperienced. Learn about Propionic Acidemia.
- Protein DeficiencyMs. Dekkers isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisMs. Dekkers isExperienced. Learn about Rhabdomyolysis.
- Severe Combined Immunodeficiency (SCID)Ms. Dekkers isExperienced. Learn about Severe Combined Immunodeficiency (SCID).