Overview
Hidde Huidekoper practices practicing medicine in Rotterdam, Netherlands.
Huidekoper is highly rated in 8 conditions, according to our data. Their clinical expertise encompasses Xanthoma, Cerebrotendinous Xanthomatosis, Classic Galactosemia, and Galactose Epimerase Deficiency.
They are actively involved in clinical research, co-authoring 41 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 Hidde H. Huidekoper
Is Hidde H. Huidekoper a top-rated expert for Xanthoma?
MediFind is an objective health platform that identifies experts based on real-world data. Hidde H. Huidekoper is classified as an Distinguished expert for Xanthoma, 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 Hidde H. Huidekoper participate in research or clinical trials?
Yes. Hidde H. Huidekoper has published 41 articles and abstracts on conditions like Xanthoma. You can view a list of Hidde H. Huidekoper'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
- Distinguished
- Cerebrotendinous XanthomatosisHuidekoper isDistinguished. Learn about Cerebrotendinous Xanthomatosis.
- XanthomaHuidekoper isDistinguished. Learn about Xanthoma.
- Advanced
- Classic GalactosemiaHuidekoper isAdvanced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyHuidekoper isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyHuidekoper isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaHuidekoper isAdvanced. Learn about Galactosemia.
- Glutaric Acidemia Type 2Huidekoper isAdvanced. Learn about Glutaric Acidemia Type 2.
- Pompe DiseaseHuidekoper isAdvanced. Learn about Pompe Disease.
- Experienced
- Andersen DiseaseHuidekoper isExperienced. Learn about Andersen Disease.
- Batten DiseaseHuidekoper isExperienced. Learn about Batten Disease.
- CardiomyopathyHuidekoper isExperienced. Learn about Cardiomyopathy.
- CLN1 DiseaseHuidekoper isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseHuidekoper isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseHuidekoper isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseHuidekoper isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseHuidekoper isExperienced. Learn about CLN5 Disease.
- Erythropoietic ProtoporphyriaHuidekoper isExperienced. Learn about Erythropoietic Protoporphyria.
- HypotoniaHuidekoper isExperienced. Learn about Hypotonia.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- MalnutritionHuidekoper isExperienced. Learn about Malnutrition.
- Mitochondrial Trifunctional Protein Deficiency
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- PorphyriaHuidekoper isExperienced. Learn about Porphyria.
- Primary Carnitine DeficiencyHuidekoper isExperienced. Learn about Primary Carnitine Deficiency.
- Propionic AcidemiaHuidekoper isExperienced. Learn about Propionic Acidemia.
- Protein DeficiencyHuidekoper isExperienced. Learn about Protein Deficiency.
- ProtoporphyriaHuidekoper isExperienced. Learn about Protoporphyria.
- RhabdomyolysisHuidekoper isExperienced. Learn about Rhabdomyolysis.
- Urea Cycle Disorders (UCD)Huidekoper isExperienced. Learn about Urea Cycle Disorders (UCD).