Overview
Ronald Wanders practices practicing medicine in Amsterdam, Netherlands.
Mr. Wanders is highly rated in 32 conditions, according to our data. His clinical expertise encompasses Zellweger Syndrome, Refsum Disease, Barth Syndrome, and Infantile Refsum Disease.
He is actively involved in clinical research, co-authoring 207 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 Ronald A. Wanders
Is Ronald A. Wanders a top-rated expert for Zellweger Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Ronald A. Wanders is classified as an Elite expert for Zellweger Syndrome, 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 Ronald A. Wanders participate in research or clinical trials?
Yes. Ronald A. Wanders has published 205 articles and abstracts on conditions like Zellweger Syndrome. You can view a list of Ronald A. Wanders'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
- Elite
- Refsum DiseaseMr. Wanders isElite. Learn about Refsum Disease.
- Zellweger SyndromeMr. Wanders isElite. Learn about Zellweger Syndrome.
- Distinguished
- Adrenoleukodystrophy (ALD)Mr. Wanders isDistinguished. Learn about Adrenoleukodystrophy (ALD).
- Barth SyndromeMr. Wanders isDistinguished. Learn about Barth Syndrome.
- Chondrodysplasia Punctata SyndromeMr. Wanders isDistinguished. Learn about Chondrodysplasia Punctata Syndrome.
- Gyrate Atrophy of the Choroid and RetinaMr. Wanders isDistinguished. Learn about Gyrate Atrophy of the Choroid and Retina.
- HyperlysinemiaMr. Wanders isDistinguished. Learn about Hyperlysinemia.
- Infantile Refsum DiseaseMr. Wanders isDistinguished. Learn about Infantile Refsum Disease.
- RhabdomyolysisMr. Wanders isDistinguished. Learn about Rhabdomyolysis.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- X-Linked Chondrodysplasia Punctata 2Mr. Wanders isDistinguished. Learn about X-Linked Chondrodysplasia Punctata 2.
- Advanced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- AchondrogenesisMr. Wanders isAdvanced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMr. Wanders isAdvanced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Addison's DiseaseMr. Wanders isAdvanced. Learn about Addison's Disease.
- CACH SyndromeMr. Wanders isAdvanced. Learn about CACH Syndrome.
- Classic GalactosemiaMr. Wanders isAdvanced. Learn about Classic Galactosemia.
- Glutaric Acidemia Type 2Mr. Wanders isAdvanced. Learn about Glutaric Acidemia Type 2.
- Leigh SyndromeMr. Wanders isAdvanced. Learn about Leigh Syndrome.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Mitochondrial Trifunctional Protein Deficiency
- Newborn Low Blood SugarMr. Wanders isAdvanced. Learn about Newborn Low Blood Sugar.
- Primary Carnitine DeficiencyMr. Wanders isAdvanced. Learn about Primary Carnitine Deficiency.
- Primary Hyperoxaluria Type 1Mr. Wanders isAdvanced. Learn about Primary Hyperoxaluria Type 1.
- Primary Hyperoxaluria Type 3Mr. Wanders isAdvanced. Learn about Primary Hyperoxaluria Type 3.
- Protein DeficiencyMr. Wanders isAdvanced. Learn about Protein Deficiency.
- Pyruvate Carboxylase DeficiencyMr. Wanders isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMr. Wanders isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Sjogren-Larsson SyndromeMr. Wanders isAdvanced. Learn about Sjogren-Larsson Syndrome.
- Experienced
- Arthrogryposis Multiplex CongenitaMr. Wanders isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Batten DiseaseMr. Wanders isExperienced. Learn about Batten Disease.
- Brachydactyly Mononen TypeMr. Wanders isExperienced. Learn about Brachydactyly Mononen Type.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CardiomyopathyMr. Wanders isExperienced. Learn about Cardiomyopathy.
- ChondrodystrophyMr. Wanders isExperienced. Learn about Chondrodystrophy.
- Cohen SyndromeMr. Wanders isExperienced. Learn about Cohen Syndrome.
- Congenital CataractMr. Wanders isExperienced. Learn about Congenital Cataract.
- Congenital ContracturesMr. Wanders isExperienced. Learn about Congenital Contractures.
- Cranioectodermal DysplasiaMr. Wanders isExperienced. Learn about Cranioectodermal Dysplasia.
- Drug Induced DyskinesiaMr. Wanders isExperienced. Learn about Drug Induced Dyskinesia.
- Enlarged LiverMr. Wanders isExperienced. Learn about Enlarged Liver.
- EpilepsyMr. Wanders isExperienced. Learn about Epilepsy.
- Galactokinase DeficiencyMr. Wanders isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Wanders isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Wanders isExperienced. Learn about Galactosemia.
- Hereditary Spastic ParaparesisMr. Wanders isExperienced. Learn about Hereditary Spastic Paraparesis.
- Lactic AcidosisMr. Wanders isExperienced. Learn about Lactic Acidosis.
- Low Blood SugarMr. Wanders isExperienced. Learn about Low Blood Sugar.
- MalnutritionMr. Wanders isExperienced. Learn about Malnutrition.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Metabolic AcidosisMr. Wanders isExperienced. Learn about Metabolic Acidosis.
- Movement DisordersMr. Wanders isExperienced. Learn about Movement Disorders.
- N-Acetylglutamate Synthase DeficiencyMr. Wanders isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- Peroxisomal Acyl-CoA Oxidase DeficiencyMr. Wanders isExperienced. Learn about Peroxisomal Acyl-CoA Oxidase Deficiency.
- Pontocerebellar HypoplasiaMr. Wanders isExperienced. Learn about Pontocerebellar Hypoplasia.
- Primary HyperoxaluriaMr. Wanders isExperienced. Learn about Primary Hyperoxaluria.
- Primary Lateral SclerosisMr. Wanders isExperienced. Learn about Primary Lateral Sclerosis.
- Propionic AcidemiaMr. Wanders isExperienced. Learn about Propionic Acidemia.
- Pyridoxine DeficiencyMr. Wanders isExperienced. Learn about Pyridoxine Deficiency.
- Pyruvate Decarboxylase DeficiencyMr. Wanders isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Riboflavin Transporter Deficiency Neuronopathy
- Schwartz-Jampel SyndromeMr. Wanders isExperienced. Learn about Schwartz-Jampel Syndrome.
- Spastic Paraplegia Type 2Mr. Wanders isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Mr. Wanders isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityMr. Wanders isExperienced. Learn about Spasticity.
- Urea Cycle Disorders (UCD)Mr. Wanders isExperienced. Learn about Urea Cycle Disorders (UCD).
- Usher SyndromeMr. Wanders isExperienced. Learn about Usher Syndrome.
- West SyndromeMr. Wanders isExperienced. Learn about West Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia Tarda