Overview
Hans Waterham practices practicing medicine in Amsterdam, Netherlands.
Mr. Waterham is highly rated in 20 conditions, according to our data. His clinical expertise encompasses Zellweger Syndrome, Refsum Disease, X-Linked Chondrodysplasia Punctata 2, and Chondrodysplasia Punctata Syndrome.
He is actively involved in clinical research, co-authoring 157 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 Hans R. Waterham
Is Hans R. Waterham a top-rated expert for Zellweger Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Hans R. Waterham 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 Hans R. Waterham participate in research or clinical trials?
Yes. Hans R. Waterham has published 157 articles and abstracts on conditions like Zellweger Syndrome. You can view a list of Hans R. Waterham'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
- Zellweger SyndromeMr. Waterham isElite. Learn about Zellweger Syndrome.
- Distinguished
- AchondrogenesisMr. Waterham isDistinguished. Learn about Achondrogenesis.
- Acromesomelic DysplasiaMr. Waterham isDistinguished. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson TypeMr. Waterham isDistinguished. Learn about Acromesomelic Dysplasia Hunter Thompson Type.
- Acromesomelic Dysplasia Maroteaux TypeMr. Waterham isDistinguished. Learn about Acromesomelic Dysplasia Maroteaux Type.
- Chondrodysplasia Punctata SyndromeMr. Waterham isDistinguished. Learn about Chondrodysplasia Punctata Syndrome.
- Mevalonate Kinase DeficiencyMr. Waterham isDistinguished. Learn about Mevalonate Kinase Deficiency.
- Refsum DiseaseMr. Waterham isDistinguished. Learn about Refsum Disease.
- Riboflavin Transporter Deficiency NeuronopathyMr. Waterham isDistinguished. Learn about Riboflavin Transporter Deficiency Neuronopathy.
- X-Linked Chondrodysplasia Punctata 2Mr. Waterham isDistinguished. Learn about X-Linked Chondrodysplasia Punctata 2.
- Advanced
- Addison's DiseaseMr. Waterham isAdvanced. Learn about Addison's Disease.
- Adrenoleukodystrophy (ALD)Mr. Waterham isAdvanced. Learn about Adrenoleukodystrophy (ALD).
- Glutaric Acidemia Type 2Mr. Waterham isAdvanced. Learn about Glutaric Acidemia Type 2.
- Gyrate Atrophy of the Choroid and Retina
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Primary Carnitine DeficiencyMr. Waterham isAdvanced. Learn about Primary Carnitine Deficiency.
- Rhizomelic SyndromeMr. Waterham isAdvanced. Learn about Rhizomelic Syndrome.
- Smith-Lemli-Opitz SyndromeMr. Waterham isAdvanced. Learn about Smith-Lemli-Opitz Syndrome.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- CACH SyndromeMr. Waterham isExperienced. Learn about CACH Syndrome.
- Congenital CataractMr. Waterham isExperienced. Learn about Congenital Cataract.
- Drug Induced DyskinesiaMr. Waterham isExperienced. Learn about Drug Induced Dyskinesia.
- Hearing LossMr. Waterham isExperienced. Learn about Hearing Loss.
- Hereditary Spastic ParaparesisMr. Waterham isExperienced. Learn about Hereditary Spastic Paraparesis.
- Leigh SyndromeMr. Waterham isExperienced. Learn about Leigh Syndrome.
- MalnutritionMr. Waterham isExperienced. Learn about Malnutrition.
- Metabolic AcidosisMr. Waterham isExperienced. Learn about Metabolic Acidosis.
- MosaicismMr. Waterham isExperienced. Learn about Mosaicism.
- Peroxisomal Acyl-CoA Oxidase DeficiencyMr. Waterham isExperienced. Learn about Peroxisomal Acyl-CoA Oxidase Deficiency.
- Perrault SyndromeMr. Waterham isExperienced. Learn about Perrault Syndrome.
- Primary Lateral SclerosisMr. Waterham isExperienced. Learn about Primary Lateral Sclerosis.
- Protein DeficiencyMr. Waterham isExperienced. Learn about Protein Deficiency.
- Spastic Paraplegia Type 2Mr. Waterham isExperienced. Learn about Spastic Paraplegia Type 2.
- Succinic Semialdehyde Dehydrogenase Deficiency
- Trophoblastic Tumor Placental SiteMr. Waterham isExperienced. Learn about Trophoblastic Tumor Placental Site.
- Turner SyndromeMr. Waterham isExperienced. Learn about Turner Syndrome.