Overview
Jos Ruiter practices practicing medicine in Amsterdam, Netherlands.
Mr. Ruiter is highly rated in 3 conditions, according to our data. His clinical expertise encompasses Protein Deficiency, Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency, Mitochondrial Trifunctional Protein Deficiency, and N-Acetylglutamate Synthase Deficiency.
He is actively involved in clinical research, co-authoring 24 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 Jos N. Ruiter
Is Jos N. Ruiter a top-rated expert for Protein Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Jos N. Ruiter is classified as an Advanced expert for Protein 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 Jos N. Ruiter participate in research or clinical trials?
Yes. Jos N. Ruiter has published 24 articles and abstracts on conditions like Protein Deficiency. You can view a list of Jos N. Ruiter'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
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Mitochondrial Trifunctional Protein Deficiency
- Protein DeficiencyMr. Ruiter isAdvanced. Learn about Protein Deficiency.
- Experienced
- Arthrogryposis Multiplex CongenitaMr. Ruiter isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Barth SyndromeMr. Ruiter isExperienced. Learn about Barth Syndrome.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- CardiomyopathyMr. Ruiter isExperienced. Learn about Cardiomyopathy.
- Classic GalactosemiaMr. Ruiter isExperienced. Learn about Classic Galactosemia.
- Congenital ContracturesMr. Ruiter isExperienced. Learn about Congenital Contractures.
- Galactokinase DeficiencyMr. Ruiter isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Ruiter isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Ruiter isExperienced. Learn about Galactosemia.
- Glutaric Acidemia Type 2Mr. Ruiter isExperienced. Learn about Glutaric Acidemia Type 2.
- Gyrate Atrophy of the Choroid and Retina
- Hereditary Spastic ParaparesisMr. Ruiter isExperienced. Learn about Hereditary Spastic Paraparesis.
- Leigh SyndromeMr. Ruiter isExperienced. Learn about Leigh Syndrome.
- N-Acetylglutamate Synthase DeficiencyMr. Ruiter isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- Pontocerebellar HypoplasiaMr. Ruiter isExperienced. Learn about Pontocerebellar Hypoplasia.
- Primary Carnitine DeficiencyMr. Ruiter isExperienced. Learn about Primary Carnitine Deficiency.
- Primary Hyperoxaluria Type 1Mr. Ruiter isExperienced. Learn about Primary Hyperoxaluria Type 1.
- RhabdomyolysisMr. Ruiter isExperienced. Learn about Rhabdomyolysis.
- Spastic Paraplegia Type 2Mr. Ruiter isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Mr. Ruiter isExperienced. Learn about Spastic Paraplegia Type 7.
- Urea Cycle Disorders (UCD)Mr. Ruiter isExperienced. Learn about Urea Cycle Disorders (UCD).