Overview
Peter Schielen practices practicing medicine in Maarssen, Netherlands.
Mr. Schielen is highly rated in 8 conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Galactose Epimerase Deficiency, and Galactokinase Deficiency.
He is actively involved in clinical research, co-authoring 74 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 Peter I. Schielen
Is Peter I. Schielen a top-rated expert for Classic Galactosemia?
MediFind is an objective health platform that identifies experts based on real-world data. Peter I. Schielen is classified as an Advanced expert for Classic Galactosemia, 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 Peter I. Schielen participate in research or clinical trials?
Yes. Peter I. Schielen has published 74 articles and abstracts on conditions like Classic Galactosemia. You can view a list of Peter I. Schielen'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
- Classic GalactosemiaMr. Schielen isAdvanced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMr. Schielen isAdvanced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMr. Schielen isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMr. Schielen isAdvanced. Learn about Galactosemia.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Phenylketonuria (PKU)Mr. Schielen isAdvanced. Learn about Phenylketonuria (PKU).
- Severe Combined Immunodeficiency (SCID)
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Congenital Adrenal Hyperplasia (CAH)Mr. Schielen isExperienced. Learn about Congenital Adrenal Hyperplasia (CAH).
- Congenital HypothyroidismMr. Schielen isExperienced. Learn about Congenital Hypothyroidism.
- Cystic FibrosisMr. Schielen isExperienced. Learn about Cystic Fibrosis.
- Down SyndromeMr. Schielen isExperienced. Learn about Down Syndrome.
- HypothyroidismMr. Schielen isExperienced. Learn about Hypothyroidism.
- IntersexMr. Schielen isExperienced. Learn about Intersex.
- Maple Syrup Urine DiseaseMr. Schielen isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaMr. Schielen isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Neonatal HypothyroidismMr. Schielen isExperienced. Learn about Neonatal Hypothyroidism.
- PreeclampsiaMr. Schielen isExperienced. Learn about Preeclampsia.
- Primary Lateral SclerosisMr. Schielen isExperienced. Learn about Primary Lateral Sclerosis.