Overview
Naomi Van Vlies practices practicing medicine in Amsterdam, Netherlands.
Ms. Van Vlies is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), and Primary Carnitine Deficiency.
She is actively involved in clinical research, co-authoring 26 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 Naomi N. Van Vlies
Is Naomi N. Van Vlies a top-rated expert for Mucopolysaccharidoses (MPS)?
MediFind is an objective health platform that identifies experts based on real-world data. Naomi N. Van Vlies is classified as an Advanced expert for Mucopolysaccharidoses (MPS), 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 Naomi N. Van Vlies participate in research or clinical trials?
Yes. Naomi N. Van Vlies has published 26 articles and abstracts on conditions like Mucopolysaccharidoses (MPS). You can view a list of Naomi N. Van Vlies'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
- Mucopolysaccharidoses (MPS)Ms. Van Vlies isAdvanced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Experienced
- Brachydactyly Mononen TypeMs. Van Vlies isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyMs. Van Vlies isExperienced. Learn about Chondrodystrophy.
- FucosidosisMs. Van Vlies isExperienced. Learn about Fucosidosis.
- Hereditary Multiple OsteochondromasMs. Van Vlies isExperienced. Learn about Hereditary Multiple Osteochondromas.
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- OsteochondromaMs. Van Vlies isExperienced. Learn about Osteochondroma.
- PertussisMs. Van Vlies isExperienced. Learn about Pertussis.
- Primary Carnitine DeficiencyMs. Van Vlies isExperienced. Learn about Primary Carnitine Deficiency.
- Schwartz-Jampel SyndromeMs. Van Vlies isExperienced. Learn about Schwartz-Jampel Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia TardaMs. Van Vlies isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.