Overview
Heleen Te Brinke practices practicing medicine in Amsterdam, Netherlands.
Ms. Te Brinke is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Hyperlysinemia, Primary Carnitine Deficiency, Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A), and Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome).
She is actively involved in clinical research, co-authoring 16 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 Heleen Te Brinke
Is Heleen Te Brinke a top-rated expert for Hyperlysinemia?
MediFind is an objective health platform that identifies experts based on real-world data. Heleen Te Brinke is classified as an Advanced expert for Hyperlysinemia, 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 Heleen Te Brinke participate in research or clinical trials?
Yes. Heleen Te Brinke has published 16 articles and abstracts on conditions like Hyperlysinemia. You can view a list of Heleen Te Brinke'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
- HyperlysinemiaMs. Te Brinke isAdvanced. Learn about Hyperlysinemia.
- Experienced
- Hereditary Spastic ParaparesisMs. Te Brinke isExperienced. Learn about Hereditary Spastic Paraparesis.
- Mucopolysaccharidoses (MPS)Ms. Te Brinke isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A)
- Primary Carnitine DeficiencyMs. Te Brinke isExperienced. Learn about Primary Carnitine Deficiency.
- Primary Hyperoxaluria Type 1Ms. Te Brinke isExperienced. Learn about Primary Hyperoxaluria Type 1.
- Propionic AcidemiaMs. Te Brinke isExperienced. Learn about Propionic Acidemia.
- Spastic Paraplegia Type 2Ms. Te Brinke isExperienced. Learn about Spastic Paraplegia Type 2.