Overview
Xiaozhou Yuan practices practicing medicine in Beijing, China.
Yuan is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome).
They are actively involved in clinical research, co-authoring 10 peer reviewed articles.
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 Xiaozhou Yuan
Is Xiaozhou Yuan a top-rated expert for Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)?
MediFind is an objective health platform that identifies experts based on real-world data. Xiaozhou Yuan is classified as an Advanced expert for Mucopolysaccharidosis Type 2 (MPS II, Hunter 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 Xiaozhou Yuan participate in research or clinical trials?
Yes. Xiaozhou Yuan has published 10 articles and abstracts on conditions like Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome). You can view a list of Xiaozhou Yuan'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)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Experienced
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)