Overview
Xiaowei Xu practices practicing medicine in Tianjin, China.
Xu is highly rated in 5 conditions, according to our data. Their clinical expertise encompasses Homocystinuria, Limb-Girdle Muscular Dystrophy Type 2A, FG Syndrome, and Familial Short Stature (FSS).
They are actively involved in clinical research, co-authoring 19 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 Xiaowei Xu
Is Xiaowei Xu a top-rated expert for Homocystinuria?
MediFind is an objective health platform that identifies experts based on real-world data. Xiaowei Xu is classified as an Advanced expert for Homocystinuria, 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 Xiaowei Xu participate in research or clinical trials?
Yes. Xiaowei Xu has published 19 articles and abstracts on conditions like Homocystinuria. You can view a list of Xiaowei Xu'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
- Familial Short Stature (FSS)
- FG SyndromeXu isAdvanced. Learn about FG Syndrome.
- HomocystinuriaXu isAdvanced. Learn about Homocystinuria.
- Limb-Girdle Muscular Dystrophy Type 2A
- Metabolic Acidosis
- Experienced
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- HypotoniaXu isExperienced. Learn about Hypotonia.
- IntersexXu isExperienced. Learn about Intersex.
- Limb-Girdle Muscular Dystrophy
- MalnutritionXu isExperienced. Learn about Malnutrition.
- Methylmalonic AcidemiaXu isExperienced. Learn about Methylmalonic Acidemia.
- Methylmalonic Acidemia with Homocystinuria
- Prader-Willi SyndromeXu isExperienced. Learn about Prader-Willi Syndrome.
- Severe Combined Immunodeficiency (SCID)
- Short Stature (Growth Disorders)
- Succinic Semialdehyde Dehydrogenase Deficiency
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Vitamin B12 Deficiency Anemia