Overview
Xiyuan Li practices practicing medicine in Tianjin, China.
Li is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Methylmalonic Acidemia, Succinic Semialdehyde Dehydrogenase Deficiency, and Leigh Syndrome.
They are actively involved in clinical research, co-authoring 26 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 Xiyuan Li
Is Xiyuan Li a top-rated expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Xiyuan Li is classified as an Advanced expert for Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, 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 Xiyuan Li participate in research or clinical trials?
Yes. Xiyuan Li has published 26 articles and abstracts on conditions like Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. You can view a list of Xiyuan Li'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
- Methylmalonic Acidemia
- Succinic Semialdehyde Dehydrogenase Deficiency
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- Absence SeizureLi isExperienced. Learn about Absence Seizure.
- Acromicric DysplasiaLi isExperienced. Learn about Acromicric Dysplasia.
- Angelman SyndromeLi isExperienced. Learn about Angelman Syndrome.
- Argininosuccinic Aciduria
- CitrullinemiaLi isExperienced. Learn about Citrullinemia.
- Geleophysic DysplasiaLi isExperienced. Learn about Geleophysic Dysplasia.
- Generalized Tonic-Clonic Seizure
- Glutaric Acidemia Type 1
- HomocystinuriaLi isExperienced. Learn about Homocystinuria.
- Leigh SyndromeLi isExperienced. Learn about Leigh Syndrome.
- Low Blood SugarLi isExperienced. Learn about Low Blood Sugar.
- MalnutritionLi isExperienced. Learn about Malnutrition.
- Newborn Low Blood SugarLi isExperienced. Learn about Newborn Low Blood Sugar.
- Niemann-Pick DiseaseLi isExperienced. Learn about Niemann-Pick Disease.
- Primary HyperoxaluriaLi isExperienced. Learn about Primary Hyperoxaluria.
- Primary Hyperoxaluria Type 1
- Urea Cycle Disorders (UCD)
- Vitamin B12 Deficiency Anemia