Overview
Xinwen Huang practices in Hangzhou, China. Huang is rated as an Elite expert by MediFind in the treatment of Primary Carnitine Deficiency. Their top areas of expertise are Primary Carnitine Deficiency, Citrullinemia, Urea Cycle Disorders (UCD), and Isovaleric Acidemia.
Their clinical research consists of co-authoring 79 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 3 articles in the study of Primary Carnitine Deficiency.
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.
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
- Elite
- Primary Carnitine Deficiency
- Distinguished
- CitrullinemiaHuang isDistinguished. Learn about Citrullinemia.
- Urea Cycle Disorders (UCD)Huang isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- Beta-Ketothiolase Deficiency
- Carnitine-Acylcarnitine Translocase Deficiency
- Glutaric Acidemia Type 2
- HyperprolinemiaHuang isAdvanced. Learn about Hyperprolinemia.
- Isovaleric AcidemiaHuang isAdvanced. Learn about Isovaleric Acidemia.
- Metabolic AcidosisHuang isAdvanced. Learn about Metabolic Acidosis.
- Experienced
- AcheiropodyHuang isExperienced. Learn about Acheiropody.
- AlkaptonuriaHuang isExperienced. Learn about Alkaptonuria.
- Arginase DeficiencyHuang isExperienced. Learn about Arginase Deficiency.
- Bile Duct ObstructionHuang isExperienced. Learn about Bile Duct Obstruction.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Carnitine Palmitoyltransferase 1 Deficiency