Overview
Yao Zhang practices in Tianjin, China. Mr. Zhang is highly rated in 6 conditions, according to our data. His top areas of expertise are Methylmalonic Acidemia, Succinic Semialdehyde Dehydrogenase Deficiency, Homocystinuria, and Leigh Syndrome.
His clinical research consists of co-authoring 63 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
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
- Distinguished
- Methylmalonic AcidemiaMr. Zhang isDistinguished. Learn about Methylmalonic Acidemia.
- Advanced
- Anti-NMDA Receptor EncephalitisMr. Zhang isAdvanced. Learn about Anti-NMDA Receptor Encephalitis.
- HomocystinuriaMr. Zhang isAdvanced. Learn about Homocystinuria.
- Leigh SyndromeMr. Zhang isAdvanced. Learn about Leigh Syndrome.
- Succinic Semialdehyde Dehydrogenase Deficiency
- Vitamin B12 Deficiency AnemiaMr. Zhang isAdvanced. Learn about Vitamin B12 Deficiency Anemia.
- Experienced
- Absence SeizureMr. Zhang isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly SyndromeMr. Zhang isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Angelman SyndromeMr. Zhang isExperienced. Learn about Angelman Syndrome.
- Argininosuccinic AciduriaMr. Zhang isExperienced. Learn about Argininosuccinic Aciduria.
- CACH SyndromeMr. Zhang isExperienced. Learn about CACH Syndrome.
- Carbamoyl Phosphate Synthetase 1 Deficiency