Overview
Bicheng Yang practices practicing medicine in Nanchang, China.
Yang is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Thalassemia, and Genetic Epilepsy with Febrile Seizures Plus (GEFS+).
They are actively involved in clinical research, co-authoring 46 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 Bicheng Yang
Is Bicheng Yang a top-rated expert for Maternal Hyperphenylalaninemia?
MediFind is an objective health platform that identifies experts based on real-world data. Bicheng Yang is classified as an Distinguished expert for Maternal Hyperphenylalaninemia, 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 Bicheng Yang participate in research or clinical trials?
Yes. Bicheng Yang has published 46 articles and abstracts on conditions like Maternal Hyperphenylalaninemia. You can view a list of Bicheng Yang'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
- Distinguished
- Maternal HyperphenylalaninemiaYang isDistinguished. Learn about Maternal Hyperphenylalaninemia.
- Advanced
- Phenylketonuria (PKU)Yang isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- AdenomyosisYang isExperienced. Learn about Adenomyosis.
- Alpha ThalassemiaYang isExperienced. Learn about Alpha Thalassemia.
- Alport SyndromeYang isExperienced. Learn about Alport Syndrome.
- AnemiaYang isExperienced. Learn about Anemia.
- Beta ThalassemiaYang isExperienced. Learn about Beta Thalassemia.
- Cavernous LymphangiomaYang isExperienced. Learn about Cavernous Lymphangioma.
- Cleft Lip and PalateYang isExperienced. Learn about Cleft Lip and Palate.
- Congenital Hemolytic AnemiaYang isExperienced. Learn about Congenital Hemolytic Anemia.
- Cystic HygromaYang isExperienced. Learn about Cystic Hygroma.
- Early Infantile Epileptic Encephalopathy
- EndometriosisYang isExperienced. Learn about Endometriosis.
- Familial DeafnessYang isExperienced. Learn about Familial Deafness.
- Fetal EdemaYang isExperienced. Learn about Fetal Edema.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Gestational Trophoblastic Disease
- Hearing LossYang isExperienced. Learn about Hearing Loss.
- HemoglobinopathyYang isExperienced. Learn about Hemoglobinopathy.
- Hemolytic AnemiaYang isExperienced. Learn about Hemolytic Anemia.
- Hemolytic Disease of the Newborn
- Hydatidiform MoleYang isExperienced. Learn about Hydatidiform Mole.
- Hydrops FetalisYang isExperienced. Learn about Hydrops Fetalis.
- Hygroma CervicalYang isExperienced. Learn about Hygroma Cervical.
- HypotoniaYang isExperienced. Learn about Hypotonia.
- Infant Hearing LossYang isExperienced. Learn about Infant Hearing Loss.
- Infant Respiratory Distress Syndrome
- Intrauterine Growth Restriction
- Nonsyndromic Hearing LossYang isExperienced. Learn about Nonsyndromic Hearing Loss.
- Propionic AcidemiaYang isExperienced. Learn about Propionic Acidemia.
- ThalassemiaYang isExperienced. Learn about Thalassemia.
- Urea Cycle Disorders (UCD)Yang isExperienced. Learn about Urea Cycle Disorders (UCD).
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency