Overview
Congcong Shi practices practicing medicine in Guangzhou, China.
Shi is highly rated in 4 conditions, according to our data. Their clinical expertise encompasses Carnitine-Acylcarnitine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, Methylmalonic Acidemia, and Urea Cycle Disorders (UCD).
They are actively involved in clinical research, co-authoring 20 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 Congcong Shi
Is Congcong Shi a top-rated expert for Carnitine-Acylcarnitine Translocase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Congcong Shi is classified as an Distinguished expert for Carnitine-Acylcarnitine Translocase 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 Congcong Shi participate in research or clinical trials?
Yes. Congcong Shi has published 20 articles and abstracts on conditions like Carnitine-Acylcarnitine Translocase Deficiency. You can view a list of Congcong Shi'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
- Carnitine-Acylcarnitine Translocase Deficiency
- Advanced
- Methylmalonic Acidemia
- Ornithine Transcarbamylase Deficiency
- Urea Cycle Disorders (UCD)
- Experienced
- CitrullinemiaShi isExperienced. Learn about Citrullinemia.
- Delayed GrowthShi isExperienced. Learn about Delayed Growth.
- Inborn Amino Acid Metabolism Disorder
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Nicolaides-Baraitser Syndrome
- PolyhydramniosShi isExperienced. Learn about Polyhydramnios.
- Transient Familial Hyperbilirubinemia