Overview
Rong Qiang practices practicing medicine in Xi'an, China.
Qiang is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Spondylocostal Dysostosis, and Meier-Gorlin Syndrome.
They are actively involved in clinical research, co-authoring 49 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 Rong Y. Qiang
Is Rong Y. Qiang a top-rated expert for Maternal Hyperphenylalaninemia?
MediFind is an objective health platform that identifies experts based on real-world data. Rong Y. Qiang is classified as an Advanced 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 Rong Y. Qiang participate in research or clinical trials?
Yes. Rong Y. Qiang has published 49 articles and abstracts on conditions like Maternal Hyperphenylalaninemia. You can view a list of Rong Y. Qiang'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
- Maternal Hyperphenylalaninemia
- Phenylketonuria (PKU)Qiang isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Brachydactyly Mononen TypeQiang isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyQiang isExperienced. Learn about Chondrodystrophy.
- Chromosome 13q DuplicationQiang isExperienced. Learn about Chromosome 13q Duplication.
- Congenital Adrenal Hyperplasia (CAH)
- Down SyndromeQiang isExperienced. Learn about Down Syndrome.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Inborn Amino Acid Metabolism Disorder
- IntersexQiang isExperienced. Learn about Intersex.
- Meier-Gorlin SyndromeQiang isExperienced. Learn about Meier-Gorlin Syndrome.
- Methylmalonic AcidemiaQiang isExperienced. Learn about Methylmalonic Acidemia.
- MyelomeningoceleQiang isExperienced. Learn about Myelomeningocele.
- Primary Lateral SclerosisQiang isExperienced. Learn about Primary Lateral Sclerosis.
- Rett SyndromeQiang isExperienced. Learn about Rett Syndrome.
- Schwartz-Jampel SyndromeQiang isExperienced. Learn about Schwartz-Jampel Syndrome.
- Spondylocostal DysostosisQiang isExperienced. Learn about Spondylocostal Dysostosis.
- Trisomy 13Qiang isExperienced. Learn about Trisomy 13.
- X-Linked Spondyloepiphyseal Dysplasia Tarda