Overview
Qi Ni practices practicing medicine in Shanghai, China.
Mr. Ni is highly rated in 2 conditions, according to our data. His clinical expertise encompasses Hereditary Fructose Intolerance, Fructose-1,6-Bisphosphatase Deficiency, Annular Pancreas, and Chromosome 2 Uniparental Disomy.
He is actively involved in clinical research, co-authoring 49 peer reviewed articles.
Gender
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 Qi Ni
Is Qi Ni a top-rated expert for Hereditary Fructose Intolerance?
MediFind is an objective health platform that identifies experts based on real-world data. Qi Ni is classified as an Advanced expert for Hereditary Fructose Intolerance, 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 Qi Ni participate in research or clinical trials?
Yes. Qi Ni has published 49 articles and abstracts on conditions like Hereditary Fructose Intolerance. You can view a list of Qi Ni'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
- Fructose-1,6-Bisphosphatase Deficiency
- Hereditary Fructose Intolerance
- Experienced
- Annular PancreasMr. Ni isExperienced. Learn about Annular Pancreas.
- Chromosome 2 Uniparental DisomyMr. Ni isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- Congenital Myasthenic SyndromeMr. Ni isExperienced. Learn about Congenital Myasthenic Syndrome.
- DiarrheaMr. Ni isExperienced. Learn about Diarrhea.
- HypotoniaMr. Ni isExperienced. Learn about Hypotonia.
- JaundiceMr. Ni isExperienced. Learn about Jaundice.
- Low Blood SugarMr. Ni isExperienced. Learn about Low Blood Sugar.
- Metabolic AcidosisMr. Ni isExperienced. Learn about Metabolic Acidosis.
- Newborn JaundiceMr. Ni isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarMr. Ni isExperienced. Learn about Newborn Low Blood Sugar.
- OmphaloceleMr. Ni isExperienced. Learn about Omphalocele.
- Patent Ductus ArteriosusMr. Ni isExperienced. Learn about Patent Ductus Arteriosus.
- SeizuresMr. Ni isExperienced. Learn about Seizures.
- Transient Familial Hyperbilirubinemia