Overview
Jianbo Shu practices practicing medicine in Tianjin, China.
Shu is highly rated in 1 condition, according to our data. Their clinical expertise encompasses FG Syndrome, Succinic Semialdehyde Dehydrogenase Deficiency, Dyschromatosis Symmetrica Hereditaria, and Methylmalonic Acidemia.
They are actively involved in clinical research, co-authoring 23 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 Jianbo Shu
Is Jianbo Shu a top-rated expert for FG Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Jianbo Shu is classified as an Advanced expert for FG Syndrome, 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 Jianbo Shu participate in research or clinical trials?
Yes. Jianbo Shu has published 23 articles and abstracts on conditions like FG Syndrome. You can view a list of Jianbo Shu'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
- FG SyndromeShu isAdvanced. Learn about FG Syndrome.
- Experienced
- Aicardi-Goutieres Syndrome
- Ataxia-TelangiectasiaShu isExperienced. Learn about Ataxia-Telangiectasia.
- Cutis LaxaShu isExperienced. Learn about Cutis Laxa.
- Dyschromatosis Symmetrica Hereditaria
- Enlarged LiverShu isExperienced. Learn about Enlarged Liver.
- EpilepsyShu isExperienced. Learn about Epilepsy.
- Folate DeficiencyShu isExperienced. Learn about Folate Deficiency.
- Glycogen Storage Disease Type 3
- MalnutritionShu isExperienced. Learn about Malnutrition.
- Metabolic AcidosisShu isExperienced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaShu isExperienced. Learn about Methylmalonic Acidemia.
- Neonatal SepsisShu isExperienced. Learn about Neonatal Sepsis.
- Pigmented Purpuric Dermatosis
- Primary Lateral SclerosisShu isExperienced. Learn about Primary Lateral Sclerosis.
- Spinal Muscular Atrophy (SMA)
- Succinic Semialdehyde Dehydrogenase Deficiency
- Transient Familial Hyperbilirubinemia