Overview
Jianqiang Tan practices practicing medicine in Liuzhou, China.
Tan is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Short-Chain Acyl-CoA Dehydrogenase Deficiency, Isovaleric Acidemia, Primary Carnitine Deficiency, and Carnitine Palmitoyltransferase 1 Deficiency.
They are actively involved in clinical research, co-authoring 17 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 Jianqiang Tan
Is Jianqiang Tan a top-rated expert for Short-Chain Acyl-CoA Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Jianqiang Tan is classified as an Advanced expert for Short-Chain Acyl-CoA Dehydrogenase 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 Jianqiang Tan participate in research or clinical trials?
Yes. Jianqiang Tan has published 17 articles and abstracts on conditions like Short-Chain Acyl-CoA Dehydrogenase Deficiency. You can view a list of Jianqiang Tan'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
- Isovaleric AcidemiaTan isAdvanced. Learn about Isovaleric Acidemia.
- Primary Carnitine Deficiency
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Experienced
- AlbinismTan isExperienced. Learn about Albinism.
- Carnitine Palmitoyltransferase 1 Deficiency
- CitrullinemiaTan isExperienced. Learn about Citrullinemia.
- Congenital Adrenal Hyperplasia (CAH)
- Glutaric Acidemia Type 1Tan isExperienced. Learn about Glutaric Acidemia Type 1.
- Glutaric Acidemia Type 2Tan isExperienced. Learn about Glutaric Acidemia Type 2.
- Hallervorden-Spatz Disease
- Hermansky-Pudlak SyndromeTan isExperienced. Learn about Hermansky-Pudlak Syndrome.
- Hypomelanotic DisorderTan isExperienced. Learn about Hypomelanotic Disorder.
- Inborn Amino Acid Metabolism Disorder
- IntersexTan isExperienced. Learn about Intersex.
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Magnesium DeficiencyTan isExperienced. Learn about Magnesium Deficiency.
- Metabolic AcidosisTan isExperienced. Learn about Metabolic Acidosis.
- Mitochondrial Trifunctional Protein Deficiency
- Noonan SyndromeTan isExperienced. Learn about Noonan Syndrome.
- Oculocutaneous AlbinismTan isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1
- Oculocutaneous Albinism Type 2
- Phenylketonuria (PKU)Tan isExperienced. Learn about Phenylketonuria (PKU).
- Primary Lateral SclerosisTan isExperienced. Learn about Primary Lateral Sclerosis.
- Protein DeficiencyTan isExperienced. Learn about Protein Deficiency.
- RASopathiesTan isExperienced. Learn about RASopathies.
- RhabdomyolysisTan isExperienced. Learn about Rhabdomyolysis.
- Spinal Muscular Atrophy (SMA)
- Spinocerebellar Ataxia Type 3
- Striatonigral Degeneration Infantile
- Urea Cycle Disorders (UCD)