Overview
Yilun Tao practices practicing medicine in Changzhi, China.
Tao is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Tyrosinemia Type 3, Childhood Hypophosphatasia (HPP), Chromosome 2 Uniparental Disomy, and Pantothenate Kinase-Associated Neurodegeneration.
They are actively involved in clinical research, co-authoring 15 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 Yilun Tao
Is Yilun Tao a top-rated expert for Tyrosinemia Type 3?
MediFind is an objective health platform that identifies experts based on real-world data. Yilun Tao is classified as an Advanced expert for Tyrosinemia Type 3, 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 Yilun Tao participate in research or clinical trials?
Yes. Yilun Tao has published 15 articles and abstracts on conditions like Tyrosinemia Type 3. You can view a list of Yilun Tao'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
- Tyrosinemia Type 3Tao isAdvanced. Learn about Tyrosinemia Type 3.
- Experienced
- Alagille SyndromeTao isExperienced. Learn about Alagille Syndrome.
- Childhood Hypophosphatasia (HPP)
- Chromosome 2 Uniparental Disomy
- Congenital HypothyroidismTao isExperienced. Learn about Congenital Hypothyroidism.
- DysarthriaTao isExperienced. Learn about Dysarthria.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hearing LossTao isExperienced. Learn about Hearing Loss.
- HypoparathyroidismTao isExperienced. Learn about Hypoparathyroidism.
- Hypophosphatasia (HPP)Tao isExperienced. Learn about Hypophosphatasia (HPP).
- HypotoniaTao isExperienced. Learn about Hypotonia.
- Maternal Hyperphenylalaninemia
- Pantothenate Kinase-Associated Neurodegeneration
- Phenylketonuria (PKU)Tao isExperienced. Learn about Phenylketonuria (PKU).
- PurpuraTao isExperienced. Learn about Purpura.
- SeizuresTao isExperienced. Learn about Seizures.
- SpasticityTao isExperienced. Learn about Spasticity.