Overview
Hui-chen Ho practices practicing medicine in Datong, Taiwan.
Their clinical expertise encompasses Lymphofollicular Hyperplasia, Biotinidase Deficiency, Multiple Carboxylase Deficiency, and Pompe Disease.
They are actively involved in clinical research, co-authoring 13 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 Hui-chen Ho
Is Hui-chen Ho a top-rated expert for Lymphofollicular Hyperplasia?
MediFind is an objective health platform that identifies experts based on real-world data. Hui-chen Ho is classified as an Experienced expert for Lymphofollicular Hyperplasia, 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 Hui-chen Ho participate in research or clinical trials?
Yes. Hui-chen Ho has published 13 articles and abstracts on conditions like Lymphofollicular Hyperplasia. You can view a list of Hui-chen Ho'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
- Experienced
- Biotinidase DeficiencyHo isExperienced. Learn about Biotinidase Deficiency.
- Congenital Heart Disease (CHD)
- Fabry DiseaseHo isExperienced. Learn about Fabry Disease.
- Gaucher DiseaseHo isExperienced. Learn about Gaucher Disease.
- LaryngomalaciaHo isExperienced. Learn about Laryngomalacia.
- Lymphofollicular Hyperplasia
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Multiple Carboxylase Deficiency
- Pompe DiseaseHo isExperienced. Learn about Pompe Disease.
- ThrombocytopeniaHo isExperienced. Learn about Thrombocytopenia.