Overview
Zhenhua Zhao practices practicing medicine in Zhengzhou, China.
Zhao is highly rated in 3 conditions, according to our data. Their clinical expertise encompasses Phenylketonuria (PKU), Dyschromatosis Symmetrica Hereditaria, Maternal Hyperphenylalaninemia, and Duchenne Muscular Dystrophy.
They are actively involved in clinical research, co-authoring 44 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 Zhenhua D. Zhao
Is Zhenhua D. Zhao a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Zhenhua D. Zhao is classified as an Advanced expert for Phenylketonuria (PKU), 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 Zhenhua D. Zhao participate in research or clinical trials?
Yes. Zhenhua D. Zhao has published 44 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Zhenhua D. Zhao'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
- Dyschromatosis Symmetrica Hereditaria
- Maternal Hyperphenylalaninemia
- Phenylketonuria (PKU)Zhao isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- AmenorrheaZhao isExperienced. Learn about Amenorrhea.
- Becker Muscular DystrophyZhao isExperienced. Learn about Becker Muscular Dystrophy.
- Blood ClotsZhao isExperienced. Learn about Blood Clots.
- Cleidocranial DysplasiaZhao isExperienced. Learn about Cleidocranial Dysplasia.
- Congenital Adrenal Hyperplasia (CAH)
- Cortical DysplasiaZhao isExperienced. Learn about Cortical Dysplasia.
- Duchenne Muscular DystrophyZhao isExperienced. Learn about Duchenne Muscular Dystrophy.
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Familial Glucocorticoid Deficiency
- Hemophilia AZhao isExperienced. Learn about Hemophilia A.
- IntersexZhao isExperienced. Learn about Intersex.
- Maple Syrup Urine DiseaseZhao isExperienced. Learn about Maple Syrup Urine Disease.
- Methylmalonic AcidemiaZhao isExperienced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidoses (MPS)Zhao isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Pigmented Purpuric Dermatosis
- Primary Lateral SclerosisZhao isExperienced. Learn about Primary Lateral Sclerosis.
- Spinal Muscular Atrophy (SMA)
- Wilson DiseaseZhao isExperienced. Learn about Wilson Disease.
- X-Linked Severe Combined Immunodeficiency