Overview
Qin Zhang practices practicing medicine in Xuhui, China.
Zhang is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Short-Chain Acyl-CoA Dehydrogenase Deficiency, Cockayne Syndrome Type 1, Cockayne Syndrome Type 2, and Congenital Insensitivity to Pain with Anhidrosis.
They are actively involved in clinical research, co-authoring 33 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 Qin H. Zhang
Is Qin H. Zhang 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. Qin H. Zhang is classified as an Distinguished 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 Qin H. Zhang participate in research or clinical trials?
Yes. Qin H. Zhang has published 33 articles and abstracts on conditions like Short-Chain Acyl-CoA Dehydrogenase Deficiency. You can view a list of Qin H. Zhang'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
- Distinguished
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Experienced
- AnhidrosisZhang isExperienced. Learn about Anhidrosis.
- Cleidocranial DysplasiaZhang isExperienced. Learn about Cleidocranial Dysplasia.
- Cockayne SyndromeZhang isExperienced. Learn about Cockayne Syndrome.
- Cockayne Syndrome Type 1Zhang isExperienced. Learn about Cockayne Syndrome Type 1.
- Cockayne Syndrome Type 2Zhang isExperienced. Learn about Cockayne Syndrome Type 2.
- Congenital Insensitivity to Pain with Anhidrosis
- GigantismZhang isExperienced. Learn about Gigantism.
- Hajdu-Cheney SyndromeZhang isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- HypermethioninemiaZhang isExperienced. Learn about Hypermethioninemia.
- Inborn Amino Acid Metabolism Disorder
- InfertilityZhang isExperienced. Learn about Infertility.
- Joubert SyndromeZhang isExperienced. Learn about Joubert Syndrome.
- Methylmalonic AcidemiaZhang isExperienced. Learn about Methylmalonic Acidemia.
- MicrophthalmiaZhang isExperienced. Learn about Microphthalmia.
- Simpson-Golabi-Behmel Syndrome
- Smith-Lemli-Opitz SyndromeZhang isExperienced. Learn about Smith-Lemli-Opitz Syndrome.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency