Overview
Huanzheng Li practices practicing medicine in Wenzhou, China.
Li is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Chromosome 6 Uniparental Disomy, Keratosis Follicularis Spinulosa Decalvans, Congenital Contractural Arachnodactyly, and Multiple Pterygium Syndrome.
They are actively involved in clinical research, co-authoring 41 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 Huanzheng Li
Is Huanzheng Li a top-rated expert for Chromosome 6 Uniparental Disomy?
MediFind is an objective health platform that identifies experts based on real-world data. Huanzheng Li is classified as an Advanced expert for Chromosome 6 Uniparental Disomy, 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 Huanzheng Li participate in research or clinical trials?
Yes. Huanzheng Li has published 41 articles and abstracts on conditions like Chromosome 6 Uniparental Disomy. You can view a list of Huanzheng Li'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
- Chromosome 6 Uniparental Disomy
- Keratosis Follicularis Spinulosa Decalvans
- Experienced
- Achard SyndromeLi isExperienced. Learn about Achard Syndrome.
- AlbinismLi isExperienced. Learn about Albinism.
- AnhidrosisLi isExperienced. Learn about Anhidrosis.
- ArachnodactylyLi isExperienced. Learn about Arachnodactyly.
- Arthrogryposis Multiplex Congenita
- Autosomal Recessive Polycystic Kidney Disease
- Becker Muscular Dystrophy
- Congenital Contractural Arachnodactyly
- Congenital ContracturesLi isExperienced. Learn about Congenital Contractures.
- Congenital Insensitivity to Pain with Anhidrosis
- Distal ArthrogryposisLi isExperienced. Learn about Distal Arthrogryposis.
- Distal Arthrogryposis Type 6
- Duchenne Muscular Dystrophy
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Hajdu-Cheney SyndromeLi isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hearing LossLi isExperienced. Learn about Hearing Loss.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- Hermansky-Pudlak Syndrome
- Hypomelanotic DisorderLi isExperienced. Learn about Hypomelanotic Disorder.
- Limb-Girdle Muscular Dystrophy
- MosaicismLi isExperienced. Learn about Mosaicism.
- Multiple Pterygium Syndrome
- Oculocutaneous AlbinismLi isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1
- Oculocutaneous Albinism Type 2
- Perrault SyndromeLi isExperienced. Learn about Perrault Syndrome.
- Spastic Ataxia Charlevoix-Saguenay Type
- Turner SyndromeLi isExperienced. Learn about Turner Syndrome.
- X-Linked Hypophosphatemia