Overview
Yuanyuan Xiao practices practicing medicine in Deyang, China.
Xiao is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Polyhydramnios, Dyschromatosis Universalis Hereditaria, Cerebellar Hypoplasia, and Hermansky-Pudlak Syndrome.
They are actively involved in clinical research, co-authoring 65 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 Yuanyuan U. Xiao
Is Yuanyuan U. Xiao a top-rated expert for Polyhydramnios?
MediFind is an objective health platform that identifies experts based on real-world data. Yuanyuan U. Xiao is classified as an Advanced expert for Polyhydramnios, 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 Yuanyuan U. Xiao participate in research or clinical trials?
Yes. Yuanyuan U. Xiao has published 65 articles and abstracts on conditions like Polyhydramnios. You can view a list of Yuanyuan U. Xiao'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
- PolyhydramniosXiao isAdvanced. Learn about Polyhydramnios.
- Experienced
- Achalasia Microcephaly Syndrome
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- AlbinismXiao isExperienced. Learn about Albinism.
- Alport SyndromeXiao isExperienced. Learn about Alport Syndrome.
- Alstrom SyndromeXiao isExperienced. Learn about Alstrom Syndrome.
- Cerebellar HypoplasiaXiao isExperienced. Learn about Cerebellar Hypoplasia.
- Chromosome 13q DuplicationXiao isExperienced. Learn about Chromosome 13q Duplication.
- Cortical DysplasiaXiao isExperienced. Learn about Cortical Dysplasia.
- Crouzon SyndromeXiao isExperienced. Learn about Crouzon Syndrome.
- Dyschromatosis Universalis Hereditaria
- Hearing LossXiao isExperienced. Learn about Hearing Loss.
- Heart TumorXiao isExperienced. Learn about Heart Tumor.
- Hermansky-Pudlak SyndromeXiao isExperienced. Learn about Hermansky-Pudlak Syndrome.
- Hypomelanotic DisorderXiao isExperienced. Learn about Hypomelanotic Disorder.
- HypotoniaXiao isExperienced. Learn about Hypotonia.
- Increased Head Circumference
- MELAS SyndromeXiao isExperienced. Learn about MELAS Syndrome.
- MicrocephalyXiao isExperienced. Learn about Microcephaly.
- Oculocutaneous AlbinismXiao isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1
- Oculocutaneous Albinism Type 2
- Pigmented Purpuric Dermatosis
- Pulmonary EdemaXiao isExperienced. Learn about Pulmonary Edema.
- Retinitis PigmentosaXiao isExperienced. Learn about Retinitis Pigmentosa.
- Retinopathy Pigmentary Mental Retardation
- Transient Tic DisorderXiao isExperienced. Learn about Transient Tic Disorder.
- Treacher Collins SyndromeXiao isExperienced. Learn about Treacher Collins Syndrome.
- Trisomy 13Xiao isExperienced. Learn about Trisomy 13.
- Trisomy 18Xiao isExperienced. Learn about Trisomy 18.
- Usher SyndromeXiao isExperienced. Learn about Usher Syndrome.
- Usher Syndrome Type 2AXiao isExperienced. Learn about Usher Syndrome Type 2A.
- X-Linked Retinitis Pigmentosa (XLRP)