Overview
Jiangxi Xiao practices practicing medicine in Beijing, China.
Xiao is highly rated in 9 conditions, according to our data. Their clinical expertise encompasses Limb-Girdle Muscular Dystrophy Type 2I, Pelizaeus-Merzbacher Disease, X-Linked Retinal Dysplasia, and Fukuyama Type Muscular Dystrophy.
They are actively involved in clinical research, co-authoring 53 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 Jiangxi G. Xiao
Is Jiangxi G. Xiao a top-rated expert for Limb-Girdle Muscular Dystrophy Type 2I?
MediFind is an objective health platform that identifies experts based on real-world data. Jiangxi G. Xiao is classified as an Advanced expert for Limb-Girdle Muscular Dystrophy Type 2I, 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 Jiangxi G. Xiao participate in research or clinical trials?
Yes. Jiangxi G. Xiao has published 53 articles and abstracts on conditions like Limb-Girdle Muscular Dystrophy Type 2I. You can view a list of Jiangxi G. 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
- CACH SyndromeXiao isAdvanced. Learn about CACH Syndrome.
- Fukuyama Type Muscular Dystrophy
- LeukodystrophyXiao isAdvanced. Learn about Leukodystrophy.
- Limb-Girdle Muscular Dystrophy
- Limb-Girdle Muscular Dystrophy Type 2I
- LissencephalyXiao isAdvanced. Learn about Lissencephaly.
- Pelizaeus-Merzbacher Disease
- Walker-Warburg Syndrome
- X-Linked Retinal Dysplasia
- Experienced
- Acute Megakaryoblastic Leukemia
- Acute Myeloid Leukemia (AML)
- Antisynthetase SyndromeXiao isExperienced. Learn about Antisynthetase Syndrome.
- Becker Muscular DystrophyXiao isExperienced. Learn about Becker Muscular Dystrophy.
- Childhood Acute Myeloid Leukemia
- Congenital Fiber-Type Disproportion
- Cortical DysplasiaXiao isExperienced. Learn about Cortical Dysplasia.
- Duchenne Muscular DystrophyXiao isExperienced. Learn about Duchenne Muscular Dystrophy.
- DysarthriaXiao isExperienced. Learn about Dysarthria.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hydrocephalus Skeletal Anomalies
- HypotoniaXiao isExperienced. Learn about Hypotonia.
- LeukemiaXiao isExperienced. Learn about Leukemia.
- Limb-Girdle Muscular Dystrophy Type 1A
- MELAS SyndromeXiao isExperienced. Learn about MELAS Syndrome.
- Menkes DiseaseXiao isExperienced. Learn about Menkes Disease.
- Metachromatic Leukodystrophy
- MyositisXiao isExperienced. Learn about Myositis.
- Necrotizing Myopathy (NM)Xiao isExperienced. Learn about Necrotizing Myopathy (NM).
- Neuronal Intranuclear Inclusion Disease (NIID)
- Tubular Aggregate MyopathyXiao isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular Myopathy