Overview
Kun Xia practices in Changsha, China. Xia is rated as an Advanced expert by MediFind in the treatment of Adenosine Monophosphate Deaminase Deficiency. Their top areas of expertise are Autism Spectrum Disorder, Spinocerebellar Ataxia Type 3, Olivopontocerebellar Atrophy, Percutaneous Coronary Intervention (PCI), and Angioplasty.
Their clinical research consists of co-authoring 460 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 2 articles in the study of Adenosine Monophosphate Deaminase Deficiency.
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.
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
- Autism Spectrum DisorderXia isDistinguished. Learn about Autism Spectrum Disorder.
- Drug Induced DyskinesiaXia isDistinguished. Learn about Drug Induced Dyskinesia.
- Olivopontocerebellar AtrophyXia isDistinguished. Learn about Olivopontocerebellar Atrophy.
- Oral Squamous Cell CarcinomaXia isDistinguished. Learn about Oral Squamous Cell Carcinoma.
- Spinocerebellar AtaxiaXia isDistinguished. Learn about Spinocerebellar Ataxia.
- Spinocerebellar Ataxia Type 3Xia isDistinguished. Learn about Spinocerebellar Ataxia Type 3.
- Advanced
- Acute Cerebellar Ataxia
- Adenosine Monophosphate Deaminase Deficiency
- Axenfeld-Rieger Syndrome
- Charcot-Marie-Tooth Disease
- Familial Dysautonomia
- Hereditary AtaxiaXia isAdvanced. Learn about Hereditary Ataxia.
- Experienced
- Achalasia Microcephaly Syndrome
- Acute Coronary SyndromeXia isExperienced. Learn about Acute Coronary Syndrome.
- Adenylosuccinate Lyase Deficiency
- Alport SyndromeXia isExperienced. Learn about Alport Syndrome.
- Alzheimer's DiseaseXia isExperienced. Learn about Alzheimer's Disease.
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)