Overview
Xiaoning Liu practices practicing medicine in Kunming, China.
Their clinical expertise encompasses Glucose-6-Phosphate Translocase Deficiency, Leukocyte Adhesion Deficiency Type 1, ICF Syndrome, and Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1).
They are actively involved in clinical research, co-authoring 9 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 Xiaoning Liu
Is Xiaoning Liu a top-rated expert for Glucose-6-Phosphate Translocase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Xiaoning Liu is classified as an Experienced expert for Glucose-6-Phosphate Translocase 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 Xiaoning Liu participate in research or clinical trials?
Yes. Xiaoning Liu has published 9 articles and abstracts on conditions like Glucose-6-Phosphate Translocase Deficiency. You can view a list of Xiaoning Liu'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
- Experienced
- Apolipoprotein C2 Deficiency
- Brachydactyly Mononen Type
- ChondrodystrophyLiu isExperienced. Learn about Chondrodystrophy.
- Embryonal Tumor with Multilayered Rosettes
- Familial Hypertriglyceridemia
- Familial Lipoprotein Lipase Deficiency
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Glucose-6-Phosphate Translocase Deficiency
- ICF SyndromeLiu isExperienced. Learn about ICF Syndrome.
- Leukocyte Adhesion Deficiency Type 1
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MononucleosisLiu isExperienced. Learn about Mononucleosis.
- NeuroblastomaLiu isExperienced. Learn about Neuroblastoma.
- Schwartz-Jampel SyndromeLiu isExperienced. Learn about Schwartz-Jampel Syndrome.
- Short Stature (Growth Disorders)
- Wiskott-Aldrich SyndromeLiu isExperienced. Learn about Wiskott-Aldrich Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia Tarda