Overview
Xiuzhen Li practices practicing medicine in Guangzhou, China.
Li is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Multiple Carboxylase Deficiency, GTP Cyclohydrolase 1 Deficiency, Biotinidase Deficiency, and Glycine Encephalopathy.
They are actively involved in clinical research, co-authoring 32 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 Xiuzhen Z. Li
Is Xiuzhen Z. Li a top-rated expert for Multiple Carboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Xiuzhen Z. Li is classified as an Advanced expert for Multiple Carboxylase 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 Xiuzhen Z. Li participate in research or clinical trials?
Yes. Xiuzhen Z. Li has published 32 articles and abstracts on conditions like Multiple Carboxylase Deficiency. You can view a list of Xiuzhen Z. 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
- Multiple Carboxylase Deficiency
- Experienced
- AlkaptonuriaLi isExperienced. Learn about Alkaptonuria.
- Beckwith-Wiedemann Syndrome
- Biotinidase DeficiencyLi isExperienced. Learn about Biotinidase Deficiency.
- Congenital CataractLi isExperienced. Learn about Congenital Cataract.
- Diabetic KetoacidosisLi isExperienced. Learn about Diabetic Ketoacidosis.
- Enlarged LiverLi isExperienced. Learn about Enlarged Liver.
- Epilepsy in ChildrenLi isExperienced. Learn about Epilepsy in Children.
- Familial Multiple Nevi Flammei
- Farber Lipogranulomatosis
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Glycine EncephalopathyLi isExperienced. Learn about Glycine Encephalopathy.
- GTP Cyclohydrolase 1 Deficiency
- Hepatocerebral Degeneration
- HypotoniaLi isExperienced. Learn about Hypotonia.
- Infantile ApneaLi isExperienced. Learn about Infantile Apnea.
- Low Blood SugarLi isExperienced. Learn about Low Blood Sugar.
- Low Sodium LevelLi isExperienced. Learn about Low Sodium Level.
- MacroglossiaLi isExperienced. Learn about Macroglossia.
- Metabolic AcidosisLi isExperienced. Learn about Metabolic Acidosis.
- Methylmalonic AcidemiaLi isExperienced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Newborn Low Blood SugarLi isExperienced. Learn about Newborn Low Blood Sugar.
- OchronosisLi isExperienced. Learn about Ochronosis.
- OmphaloceleLi isExperienced. Learn about Omphalocele.
- Patent Ductus Arteriosus
- Patent Foramen OvaleLi isExperienced. Learn about Patent Foramen Ovale.
- Pompe DiseaseLi isExperienced. Learn about Pompe Disease.
- Prader-Willi SyndromeLi isExperienced. Learn about Prader-Willi Syndrome.
- Precocious PubertyLi isExperienced. Learn about Precocious Puberty.
- Pseudohypoaldosteronism Type 1
- Pseudohypoaldosteronism Type 2
- Stork BiteLi isExperienced. Learn about Stork Bite.
- Type 1 Diabetes (T1D)Li isExperienced. Learn about Type 1 Diabetes (T1D).
- Umbilical HerniaLi isExperienced. Learn about Umbilical Hernia.
- Wilson DiseaseLi isExperienced. Learn about Wilson Disease.
- X-Linked Hypophosphatemia