Overview
Faquan Lin practices practicing medicine in Nanning, China.
Lin is highly rated in 6 conditions, according to our data. Their clinical expertise encompasses Dysfibrinogenemia, Familial Hypofibrinogenemia, Congenital Afibrinogenemia, and Hereditary Spherocytosis.
They are actively involved in clinical research, co-authoring 79 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 Faquan Q. Lin
Is Faquan Q. Lin a top-rated expert for Dysfibrinogenemia?
MediFind is an objective health platform that identifies experts based on real-world data. Faquan Q. Lin is classified as an Distinguished expert for Dysfibrinogenemia, 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 Faquan Q. Lin participate in research or clinical trials?
Yes. Faquan Q. Lin has published 79 articles and abstracts on conditions like Dysfibrinogenemia. You can view a list of Faquan Q. Lin'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
- Distinguished
- Congenital AfibrinogenemiaLin isDistinguished. Learn about Congenital Afibrinogenemia.
- DysfibrinogenemiaLin isDistinguished. Learn about Dysfibrinogenemia.
- Familial HypofibrinogenemiaLin isDistinguished. Learn about Familial Hypofibrinogenemia.
- Hereditary SpherocytosisLin isDistinguished. Learn about Hereditary Spherocytosis.
- Advanced
- Autoimmune Hemolytic Anemia
- Blood ClotsLin isAdvanced. Learn about Blood Clots.
- Experienced
- Alpha ThalassemiaLin isExperienced. Learn about Alpha Thalassemia.
- AnemiaLin isExperienced. Learn about Anemia.
- Apolipoprotein C2 Deficiency
- Autosomal Recessive Polycystic Kidney Disease
- Congenital Generalized Lipodystrophy
- Congenital Hemolytic Anemia
- Factor 7 DeficiencyLin isExperienced. Learn about Factor 7 Deficiency.
- Familial Lipoprotein Lipase Deficiency
- GigantismLin isExperienced. Learn about Gigantism.
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Hearing LossLin isExperienced. Learn about Hearing Loss.
- HemoglobinopathyLin isExperienced. Learn about Hemoglobinopathy.
- Hemolytic AnemiaLin isExperienced. Learn about Hemolytic Anemia.
- Hereditary ElliptocytosisLin isExperienced. Learn about Hereditary Elliptocytosis.
- Hereditary OvalocytosisLin isExperienced. Learn about Hereditary Ovalocytosis.
- ICF SyndromeLin isExperienced. Learn about ICF Syndrome.
- MalnutritionLin isExperienced. Learn about Malnutrition.
- ThalassemiaLin isExperienced. Learn about Thalassemia.