Overview
Lingfei Luo practices practicing medicine in Shanghai, China.
Luo is highly rated in 1 condition, according to our data. Their clinical expertise encompasses Craniofacial-Deafness-Hand Syndrome, Fountain Syndrome, Camptodactyly Taurinuria, and Camptodactyly Syndrome Guadalajara Type 2.
They are actively involved in clinical research, co-authoring 105 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 Lingfei J. Luo
Is Lingfei J. Luo a top-rated expert for Craniofacial-Deafness-Hand Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Lingfei J. Luo is classified as an Advanced expert for Craniofacial-Deafness-Hand Syndrome, 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 Lingfei J. Luo participate in research or clinical trials?
Yes. Lingfei J. Luo has published 105 articles and abstracts on conditions like Craniofacial-Deafness-Hand Syndrome. You can view a list of Lingfei J. Luo'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
- Craniofacial-Deafness-Hand Syndrome
- Experienced
- Acromicric DysplasiaLuo isExperienced. Learn about Acromicric Dysplasia.
- AgranulocytosisLuo isExperienced. Learn about Agranulocytosis.
- Autosomal Dominant Polycystic Kidney Disease
- Autosomal Recessive Polycystic Kidney Disease
- Bacterial GastroenteritisLuo isExperienced. Learn about Bacterial Gastroenteritis.
- Bacterial MeningitisLuo isExperienced. Learn about Bacterial Meningitis.
- Brachydactyly Mononen Type
- Brain AbscessLuo isExperienced. Learn about Brain Abscess.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly TaurinuriaLuo isExperienced. Learn about Camptodactyly Taurinuria.
- Cartilage-Hair HypoplasiaLuo isExperienced. Learn about Cartilage-Hair Hypoplasia.
- ChondrodystrophyLuo isExperienced. Learn about Chondrodystrophy.
- Congenital Heart Disease (CHD)
- Deafness Craniofacial Syndrome
- EmpyemaLuo isExperienced. Learn about Empyema.
- Enlarged LiverLuo isExperienced. Learn about Enlarged Liver.
- Fountain SyndromeLuo isExperienced. Learn about Fountain Syndrome.
- Hirschsprung DiseaseLuo isExperienced. Learn about Hirschsprung Disease.
- Infantile NeutropeniaLuo isExperienced. Learn about Infantile Neutropenia.
- MeningitisLuo isExperienced. Learn about Meningitis.
- NecrosisLuo isExperienced. Learn about Necrosis.
- PeriodontitisLuo isExperienced. Learn about Periodontitis.
- Polycystic Kidney DiseaseLuo isExperienced. Learn about Polycystic Kidney Disease.
- Schwartz-Jampel SyndromeLuo isExperienced. Learn about Schwartz-Jampel Syndrome.
- Subdural EffusionLuo isExperienced. Learn about Subdural Effusion.
- Werner SyndromeLuo isExperienced. Learn about Werner Syndrome.
- X-Linked Spondyloepiphyseal Dysplasia Tarda