Overview
Haibo Li practices practicing medicine in Ningbo, China.
Li is highly rated in 14 conditions, according to our data. Their clinical expertise encompasses Cytochrome P450 Oxidoreductase Deficiency, Mosaic Trisomy 9, Miller Syndrome, and Chromosome 6q Duplication.
They are actively involved in clinical research, co-authoring 131 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 Haibo N. Li
Is Haibo N. Li a top-rated expert for Cytochrome P450 Oxidoreductase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Haibo N. Li is classified as an Distinguished expert for Cytochrome P450 Oxidoreductase 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 Haibo N. Li participate in research or clinical trials?
Yes. Haibo N. Li has published 131 articles and abstracts on conditions like Cytochrome P450 Oxidoreductase Deficiency. You can view a list of Haibo N. 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
- Distinguished
- Cytochrome P450 Oxidoreductase Deficiency
- Mosaic Trisomy 9Li isDistinguished. Learn about Mosaic Trisomy 9.
- Advanced
- Bifid NoseLi isAdvanced. Learn about Bifid Nose.
- Blepharocheilodontic Syndrome
- Carnitine-Acylcarnitine Translocase Deficiency
- CHARGE SyndromeLi isAdvanced. Learn about CHARGE Syndrome.
- Chromosome 6q Duplication
- Coffin-Siris Syndrome
- Kabuki SyndromeLi isAdvanced. Learn about Kabuki Syndrome.
- MicrognathiaLi isAdvanced. Learn about Micrognathia.
- Miller SyndromeLi isAdvanced. Learn about Miller Syndrome.
- MosaicismLi isAdvanced. Learn about Mosaicism.
- OmphaloceleLi isAdvanced. Learn about Omphalocele.
- Trisomy 18Li isAdvanced. Learn about Trisomy 18.
- Experienced
- 15q11.2 MicrodeletionLi isExperienced. Learn about 15q11.2 Microdeletion.
- 46XX Testicular Disorder of Sex Development
- Acrofacial Dysostosis Rodriguez Type
- Acrofrontofacionasal Dysostosis Syndrome
- Acromicric DysplasiaLi isExperienced. Learn about Acromicric Dysplasia.
- Arthrogryposis Multiplex Congenita
- Becker Muscular Dystrophy
- Brachydactyly Mononen Type
- Branchio-Oculo-Facial Syndrome (BOFS)
- Branchiootorenal Syndrome
- Cafe-Au-Lait SpotsLi isExperienced. Learn about Cafe-Au-Lait Spots.
- ChondrodystrophyLi isExperienced. Learn about Chondrodystrophy.
- ChoroideremiaLi isExperienced. Learn about Choroideremia.
- Color BlindnessLi isExperienced. Learn about Color Blindness.
- Congenital ContracturesLi isExperienced. Learn about Congenital Contractures.
- Congenital Hemolytic Anemia
- Corpus Callosum Agenesis
- Cortical DysplasiaLi isExperienced. Learn about Cortical Dysplasia.
- CraniosynostosisLi isExperienced. Learn about Craniosynostosis.
- Crouzon SyndromeLi isExperienced. Learn about Crouzon Syndrome.
- Cutis LaxaLi isExperienced. Learn about Cutis Laxa.
- Duchenne Muscular Dystrophy
- DystrophinopathyLi isExperienced. Learn about Dystrophinopathy.
- EctropionLi isExperienced. Learn about Ectropion.
- EpilepsyLi isExperienced. Learn about Epilepsy.
- Fetal Akinesia SequenceLi isExperienced. Learn about Fetal Akinesia Sequence.
- Fountain SyndromeLi isExperienced. Learn about Fountain Syndrome.
- Fructose-1,6-Bisphosphatase Deficiency
- Glucose-6-Phosphate Dehydrogenase Deficiency
- Hearing LossLi isExperienced. Learn about Hearing Loss.
- Hemolytic AnemiaLi isExperienced. Learn about Hemolytic Anemia.
- HypotoniaLi isExperienced. Learn about Hypotonia.
- Infant Hearing LossLi isExperienced. Learn about Infant Hearing Loss.
- IntersexLi isExperienced. Learn about Intersex.
- Metabolic AcidosisLi isExperienced. Learn about Metabolic Acidosis.
- MicrophthalmiaLi isExperienced. Learn about Microphthalmia.
- MigraineLi isExperienced. Learn about Migraine.
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Muenke SyndromeLi isExperienced. Learn about Muenke Syndrome.
- Newborn Low Blood SugarLi isExperienced. Learn about Newborn Low Blood Sugar.
- OsteoarthritisLi isExperienced. Learn about Osteoarthritis.
- Osteomyelitis in Children
- Otitis Media with Effusion
- Patent Foramen OvaleLi isExperienced. Learn about Patent Foramen Ovale.
- PolydactylyLi isExperienced. Learn about Polydactyly.
- PolyhydramniosLi isExperienced. Learn about Polyhydramnios.
- Pontocerebellar Hypoplasia
- Progressive External Ophthalmoplegia
- Protein C DeficiencyLi isExperienced. Learn about Protein C Deficiency.
- Rhizomelic SyndromeLi isExperienced. Learn about Rhizomelic Syndrome.
- Schwartz-Jampel Syndrome
- Severe Combined Immunodeficiency (SCID)
- Short Rib-Polydactyly Syndrome Type 1
- Smith-Lemli-Opitz Syndrome
- Spondyloenchondrodysplasia
- SyndactylyLi isExperienced. Learn about Syndactyly.
- Testicular TorsionLi isExperienced. Learn about Testicular Torsion.
- Treacher Collins Syndrome
- Ventricular Septal Defects
- Vici SyndromeLi isExperienced. Learn about Vici Syndrome.
- Waardenburg SyndromeLi isExperienced. Learn about Waardenburg Syndrome.
- Waardenburg Syndrome Type 1
- X-Linked Spondyloepiphyseal Dysplasia Tarda