Overview
Shengnan Wu practices practicing medicine in Shanghai, China.
Wu is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Circumferential Skin Creases Kunze Type, Pitt-Hopkins Syndrome, Deafness Hypogonadism Syndrome, and Hypotonia.
They are actively involved in clinical research, co-authoring 28 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 Shengnan Wu
Is Shengnan Wu a top-rated expert for Circumferential Skin Creases Kunze Type?
MediFind is an objective health platform that identifies experts based on real-world data. Shengnan Wu is classified as an Advanced expert for Circumferential Skin Creases Kunze Type, 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 Shengnan Wu participate in research or clinical trials?
Yes. Shengnan Wu has published 28 articles and abstracts on conditions like Circumferential Skin Creases Kunze Type. You can view a list of Shengnan Wu'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
- Circumferential Skin Creases Kunze Type
- Pitt-Hopkins Syndrome
- Experienced
- Achalasia Microcephaly Syndrome
- Adrenoleukodystrophy (ALD)
- Alstrom SyndromeWu isExperienced. Learn about Alstrom Syndrome.
- Atelosteogenesis Type 1Wu isExperienced. Learn about Atelosteogenesis Type 1.
- Autosomal Dominant Hyper IgE Syndrome
- Beta-Propeller Protein-Associated Neurodegeneration
- Brachydactyly Mononen Type
- Congenital Myasthenic Syndrome
- Cortical DysplasiaWu isExperienced. Learn about Cortical Dysplasia.
- Cutis LaxaWu isExperienced. Learn about Cutis Laxa.
- Deafness Hypogonadism Syndrome
- DiarrheaWu isExperienced. Learn about Diarrhea.
- EpilepsyWu isExperienced. Learn about Epilepsy.
- Glycine EncephalopathyWu isExperienced. Learn about Glycine Encephalopathy.
- Hyper IgE SyndromeWu isExperienced. Learn about Hyper IgE Syndrome.
- HyperventilationWu isExperienced. Learn about Hyperventilation.
- HypotoniaWu isExperienced. Learn about Hypotonia.
- IPEX SyndromeWu isExperienced. Learn about IPEX Syndrome.
- Leigh SyndromeWu isExperienced. Learn about Leigh Syndrome.
- MicrocephalyWu isExperienced. Learn about Microcephaly.
- Mitochondrial Complex 1 Deficiency
- Mouth SoresWu isExperienced. Learn about Mouth Sores.
- Mouth UlcersWu isExperienced. Learn about Mouth Ulcers.
- Nijmegen Breakage Syndrome
- Partial Familial Epilepsy
- SeizuresWu isExperienced. Learn about Seizures.
- X-Linked Spondyloepiphyseal Dysplasia Tarda