Overview
Lingchao Meng practices practicing medicine in Beijing, China.
Meng is highly rated in 14 conditions, according to our data. Their clinical expertise encompasses Charcot-Marie-Tooth Disease, Becker Muscular Dystrophy, Duchenne Muscular Dystrophy, and Familial Transthyretin Amyloidosis.
They are actively involved in clinical research, co-authoring 99 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 Lingchao H. Meng
Is Lingchao H. Meng a top-rated expert for Charcot-Marie-Tooth Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Lingchao H. Meng is classified as an Advanced expert for Charcot-Marie-Tooth Disease, 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 Lingchao H. Meng participate in research or clinical trials?
Yes. Lingchao H. Meng has published 99 articles and abstracts on conditions like Charcot-Marie-Tooth Disease. You can view a list of Lingchao H. Meng'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
- Becker Muscular Dystrophy
- Charcot-Marie-Tooth Disease
- Chronic Inflammatory Demyelinating Polyneuropathy
- Chronic Polyradiculoneuritis
- Duchenne Muscular Dystrophy
- Familial Transthyretin Amyloidosis
- Necrotizing Myopathy (NM)
- Neuronal Intranuclear Inclusion Disease (NIID)
- Primary AmyloidosisMeng isAdvanced. Learn about Primary Amyloidosis.
- Sensorimotor Polyneuropathy
- Spinal Muscular Atrophy (SMA)
- Spinal Muscular Atrophy Type 2
- Spinal Muscular Atrophy Type 3
- Transthyretin Amyloidosis
- Experienced
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- AnhidrosisMeng isExperienced. Learn about Anhidrosis.
- Antisynthetase SyndromeMeng isExperienced. Learn about Antisynthetase Syndrome.
- Arthrogryposis Multiplex Congenita
- Arthrogryposis Multiplex Congenita Neurogenic Type
- Autonomic NeuropathyMeng isExperienced. Learn about Autonomic Neuropathy.
- CamptocormismMeng isExperienced. Learn about Camptocormism.
- Cardiac AmyloidosisMeng isExperienced. Learn about Cardiac Amyloidosis.
- CardiomyopathyMeng isExperienced. Learn about Cardiomyopathy.
- Cerebral Cavernous Malformation
- Congenital ContracturesMeng isExperienced. Learn about Congenital Contractures.
- Congenital Fiber-Type Disproportion
- Continuous Muscle Fiber Activity Hereditary
- Delta-SarcoglycanopathyMeng isExperienced. Learn about Delta-Sarcoglycanopathy.
- DiarrheaMeng isExperienced. Learn about Diarrhea.
- Drug Induced DyskinesiaMeng isExperienced. Learn about Drug Induced Dyskinesia.
- DysferlinopathyMeng isExperienced. Learn about Dysferlinopathy.
- DystrophinopathyMeng isExperienced. Learn about Dystrophinopathy.
- End-Stage Renal Disease (ESRD)
- Eosinophilic EnteropathyMeng isExperienced. Learn about Eosinophilic Enteropathy.
- Familial Dilated Cardiomyopathy
- Inclusion Body MyositisMeng isExperienced. Learn about Inclusion Body Myositis.
- Infantile Axonal NeuropathyMeng isExperienced. Learn about Infantile Axonal Neuropathy.
- Isaacs' SyndromeMeng isExperienced. Learn about Isaacs' Syndrome.
- Limb-Girdle Muscular Dystrophy
- Membranous NephropathyMeng isExperienced. Learn about Membranous Nephropathy.
- Mitochondrial Complex 1 Deficiency
- Mitochondrial Trifunctional Protein Deficiency
- MyositisMeng isExperienced. Learn about Myositis.
- NecrosisMeng isExperienced. Learn about Necrosis.
- Peripheral NeuropathyMeng isExperienced. Learn about Peripheral Neuropathy.
- Potassium-Aggravated Myotonia
- Primary Lateral SclerosisMeng isExperienced. Learn about Primary Lateral Sclerosis.
- ShinglesMeng isExperienced. Learn about Shingles.
- Spinocerebellar Degeneration and Corneal Dystrophy
- Tubular Aggregate MyopathyMeng isExperienced. Learn about Tubular Aggregate Myopathy.
- VasculitisMeng isExperienced. Learn about Vasculitis.
- X-Linked Dominant Scapuloperoneal Myopathy
- X-Linked Myotubular Myopathy