Overview
Chuanzhu Yan practices practicing medicine in Qingdao, China.
Yan is highly rated in 24 conditions, according to our data. Their clinical expertise encompasses Glutaric Acidemia Type 2, MELAS Syndrome, Limb-Girdle Muscular Dystrophy, Limb-Girdle Muscular Dystrophy Type 1B, and Thymectomy.
They are actively involved in clinical research, co-authoring 199 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 Chuanzhu L. Yan
Is Chuanzhu L. Yan a top-rated expert for Glutaric Acidemia Type 2?
MediFind is an objective health platform that identifies experts based on real-world data. Chuanzhu L. Yan is classified as an Distinguished expert for Glutaric Acidemia Type 2, 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 Chuanzhu L. Yan participate in research or clinical trials?
Yes. Chuanzhu L. Yan has published 199 articles and abstracts on conditions like Glutaric Acidemia Type 2. You can view a list of Chuanzhu L. Yan'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
- Glutaric Acidemia Type 2Yan isDistinguished. Learn about Glutaric Acidemia Type 2.
- Limb-Girdle Muscular Dystrophy
- Limb-Girdle Muscular Dystrophy Type 1B
- MELAS SyndromeYan isDistinguished. Learn about MELAS Syndrome.
- Advanced
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Cerebrotendinous Xanthomatosis
- Chronic Inflammatory Demyelinating Polyneuropathy
- Congenital Fiber-Type Disproportion
- Cytochrome C Oxidase Deficiency
- DermatomyositisYan isAdvanced. Learn about Dermatomyositis.
- Drug Induced Dyskinesia
- Lactic AcidosisYan isAdvanced. Learn about Lactic Acidosis.
- Leber Hereditary Optic Neuropathy (LHON)
- Myoclonic Epilepsy Associated With Ragged Red Fibers
- MyositisYan isAdvanced. Learn about Myositis.
- Nemaline MyopathyYan isAdvanced. Learn about Nemaline Myopathy.
- Optic Nerve AtrophyYan isAdvanced. Learn about Optic Nerve Atrophy.
- ParaplegiaYan isAdvanced. Learn about Paraplegia.
- PolymyositisYan isAdvanced. Learn about Polymyositis.
- Primary Lateral Sclerosis
- Progressive External Ophthalmoplegia
- Tubular Aggregate Myopathy
- X-Linked Myotubular Myopathy
- XanthomaYan isAdvanced. Learn about Xanthoma.
- Experienced
- Acute Cerebellar AtaxiaYan isExperienced. Learn about Acute Cerebellar Ataxia.
- Adrenoleukodystrophy (ALD)
- Alternating Hemiplegia of Childhood
- Antisynthetase SyndromeYan isExperienced. Learn about Antisynthetase Syndrome.
- Becker Muscular DystrophyYan isExperienced. Learn about Becker Muscular Dystrophy.
- Brown SyndromeYan isExperienced. Learn about Brown Syndrome.
- CACH SyndromeYan isExperienced. Learn about CACH Syndrome.
- CataractYan isExperienced. Learn about Cataract.
- Centronuclear MyopathyYan isExperienced. Learn about Centronuclear Myopathy.
- Cerebral HypoxiaYan isExperienced. Learn about Cerebral Hypoxia.
- Cervical SpondylosisYan isExperienced. Learn about Cervical Spondylosis.
- Charcot-Marie-Tooth Disease
- Chronic Polyradiculoneuritis
- Continuous Muscle Fiber Activity Hereditary
- Cramp-Fasciculation Syndrome
- Cytoplasmic Body MyopathyYan isExperienced. Learn about Cytoplasmic Body Myopathy.
- Dentatorubral-Pallidoluysian Atrophy
- DiarrheaYan isExperienced. Learn about Diarrhea.
- Duchenne Muscular Dystrophy
- DysferlinopathyYan isExperienced. Learn about Dysferlinopathy.
- EclampsiaYan isExperienced. Learn about Eclampsia.
- EncephaloceleYan isExperienced. Learn about Encephalocele.
- Eosinophilic FasciitisYan isExperienced. Learn about Eosinophilic Fasciitis.
- EpilepsyYan isExperienced. Learn about Epilepsy.
- Epilepsy with Myoclonic-Atonic Seizures
- Fatal Familial InsomniaYan isExperienced. Learn about Fatal Familial Insomnia.
- GangliosidosisYan isExperienced. Learn about Gangliosidosis.
- Guillain-Barre SyndromeYan isExperienced. Learn about Guillain-Barre Syndrome.
- Hearing LossYan isExperienced. Learn about Hearing Loss.
- HemiplegiaYan isExperienced. Learn about Hemiplegia.
- HemorrhoidsYan isExperienced. Learn about Hemorrhoids.
- High ArchYan isExperienced. Learn about High Arch.
- HypotoniaYan isExperienced. Learn about Hypotonia.
- Inclusion Body Myopathy 2Yan isExperienced. Learn about Inclusion Body Myopathy 2.
- InsomniaYan isExperienced. Learn about Insomnia.
- Isaacs' SyndromeYan isExperienced. Learn about Isaacs' Syndrome.
- Krabbe DiseaseYan isExperienced. Learn about Krabbe Disease.
- Lafora DiseaseYan isExperienced. Learn about Lafora Disease.
- Lambert-Eaton SyndromeYan isExperienced. Learn about Lambert-Eaton Syndrome.
- Leigh SyndromeYan isExperienced. Learn about Leigh Syndrome.
- LeukodystrophyYan isExperienced. Learn about Leukodystrophy.
- Limb-Girdle Muscular Dystrophy Type 1A
- Limb-Girdle Muscular Dystrophy Type 2I
- MalnutritionYan isExperienced. Learn about Malnutrition.
- Mcleod Neuroacanthocytosis Syndrome
- Monoclonal Gammopathy of Undetermined Significance (MGUS)
- MosaicismYan isExperienced. Learn about Mosaicism.
- Movement DisordersYan isExperienced. Learn about Movement Disorders.
- Muscle AtrophyYan isExperienced. Learn about Muscle Atrophy.
- Myasthenia GravisYan isExperienced. Learn about Myasthenia Gravis.
- Myoclonic EpilepsyYan isExperienced. Learn about Myoclonic Epilepsy.
- Neuronal Intranuclear Inclusion Disease (NIID)
- Olivopontocerebellar Atrophy
- Pectus CarinatumYan isExperienced. Learn about Pectus Carinatum.
- Peripheral NeuropathyYan isExperienced. Learn about Peripheral Neuropathy.
- Pompe DiseaseYan isExperienced. Learn about Pompe Disease.
- Riboflavin Transporter Deficiency Neuronopathy
- Sandhoff DiseaseYan isExperienced. Learn about Sandhoff Disease.
- Sengers SyndromeYan isExperienced. Learn about Sengers Syndrome.
- Spastic Paraplegia Type 2Yan isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Yan isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityYan isExperienced. Learn about Spasticity.
- Spinal and Bulbar Muscular Atrophy
- Spinal Muscular Atrophy (SMA)
- Spinal Muscular Atrophy Type 2
- Spinal Muscular Atrophy Type 3
- Spinocerebellar AtaxiaYan isExperienced. Learn about Spinocerebellar Ataxia.
- Spinocerebellar Ataxia Type 2
- StrokeYan isExperienced. Learn about Stroke.
- Subacute Combined Degeneration
- Tay-Sachs DiseaseYan isExperienced. Learn about Tay-Sachs Disease.
- ThymectomyYan isExperienced. Learn about Thymectomy.
- Usher SyndromeYan isExperienced. Learn about Usher Syndrome.
- Vitamin B12 Deficiency Anemia