Overview
Lin Ge practices practicing medicine in Beijing, China.
Ge is highly rated in 6 conditions, according to our data. Their clinical expertise encompasses Fukuyama Type Muscular Dystrophy, Walker-Warburg Syndrome, Limb-Girdle Muscular Dystrophy, and Horizontal Gaze Palsy with Progressive Scoliosis.
They are actively involved in clinical research, co-authoring 45 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 Lin H. Ge
Is Lin H. Ge a top-rated expert for Fukuyama Type Muscular Dystrophy?
MediFind is an objective health platform that identifies experts based on real-world data. Lin H. Ge is classified as an Advanced expert for Fukuyama Type Muscular Dystrophy, 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 Lin H. Ge participate in research or clinical trials?
Yes. Lin H. Ge has published 45 articles and abstracts on conditions like Fukuyama Type Muscular Dystrophy. You can view a list of Lin H. Ge'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
- Fukuyama Type Muscular Dystrophy
- Horizontal Gaze Palsy with Progressive Scoliosis
- Limb-Girdle Muscular Dystrophy
- Limb-Girdle Muscular Dystrophy Type 1B
- LissencephalyGe isAdvanced. Learn about Lissencephaly.
- Walker-Warburg Syndrome
- Experienced
- Brown SyndromeGe isExperienced. Learn about Brown Syndrome.
- Centronuclear MyopathyGe isExperienced. Learn about Centronuclear Myopathy.
- Congenital Fiber-Type Disproportion
- Congenital Myasthenic Syndrome
- Cortical DysplasiaGe isExperienced. Learn about Cortical Dysplasia.
- Cramp-Fasciculation Syndrome
- EsotropiaGe isExperienced. Learn about Esotropia.
- HepatitisGe isExperienced. Learn about Hepatitis.
- Hepatitis CGe isExperienced. Learn about Hepatitis C.
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- HIV/AIDSGe isExperienced. Learn about HIV/AIDS.
- HypotoniaGe isExperienced. Learn about Hypotonia.
- Limb-Girdle Muscular Dystrophy Type 1A
- Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
- Mitochondrial Trifunctional Protein Deficiency
- Primary Lateral Sclerosis
- Protein DeficiencyGe isExperienced. Learn about Protein Deficiency.
- RhabdomyolysisGe isExperienced. Learn about Rhabdomyolysis.
- Sensorimotor Polyneuropathy
- Spinal Muscular Atrophy (SMA)
- SyphilisGe isExperienced. Learn about Syphilis.
- Tubular Aggregate Myopathy
- X-Linked Myotubular Myopathy