Overview
Raymond Wang is a Pediatrics specialist and a Medical Genetics provider in Orange, California. Dr. Wang and is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), and Pompe Disease.
His clinical research consists of co-authoring 91 peer reviewed articles and participating in 11 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).
Insurance
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Locations
1201 W La Veta Ave, Orange, CA 92868
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers 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.
11 Clinical Trials
Lynda Polgreen is a Pediatric Endocrinologist and a Pediatrics provider in Orange, California. Dr. Polgreen and is rated as a Distinguished provider by MediFind in the treatment of Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). Her top areas of expertise are Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Osteopetrosis, Mucopolysaccharidoses (MPS), Osteosclerosis Autosomal Dominant, and Osteotomy.
Childrens Hospital Los Angeles Medical Group Inc
Linda Randolph is a Medical Genetics provider in Los Angeles, California. Dr. Randolph has been practicing medicine for over 43 years and is rated as an Advanced provider by MediFind in the treatment of Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome). Her top areas of expertise are Trisomy 13, Chromosome 13q Duplication, Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome), and Chromosome 11 Uniparental Disomy.
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the 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.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Elite
- Mucopolysaccharidoses (MPS)
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome)
- Pompe Disease
- Advanced
- Brachydactyly Mononen Type
- Fabry Disease
- Gangliosidosis
- GM1 Gangliosidosis
- Hereditary Coproporphyria
- Increased Head Circumference
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)
- ALG1-CDG
- Alpha Thalassemia
- Beta-Ketothiolase Deficiency
- Cortical Dysplasia
- Epilepsy in Children