Overview
Raymond Wang is a Pediatrics specialist and a Medical Genetics provider in Orange, California. Dr. Wang is highly rated in 26 conditions, according to our data. 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 86 peer reviewed articles and participating in 11 clinical trials. MediFind looks at clinical research from the past 15 years.
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
Uc Regents Uci Dept Of Pediatrics
Virginia Kimonis is a Medical Genetics specialist and a Pediatrics provider in Orange, California. Dr. Kimonis is highly rated in 15 conditions, according to our data. Her top areas of expertise are Prader-Willi Syndrome, Pompe Disease, Hypotonia, Fabry Disease, and Hormone Replacement Therapy (HRT).
Matthew Deardorff is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Deardorff is highly rated in 28 conditions, according to our data. His top areas of expertise are Cornelia De Lange Syndrome, Coffin-Siris Syndrome, Mosaicism, and Beckwith-Wiedemann Syndrome.
Uc Regents
Nicola Longo is a Medical Genetics specialist and a Pediatrics provider in Los Angeles, California. Dr. Longo has been practicing medicine for over 43 years is highly rated in 29 conditions, according to our data. His top areas of expertise are Primary Carnitine Deficiency, Gaucher Disease Type 1, Urea Cycle Disorders (UCD), and Phenylketonuria (PKU). Dr. Longo is currently accepting new patients.
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
- Beta-Ketothiolase Deficiency
- Brachydactyly Mononen Type
- Fabry Disease
- GM1 Gangliosidosis
- Hereditary Coproporphyria
- Increased Head Circumference
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)
- ALG1-CDG
- Alpha Thalassemia
- Cortical Dysplasia
- Epilepsy in Children
- Fetal Edema