Overview
Sirisak Chanprasert is a Medical Genetics provider in Seattle, Washington. Dr. Chanprasert is highly rated in 17 conditions, according to our data. His top areas of expertise are MELAS Syndrome, Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, and Multiple Sulfatase Deficiency.
His clinical research consists of co-authoring 27 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Premera
Locations
1959 Ne Pacific St, Seattle, WA 98195
Additional Areas of Focus
Dr. Chanprasert has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
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.
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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.
- Distinguished
- Fabry Disease
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- MELAS Syndrome
- Multiple Sulfatase Deficiency
- Advanced
- Coenzyme Q Cytochrome C Reductase Deficiency
- Danon Disease
- Gaucher Disease
- Gaucher Disease Type 1
- Gaucher Disease Type 2
- Gaucher Disease Type 3
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- Achalasia Microcephaly Syndrome
- Andersen Disease
- Arginase Deficiency
- Argininosuccinic Aciduria
- Carbamoyl Phosphate Synthetase 1 Deficiency