Overview
Sirisak Chanprasert is a Medical Genetics provider in Seattle, Washington. Dr. Chanprasert is rated as an Advanced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. 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. In particular, he has co-authored 1 article in the study of Coenzyme Q Cytochrome C Reductase Deficiency.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- HMO
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- PPO
- INSURANCE PLAN
- MEDICARE MAPD
- OTHER COMMERCIAL
- PPO
- EPO
- HMO
- POS
- PPO
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.
Michael Bamshad is a Medical Genetics specialist and a Pediatrics provider in Seattle, Washington. Dr. Bamshad is rated as a Distinguished provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. His top areas of expertise are Distal Arthrogryposis Type 6, Distal Arthrogryposis, Arthrogryposis Multiplex Congenita, and Congenital Contractures. Dr. Bamshad is currently accepting new patients.
The Association Of University Physicians
Fuki Hisama is a Medical Genetics specialist and a Neurologist in Seattle, Washington. Dr. Hisama is rated as a Distinguished provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are Werner Syndrome, Cockayne Syndrome, Coffin-Siris Syndrome, and Cornelia De Lange Syndrome.
The Association Of University Physicians
Wendy Raskind is a Medical Genetics provider in Seattle, Washington. Dr. Raskind is rated as an Advanced provider by MediFind in the treatment of Coenzyme Q Cytochrome C Reductase Deficiency. Her top areas of expertise are Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy, Cowden Syndrome, Peutz-Jeghers Syndrome, and Hypothalamic Hamartomas. Dr. Raskind is currently accepting new patients.
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
- Fabry DiseaseDr. Chanprasert isDistinguished. Learn about Fabry Disease.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- MELAS SyndromeDr. Chanprasert isDistinguished. Learn about MELAS Syndrome.
- Multiple Sulfatase DeficiencyDr. Chanprasert isDistinguished. Learn about Multiple Sulfatase Deficiency.
- Advanced
- Coenzyme Q Cytochrome C Reductase Deficiency
- Danon DiseaseDr. Chanprasert isAdvanced. Learn about Danon Disease.
- Gaucher DiseaseDr. Chanprasert isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Chanprasert isAdvanced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Chanprasert isAdvanced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Chanprasert isAdvanced. Learn about Gaucher Disease Type 3.
- Experienced
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase DeficiencyDr. Chanprasert isExperienced. Learn about 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.
- Achalasia Microcephaly SyndromeDr. Chanprasert isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Andersen DiseaseDr. Chanprasert isExperienced. Learn about Andersen Disease.
- Argininosuccinic AciduriaDr. Chanprasert isExperienced. Learn about Argininosuccinic Aciduria.
- Cortical DysplasiaDr. Chanprasert isExperienced. Learn about Cortical Dysplasia.
- Farber LipogranulomatosisDr. Chanprasert isExperienced. Learn about Farber Lipogranulomatosis.