Overview
Sirisak Chanprasert is a Medical Genetics provider practicing medicine in Seattle, Washington.
Dr. Chanprasert is highly rated in 15 conditions, according to our data. His clinical expertise encompasses MELAS Syndrome, Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, and Multiple Sulfatase Deficiency.
He is actively involved in clinical research, co-authoring 29 peer reviewed articles. Dr. Chanprasert is currently accepting new patients.
Specialties
Licenses
Hospital Affiliations
Languages Spoken
Gender
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.
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Frequently Asked Questions about Dr. Sirisak Chanprasert
How do I make an appointment with Dr. Sirisak Chanprasert?
You can book an appointment with Dr. Sirisak Chanprasert by calling their office at 206-598-4333. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Sirisak Chanprasert a top-rated expert for MELAS Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Sirisak Chanprasert is classified as an Distinguished expert for MELAS Syndrome, 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.
What conditions does Dr. Sirisak Chanprasert specialize in?
While Dr. Sirisak Chanprasert is a Medical Genetics, they have specific expertise in MELAS Syndrome, Fabry Disease, and Megalencephalic Leukoencephalopathy with Subcortical Cysts. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Sirisak Chanprasert participate in research or clinical trials?
Yes. Dr. Sirisak Chanprasert has published 29 articles and abstracts on conditions like MELAS Syndrome. You can view a list of Dr. Sirisak Chanprasert's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Sirisak Chanprasert accept my insurance?
Dr. Sirisak Chanprasert accepts most major insurance plans, including Aetna and Cambia Health Solutions. We recommend calling the office directly at 206-598-4333 to verify that your specific plan is currently accepted before your visit.
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.
- Glutaric Acidemia Type 2Dr. Chanprasert isAdvanced. Learn about Glutaric Acidemia Type 2.
- Kearns-Sayre SyndromeDr. Chanprasert isAdvanced. Learn about Kearns-Sayre Syndrome.
- Mitochondrial Complex 1 DeficiencyDr. Chanprasert isAdvanced. Learn about Mitochondrial Complex 1 Deficiency.
- Mitochondrial Trifunctional Protein Deficiency
- Pompe DiseaseDr. Chanprasert isAdvanced. Learn about Pompe Disease.
- 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.
- Hypomelanosis of ItoDr. Chanprasert isExperienced. Learn about Hypomelanosis of Ito.
- HypospadiasDr. Chanprasert isExperienced. Learn about Hypospadias.
- HypotoniaDr. Chanprasert isExperienced. Learn about Hypotonia.
- Inborn Amino Acid Metabolism DisorderDr. Chanprasert isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Increased Head CircumferenceDr. Chanprasert isExperienced. Learn about Increased Head Circumference.
- LeukodystrophyDr. Chanprasert isExperienced. Learn about Leukodystrophy.
- Maple Syrup Urine DiseaseDr. Chanprasert isExperienced. Learn about Maple Syrup Urine Disease.
- Menkes DiseaseDr. Chanprasert isExperienced. Learn about Menkes Disease.
- MicrocephalyDr. Chanprasert isExperienced. Learn about Microcephaly.
- Mucopolysaccharidoses (MPS)Dr. Chanprasert isExperienced. Learn about Mucopolysaccharidoses (MPS).
- NeurofibromatosisDr. Chanprasert isExperienced. Learn about Neurofibromatosis.
- Occipital Horn SyndromeDr. Chanprasert isExperienced. Learn about Occipital Horn Syndrome.
- Pelizaeus-Merzbacher DiseaseDr. Chanprasert isExperienced. Learn about Pelizaeus-Merzbacher Disease.
- Phenylketonuria (PKU)Dr. Chanprasert isExperienced. Learn about Phenylketonuria (PKU).
- Progressive External OphthalmoplegiaDr. Chanprasert isExperienced. Learn about Progressive External Ophthalmoplegia.
- SplenomegalyDr. Chanprasert isExperienced. Learn about Splenomegaly.
- Undescended TesticleDr. Chanprasert isExperienced. Learn about Undescended Testicle.
- Urea Cycle Disorders (UCD)Dr. Chanprasert isExperienced. Learn about Urea Cycle Disorders (UCD).
- X-Linked Retinitis Pigmentosa (XLRP)Dr. Chanprasert isExperienced. Learn about X-Linked Retinitis Pigmentosa (XLRP).