Overview
Samantha Coffino is a Pediatrics provider in New York, New York. Her top areas of expertise are Mucopolysaccharidosis Type 3A (MPS IIIA, Sanfilippo Syndrome A), Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome), Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B), and VLDLR-Associated Cerebellar Hypoplasia.
Her clinical research consists of co-authoring 3 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- OTHER COMMERCIAL
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
Locations
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
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
- Experienced
- Agyria Pachygyria PolymicrogyriaDr. Coffino isExperienced. Learn about Agyria Pachygyria Polymicrogyria.
- Arthrogryposis Multiplex CongenitaDr. Coffino isExperienced. Learn about Arthrogryposis Multiplex Congenita.
- Autism Spectrum DisorderDr. Coffino isExperienced. Learn about Autism Spectrum Disorder.
- Bilateral Perisylvian PolymicrogyriaDr. Coffino isExperienced. Learn about Bilateral Perisylvian Polymicrogyria.
- Coach SyndromeDr. Coffino isExperienced. Learn about Coach Syndrome.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)