Overview
Patricia Galvin-Parton is a Medical Genetics specialist and a Pediatrics provider in Islip Terrace, New York. Dr. Galvin-Parton is rated as an Experienced provider by MediFind in the treatment of Rommen Mueller Sybert Syndrome. Her top areas of expertise are Phenylketonuria (PKU), Krabbe Disease, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.
Her clinical research consists of co-authoring 6 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Rommen Mueller Sybert Syndrome.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE PART D
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
2701 Sunrise Hwy, Islip Terrace, NY 11752
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.
Beth Pletcher is a Medical Genetics specialist and a Pediatrics provider in Newark, New Jersey. Dr. Pletcher is rated as an Advanced provider by MediFind in the treatment of Rommen Mueller Sybert Syndrome. Her top areas of expertise are Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant, Dyggve-Melchior-Clausen Syndrome, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, and Gastrostomy.
Advantage Care Diagnostic And Treatment Center Inc
Mary Mulqueen is a primary care provider, practicing in Pediatrics and Internal Medicine in Glen Head, New York. Dr. Mulqueen is rated as an Advanced provider by MediFind in the treatment of Rommen Mueller Sybert Syndrome. Her top areas of expertise are Down Syndrome, Autism Spectrum Disorder, Fragile XE Syndrome, and Fragile X Syndrome.
Winthrop Faculty Medical Affiliates University Faculty Practice Corpor
Paul Saenger is a Pediatrics provider in Mineola, New York. Dr. Saenger is rated as a Distinguished provider by MediFind in the treatment of Rommen Mueller Sybert Syndrome. His top areas of expertise are Pediatric Growth Hormone Deficiency, Growth Hormone Deficiency (GHD), Small for Gestational Age, and Short Stature (Growth Disorders).
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
- Advanced
- Dihydropteridine Reductase DeficiencyDr. Galvin-Parton isAdvanced. Learn about Dihydropteridine Reductase Deficiency.
- Krabbe DiseaseDr. Galvin-Parton isAdvanced. Learn about Krabbe Disease.
- Maternal HyperphenylalaninemiaDr. Galvin-Parton isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Phenylketonuria (PKU)Dr. Galvin-Parton isAdvanced. Learn about Phenylketonuria (PKU).
- Experienced
- Achalasia Microcephaly SyndromeDr. Galvin-Parton isExperienced. Learn about Achalasia Microcephaly Syndrome.
- AminoaciduriaDr. Galvin-Parton isExperienced. Learn about Aminoaciduria.
- Beta-Ketothiolase DeficiencyDr. Galvin-Parton isExperienced. Learn about Beta-Ketothiolase Deficiency.
- Chromosome 11 Uniparental DisomyDr. Galvin-Parton isExperienced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 2 Uniparental DisomyDr. Galvin-Parton isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- Chromosome 6 Uniparental DisomyDr. Galvin-Parton isExperienced. Learn about Chromosome 6 Uniparental Disomy.