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 Delayed Growth. 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.
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.
Yechiel Zagelbaum is a Pediatrics provider in Brooklyn, New York. Dr. Zagelbaum is rated as an Advanced provider by MediFind in the treatment of Delayed Growth. His top areas of expertise are Chickenpox, Croup, Herpangina, and Obesity in Children.
Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider in New Hyde Park, New York. Dr. Fernandes is rated as an Advanced provider by MediFind in the treatment of Delayed Growth. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Acrodermatitis Enteropathica, and CHARGE Syndrome.
Cohen Children's Northwell Health Physician Partners Medical Genetics
Dr. Ian Daniel Krantz, MD, is a renowned physician specializing in Genetics and Pediatrics. He currently sees patients at Cohen Children's Medical Center (CCMC) and Northwell Health Physician Partners Medical Genetics. Dr. Krantz holds certifications in Clinical Genetics, Cytogenetics, and Pediatrics from the American Board of Medical Genetics and the American Board of Pediatrics, respectively.Dr. Krantz completed his BFA at Concordia University in Montreal and his MD at Sackler School of Medicine (Tel Aviv University). He completed his residency in Medical Genetics at Children's Hospital of Philadelphia and his residency in Pediatrics at New York University Medical Center.With an impressive set of academic and administrative titles, Dr. Krantz serves as the Division Chief of Pediatric Genetics and Genomics at Cohen Children's Medical Center and is the System Vice President for Pediatric Genetics at Northwell Health. Additionally, he holds the position of Professor at the Zucker School of Medicine at Northwell Health.Dr. Krantz is recognized for his clinical expertise in isolated and syndromic forms of congenital birth differences and developmental diagnoses, including syndromic and non-syndromic autism. He has a special interest in the genetics of hearing loss and focused expertise in Cornelia de Lange Syndrome, Pallister-Killian syndrome, Alagille syndrome, CHOPS syndrome, among others.Dr. Krantz's research is dedicated to identifying and characterizing the molecular etiology of syndromic and non-syndromic developmental diagnoses. His research lab has made significant contributions in the field, discovering new disease genes and shedding light on critical molecular pathways involved in human developmental disorders.Driven by his commitment to advancing patient care, Dr. Krantz has been at the forefront of integrating genomic technologies into the clinical setting. He has implemented rapid genome sequencing into the NICU and CICU and established biobanks and biorepositories to further research efforts. Through his work, he aims to understand the impact of complex diagnostic information on clinicians and families involved.With his extensive expertise and dedication to advancing genetic research and patient care, Dr. Krantz continues to make significant contributions to the field of Pediatrics and Genetics. Dr. Krantz is rated as a Distinguished provider by MediFind in the treatment of Delayed Growth. His top areas of expertise are Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.
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.

