Overview
Michael Luceri is a Pediatrics specialist and a Pediatric Cardiologist in Wilmington, Delaware. Dr. Luceri is rated as an Experienced provider by MediFind in the treatment of Neu Laxova Syndrome. His top areas of expertise are Familial Neurocardiogenic Syncope, Fainting, Heart Murmurs, and Patent Ductus Arteriosus.
His clinical research consists of co-authoring 2 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
- EPO
- HMO
- PPO
- EPO
- POS
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- MEDICARE MAPD
- MEDICARE SNP
- OTHER MEDICARE PART D
- POS
- EPO
- HMO
- POS
- PPO
- EPO
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
1600 Rockland Road, Nemours Cardiac Center, Wilmington, DE 19803
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.
Dena Matalon is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Matalon is rated as a Distinguished provider by MediFind in the treatment of Neu Laxova Syndrome. Her top areas of expertise are Campomelia Cumming Type, Coffin-Lowry Syndrome, Microcephaly Deafness Syndrome, and Nevoid Basal Cell Carcinoma Syndrome.
Mahim Jain is a Medical Genetics specialist and a Pediatrics provider in Wilmington, Delaware. Dr. Jain is rated as a Distinguished provider by MediFind in the treatment of Neu Laxova Syndrome. His top areas of expertise are Osteogenesis Imperfecta, Spondyloepimetaphyseal Dysplasia Strudwick Type, Miller-Dieker Syndrome, and Lissencephaly 1. Dr. Jain is currently accepting new patients.
Center For Medical Genomics Office HGCC MDC
Nina Powell is a Pediatrics specialist and a Medical Genetics provider in Newark, Delaware. Dr. Powell is rated as an Advanced provider by MediFind in the treatment of Neu Laxova Syndrome. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Increased Head Circumference, and Megalencephaly-Capillary Malformation 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
- Bicuspid Aortic ValveDr. Luceri isAdvanced. Learn about Bicuspid Aortic Valve.
- Coarctation of the AortaDr. Luceri isAdvanced. Learn about Coarctation of the Aorta.
- Double Aortic ArchDr. Luceri isAdvanced. Learn about Double Aortic Arch.
- FaintingDr. Luceri isAdvanced. Learn about Fainting.
- Familial Dilated CardiomyopathyDr. Luceri isAdvanced. Learn about Familial Dilated Cardiomyopathy.
- Familial DysautonomiaDr. Luceri isAdvanced. Learn about Familial Dysautonomia.
- Experienced
- Aase SyndromeDr. Luceri isExperienced. Learn about Aase Syndrome.
- Aberrant Subclavian ArteryDr. Luceri isExperienced. Learn about Aberrant Subclavian Artery.
- Abruzzo-Erickson SyndromeDr. Luceri isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acrodermatitis EnteropathicaDr. Luceri isExperienced. Learn about Acrodermatitis Enteropathica.
- Acrorenal Mandibular SyndromeDr. Luceri isExperienced. Learn about Acrorenal Mandibular Syndrome.
- Adenosine Deaminase 2 DeficiencyDr. Luceri isExperienced. Learn about Adenosine Deaminase 2 Deficiency.
