Overview
Debra Regier is a Pediatrics specialist and a Medical Genetics provider in Charlotte, North Carolina. Dr. Regier is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Her top areas of expertise are Gangliosidosis, GM1 Gangliosidosis, Cantu Syndrome, and Maple Syrup Urine Disease.
Her clinical research consists of co-authoring 46 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
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- EPO
- POS
- PPO
- HMO
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE-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
- HMO
- POS
- PPO
Locations
1001 Blythe Blvd, Charlotte, NC 28203
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.
Atrium Health Levine Children's Genetics
Edwin Ferren is a Pediatrics specialist and a Medical Genetics provider in Charlotte, North Carolina. Dr. Ferren is rated as an Experienced provider by MediFind in the treatment of Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. His top areas of expertise are Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, Pyruvate Decarboxylase Deficiency, and Gastrostomy. Dr. Ferren is currently accepting new patients.
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
- Cantu SyndromeDr. Regier isDistinguished. Learn about Cantu Syndrome.
- GangliosidosisDr. Regier isDistinguished. Learn about Gangliosidosis.
- GM1 GangliosidosisDr. Regier isDistinguished. Learn about GM1 Gangliosidosis.
- Advanced
- Glutaric Acidemia Type 1Dr. Regier isAdvanced. Learn about Glutaric Acidemia Type 1.
- HyperlysinemiaDr. Regier isAdvanced. Learn about Hyperlysinemia.
- Malonyl-CoA Decarboxylase Deficiency
- Maple Syrup Urine DiseaseDr. Regier isAdvanced. Learn about Maple Syrup Urine Disease.
- Phenylketonuria (PKU)Dr. Regier isAdvanced. Learn about Phenylketonuria (PKU).
- Tay-Sachs DiseaseDr. Regier isAdvanced. Learn about Tay-Sachs Disease.
- Experienced
- Adrenoleukodystrophy (ALD)Dr. Regier isExperienced. Learn about Adrenoleukodystrophy (ALD).
- AlkaptonuriaDr. Regier isExperienced. Learn about Alkaptonuria.
- Autism Spectrum DisorderDr. Regier isExperienced. Learn about Autism Spectrum Disorder.
- Beckwith-Wiedemann SyndromeDr. Regier isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- BrachydactylyDr. Regier isExperienced. Learn about Brachydactyly.
- Brachydactyly Mononen TypeDr. Regier isExperienced. Learn about Brachydactyly Mononen Type.