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Check Dr. Mary L. Gregory's experience treating your condition:
About Dr. Mary L. Gregory

Mary Gregory is a Neurologist and a Child Neurologist in Columbia, South Carolina. She is licensed to treat patients in South Carolina and Georgia. Gregory is currently accepting new patients.

Her clinical research consists of co-authoring 3 peer reviewed articles in the past 15 years.

Areas of Expertise

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We do not have enough information to identify the Areas of Expertise for this doctor.

          Insurance

          MediFind strives to display the most accurate insurance information for every doctor. If you do not see your insurance listed for Dr. Mary L. Gregory it is best to call her office and ask if your insurance is accepted.


          Dr. Mary L. Gregory accepts the following insurance:

          •  Blue Cross Blue Shield
          •  Ambetter
          •  Molina Healthcare
          •  Absolute Total Care

          Call to see if your plan is accepted.
          Locations
          9 Richland Medical Park Dr, Columbia, SC 29203
          Other Locations
          9 Richland Medical Park Dr, Columbia, SC 29203
          Background & Education
          Graduate Institution
          Medical University Of South Carolina College Of Medicine, 2008.0
          Specialties
          Neurology
          Child Neurology
          Licenses
          Neurology with Special Qualifications in Neurology in GA
          Hospital Affiliations
          Prisma Health Hillcrest Hospital
          Prisma Health Richland Hospital
          Languages Spoken
          English
          Gender
          Female
          Clinical Research

          Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Doctors 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.


          3 Total Publications

          A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.
          Summary: A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype.


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