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Amy L. McGregor, MD

Assistant Professor
Department of Neurology and Pediatrics

The University of Tennessee Health Science Center
Pediatric Neurology
777 Washington Ave. Suite 335
Memphis, TN 38105
Phone: 901.287.5208
Fax: 901.287.5325
Email: Amy L. McGregor

Education

  • MD Institution: Washington University School of Medicine
  • Residency: Pediatrics and Child Neurology - Houston Medical School
  • Fellowship: Clinical Neurophysiology, University of Texas - Houston Medical School

Research Interests

Epilepsy

Representative Publications

  • Rossi GC, Patterson AL, McGregor AL, Wheless JW. Intractable Generalized Epilepsy and Autosomal Dominant Hypocalcemia: A Case Report. Child Neurol Open. 2019 Sep 19;6:2329048X19876199. doi: 10.1177/2329048X19876199. eCollection 2019. PubMed PMID: 31763346; PubMed Central PMCID: PMC6852356.
  • Fulton SP, Van Poppel K, McGregor AL, Mudigoudar B, Wheless JW. Vagus Nerve Stimulation in Intractable Epilepsy Associated With SCN1A Gene Abnormalities. J Child Neurol. 2017 Apr;32(5):494-498. doi: 10.1177/0883073816687221. Epub 2017 Jan 12. PubMed PMID: 28079431.
  • Patterson AL, Mudigoudar B, Fulton S, McGregor A, Poppel KV, Wheless MC, Brooks L, Wheless JW. SmartWatch by SmartMonitor: Assessment of Seizure Detection Efficacy for Various Seizure Types in Children, a Large Prospective Single-Center Study. Pediatr Neurol. 2015 Oct;53(4):309-11. doi: 10.1016/j.pediatrneurol.2015.07.002. Epub 2015 Jul 15. PubMed PMID: 26272007.
  • Choudhri AF, Whitehead MT, McGregor AL, Einhaus SL, Boop FA, Wheless JW. Diffusion tensor imaging to evaluate commissural disconnection after corpus callosotomy. Neuroradiology. 2013 Nov;55(11):1397-403. doi: 10.1007/s00234-013-1286-y. Epub 2013 Oct 10. PubMed PMID: 24113714.
  • Boop S, Wheless J, Van Poppel K, McGregor A, Boop FA. Cerebellar seizures. J Neurosurg Pediatr. 2013 Sep;12(3):288-92. doi: 10.3171/2013.5.PEDS1394. Epub 2013 Jun 28. PubMed PMID: 23808728.
  • Van Poppel K, Patay Z, Roberts D, Clarke D, McGregor A, Perkins FF, Wheless J. Authors' response to correspondence on "mesial temporal sclerosis in a cohort of children with SCN1A gene mutation". J Child Neurol. 2013 Apr;28(4):542. doi: 10.1177/0883073812473509. PubMed PMID: 23504253.

View more references (pubmed link)

Last Published: Apr 19, 2021