Header Logo
Keywords
Last Name
Institution
Announcement

You can now add alternative names! Click here to add other names that you've published under.

Virginia Willis

CredentialsAmerican Board of Psychiatry and Neurology (ABPN)
ABPN Epilepsy
American Board of Clinical Neurophysiology
TitleAssociate Professor
InstitutionUniversity of Arkansas for Medical Sciences
DepartmentPeds Pediatrics, College of Medicine
DivisionPeds Neurology
Address ACH Administration
1900 Maryland Street
Mail Slot # 512-15
Little Rock AR 72202
Phone501-364-1850
vCardDownload vCard

    Collapse Overview 
    Collapse overview
    Dr. V. Erin Willis is an Associate Professor of Pediatrics in the Division of Pediatric Neurology for the University of Arkansas for Medical Sciences at Arkansas Children’s Hospital. Her clinical interests include pediatric epilepsy and demyelinating disorders.


    Collapse Affiliation 
    Collapse member of
    Child Neurology Society
    American Epilepsy Society
    National Multiple Sclerosis Society
    Consortium of Multiple Sclerosis Centers
    American Academy of Neurology
    Professors of Child Neurology

    Collapse Biography 
    Collapse Leadership and Administrative Roles
    UAMS Child Neurology Program Director

    Director of Pediatric Demyelinating Clinic

    Collapse awards and honors
    2018National MS Society Partner in Care, UAMS/Arkansas Children's Hospital

    Collapse Outreach 

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions. Don't see publications published under other names? Login to add alternative names.
    List All   |   Timeline
    1. Herrmann SD, Conger SA, Willis EA, Ainsworth BE. Promoting public health through the 2024 Compendium of Physical Activities: Strategies for adults, older adults, and wheelchair users. J Sport Health Sci. 2024 Nov; 13(6):739-742. PMID: 38825318.
      View in: PubMed
    2. Herrmann SD, Willis EA, Ainsworth BE, Barreira TV, Hastert M, Kracht CL, Schuna JM, Cai Z, Quan M, Tudor-Locke C, Whitt-Glover MC, Jacobs DR. 2024 Adult Compendium of Physical Activities: A third update of the energy costs of human activities. J Sport Health Sci. 2024 Jan; 13(1):6-12. PMID: 38242596.
      View in: PubMed
    3. Willis E, Moore SA, Cox MO, Stefans V, Aravindhan A, Gokden M, Veerapandiyan A. Limb-Girdle Muscular Dystrophy R9 due to a Novel Complex Insertion/Duplication Variant in FKRP Gene. Child Neurol Open. 2022 Jan-Dec; 9:2329048X221097518. PMID: 35557983.
      View in: PubMed
    4. Samanta D, Ostendorf AP, Willis E, Singh R, Gedela S, Arya R, Scott Perry M. Underutilization of epilepsy surgery: Part I: A scoping review of barriers. Epilepsy Behav. 2021 04; 117:107837. PMID: 33610461.
      View in: PubMed
    5. Abramo TJ, McKinney S, Moore J, Jacobs R, Albert G, Meredith M, Porter NH, Storm E, Willis E, Gonzalez CV, Hargrave H, Schneider B, Sharp G. Hemispheric Cerebral Oximetry Monitoring During Pediatric Seizure Activity in a Pediatric Emergency Department. Pediatr Emerg Care. 2020 Sep; 36(9):e513-e526. PMID: 29140931.
      View in: PubMed
    6. Lewis HS, Willis E, Veerapandiyan A. Charcot-Marie-Tooth Disease Type 4J and Multiple Sclerosis. J Clin Neuromuscul Dis. 2019 Dec; 21(2):117-118. PMID: 31743256.
      View in: PubMed
    7. Arya K, Willis E, Samanta D. Immunotherapy in Autoimmune and Neuroinflammation-related Epilepsies. J Ped Epilepsy. 2018; 7:69-75.
    8. Samanta D, Gokden M, Willis E. Clinicopathologic Findings of CARS2 Mutation. Pediatr Neurol. 2018 10; 87:65-69. PMID: 30139652.
      View in: PubMed
    9. Samanta D, Willis E. KIAA2022-related disorders can cause Jeavons (eyelid myoclonia with absence) syndrome. Acta Neurol Belg. 2020 Feb; 120(1):205-207. PMID: 29417424.
      View in: PubMed
    10. Willis E, Samanta D, Kanfi A. A Not Uncommon Cause of Stroke Mimicker in Children. Pediatr Neurol. 2018 03; 80:92-93. PMID: 29229230.
      View in: PubMed
    11. Willis E, Ramakrishnaiah R, Archer R. Neuromyelitis Optica Spectrum Disorder in a Pediatric Patient. J Ark Med Soc. 2016 Aug; 113(2):34-35. PMID: 30047629.
      View in: PubMed
    12. Samanta D, Willis E. Intractable epileptic spasms in a patient with Pontocerebellar hypoplasia: Severe phenotype of type 2 or another subtype? Ann Indian Acad Neurol. 2016 Jul-Sep; 19(3):385-7. PMID: 27570394.
      View in: PubMed
    13. Samanta D, Willis E. Focal seizure associated with human parvovirus B19 infection in a non-encephalopathic child. World J Pediatr. 2016 Feb; 12(1):118-20. PMID: 26684306.
      View in: PubMed
    14. Samanta D, Willis E. Rapid improvement of the confusional state and electroencephalography after spinal tap in a patient with headache and neurologic deficits with cerebrospinal fluid lymphocytosis (HaNDL) syndrome. Neurol India. 2015 Nov-Dec; 63(6):978-9. PMID: 26588641.
      View in: PubMed
    15. Bradley L, Bahgat D, Sharp G, Willis E, Ocal E, Albert G, Serletis D. Disconnective Hemispherotomy for Medically Intractable Status Epilepticus in an 8-Year-Old Child. J Ark Med Soc. 2015 Oct; 112(6):86-7. PMID: 26552284.
      View in: PubMed
    16. Willis E, Samanta D. Paroxysmal Nonepileptic Spells in Adolescence. Pediatr Epilepsy. 2015; 4:118-122.
    17. Samanta D, Willis E. Generalized Epilepsy Syndromes of Adolescence. J Pediatr Epilepsy. 2015; 4:36-101.
    18. Sharp GB, Samanta D, Willis E. Options for pharmacoresistant epilepsy in children: when medications don't work. Pediatr Ann. 2015 Feb; 44(2):e43-8. PMID: 25658218.
      View in: PubMed
    19. Samanta D, Willis E. Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene. Acta Neurol Belg. 2015 Dec; 115(4):779-82. PMID: 25543316.
      View in: PubMed
    20. Samanta D, Willis E, Sharp GB. Absence status after starting clobazam in a patient with syndrome of continuous spike and wave during slow sleep (CSWS). Neurol India. 2014 Nov-Dec; 62(6):685-7. PMID: 25591691.
      View in: PubMed
    21. Samanta D, Ramakrishnaiah R, Willis E, Frye RE. Myoclonic epilepsy evolved into West syndrome: a patient with a novel de novo KCNQ2 mutation. Acta Neurol Belg. 2015 Sep; 115(3):475-8. PMID: 25092550.
      View in: PubMed
    22. Willis E, Sharp G, Luat A, Maham S, Chowdury N. J Child Neurol. Subclinical seizures identified with continuous EEG monitoring in Pediatric Patients with traumatic brain injury. 2012; 27:958-964.
    Willis's Networks
    Click the "See All" links for more information and interactive visualizations!
    Concepts Expand Description
    See all (82) concept(s)
    _
    Co-Authors Expand Description
    See all (7) people
    _
    Similar People Expand Description
    See all (27) people
    _
    Same Department Expand Description
    Search Department