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This is a "connection" page, showing publications co-authored by Debopam Samanta and Virginia Willis.

Connection Strength
  1. Samanta D, Gokden M, Willis E. Clinicopathologic Findings of CARS2 Mutation. Pediatr Neurol. 2018 10; 87:65-69.
    View in: PubMed
    Score: 0.671
  2. Samanta D, Willis E. KIAA2022-related disorders can cause Jeavons (eyelid myoclonia with absence) syndrome. Acta Neurol Belg. 2020 Feb; 120(1):205-207.
    View in: PubMed
    Score: 0.653
  3. 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.
    View in: PubMed
    Score: 0.584
  4. 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.
    View in: PubMed
    Score: 0.563
  5. 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.
    View in: PubMed
    Score: 0.558
  6. 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.
    View in: PubMed
    Score: 0.526
  7. 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.
    View in: PubMed
    Score: 0.201
  8. Willis E, Samanta D, Kanfi A. A Not Uncommon Cause of Stroke Mimicker in Children. Pediatr Neurol. 2018 03; 80:92-93.
    View in: PubMed
    Score: 0.161
  9. 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.
    View in: PubMed
    Score: 0.132
  10. 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.
    View in: PubMed
    Score: 0.130
  11. 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.
    View in: PubMed
    Score: 0.128
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.