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Connection

Debopam Samanta to Infant

This is a "connection" page, showing publications Debopam Samanta has written about Infant.

 
Connection Strength
 
 
 
1.248
 
  1. Samanta D, Ramakrishnaiah R. Intravenous Immunoglobulin in the Treatment of Alternating Hemiplegia of Childhood. Clin Neuropharmacol. 2021 Jan-Feb 01; 44(1):23-26.
    View in: PubMed
    Score: 0.104
  2. Samanta D. Improving Management of Infantile Spasms by Adopting Implementation Science. Neuropediatrics. 2020 12; 51(6):377-388.
    View in: PubMed
    Score: 0.102
  3. Samanta D. Epilepsy in Angelman syndrome: A scoping review. Brain Dev. 2021 Jan; 43(1):32-44.
    View in: PubMed
    Score: 0.101
  4. Samanta D, Gokden M. PEHO syndrome: KIF1A mutation and decreased activity of mitochondrial respiratory chain complex. J Clin Neurosci. 2019 Mar; 61:298-301.
    View in: PubMed
    Score: 0.089
  5. Samanta D. Asymmetric photic driving response: importance of reviewing the video. Acta Neurol Belg. 2020 Apr; 120(2):395-397.
    View in: PubMed
    Score: 0.088
  6. Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76.
    View in: PubMed
    Score: 0.088
  7. Samanta D. Epileptic spasm and de novo KCNB1 mutation: if it is not one potassium channel, it is another! Acta Neurol Belg. 2020 Apr; 120(2):417-420.
    View in: PubMed
    Score: 0.086
  8. Samanta D. Contactin-associated protein-like (CNTNAP) 2 gene mutation in a patient with bilateral schizencephaly. Acta Neurol Belg. 2017 03; 117(1):403-404.
    View in: PubMed
    Score: 0.075
  9. Samanta D. Infantile spasms in Williams-Beuren syndrome with typical deletions of the 7q11.23 critical region and a review of the literature. Acta Neurol Belg. 2017 03; 117(1):359-362.
    View in: PubMed
    Score: 0.075
  10. Samanta D, Bosanko KB, Zarate YA. An infant with ash-leaf and caf? au lait spots: a case of double phakomatosis. Acta Neurol Belg. 2017 03; 117(1):323-324.
    View in: PubMed
    Score: 0.075
  11. Samanta D. Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy. Neurol India. 2016 Mar-Apr; 64(2):327-8.
    View in: PubMed
    Score: 0.074
  12. Samanta D. Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation. Acta Neurol Belg. 2016 Jun; 116(2):223-4.
    View in: PubMed
    Score: 0.071
  13. Samanta D, Ramakrishnaiah R. De novo R853Q mutation of SCN2A gene and West syndrome. Acta Neurol Belg. 2015 Dec; 115(4):773-6.
    View in: PubMed
    Score: 0.069
  14. 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: 0.066
  15. Buijsse N, Jansen FE, Ockeloen CW, van Kempen MJA, Zeidler S, Willemsen MH, Scarano E, Monticone S, Zonneveld-Huijssoon E, Low KJ, Bayat A, Sisodiya SM, Samanta D, Lesca G, de Jong D, Giltay JC, Verbeek NE, Kleefstra T, Brilstra EH, Vlaskamp DRM. Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome. Epilepsia Open. 2023 Dec; 8(4):1300-1313.
    View in: PubMed
    Score: 0.031
  16. Yuskaitis CJ, Mytinger JR, Baumer FM, Zhang B, Liu S, Samanta D, Hussain SA, Yozawitz EG, Keator CG, Joshi C, Singh RK, Bhatia S, Bhalla S, Shellhaas R, Harini C. Association of Time to Clinical Remission With Sustained Resolution in Children With New-Onset Infantile Spasms. Neurology. 2022 11 29; 99(22):e2494-e2503.
    View in: PubMed
    Score: 0.029
  17. Lewis H, Samanta D, ?rsell JL, Bosanko KA, Rowell A, Jones M, Dale RC, Taravath S, Hahn CD, Krishnakumar D, Chagnon S, Keller S, Hagebeuk E, Pathak S, Bebin EM, Arndt DH, Alexander JJ, Mainali G, Coppola G, Maclean J, Sparagana S, McNamara N, Smith DM, Raggio V, Cruz M, Fern?ndez-Ja?n A, Kava MP, Emrick L, Fish JL, Vanderver A, Helman G, Pierson TM, Zarate YA. Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated Syndrome. Pediatr Neurol. 2020 11; 112:94-100.
    View in: PubMed
    Score: 0.025
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.