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Connection

Debopam Samanta to Male

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

 
Connection Strength
  
 
 
1.048
  
  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: 0.036
  2. Samanta D. Epilepsy in Angelman syndrome: A scoping review. Brain Dev. 2021 Jan; 43(1):32-44.
    View in: PubMed
    Score: 0.035
  3. Samanta D. Ketamine Infusion for Super Refractory Status Epilepticus in Alternating Hemiplegia of Childhood. Neuropediatrics. 2020 06; 51(3):225-228.
    View in: PubMed
    Score: 0.033
  4. Samanta D, Ramakrishnaiah R, Frye RE. Complex heterozygous polymerase gamma mutation and cerebral folate deficiency in a child with refractory partial status. Neurol India. 2019 Jan-Feb; 67(1):259-260.
    View in: PubMed
    Score: 0.031
  5. 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: 0.029
  6. 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: 0.029
  7. 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: 0.029
  8. Samanta D. Remarkable improvement of selective mutism with everolimus in a patient with tuberous sclerosis complex. Acta Neurol Belg. 2015 Dec; 115(4):815-7.
    View in: PubMed
    Score: 0.029
  9. 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: 0.029
  10. 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: 0.029
  11. Samanta D. Unilateral Cerebral Atrophy: Severe Neuroimaging Feature of Incontinentia Pigmenti without Acute Encephalopathic State. J Pediatr Neurosci. 2018 Apr-Jun; 13(2):270-272.
    View in: PubMed
    Score: 0.029
  12. Samanta D. Asymmetric photic driving response: importance of reviewing the video. Acta Neurol Belg. 2020 Apr; 120(2):395-397.
    View in: PubMed
    Score: 0.029
  13. Samanta D. E-Cigarettes and Seizures. Pediatr Neurol. 2020 04; 105:75.
    View in: PubMed
    Score: 0.029
  14. Samanta D, Beal JC, Grinspan ZM. Automated Identification of Surgical Candidates and Estimation of Postoperative Seizure Freedom in Children - A Focused Review. Semin Pediatr Neurol. 2021 10; 39:100914.
    View in: PubMed
    Score: 0.029
  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: 0.029
  16. Ramani PK, Briscoe Abath C, Donatelli S, Hadjinicolaou A, Vega Toro S, Acevedo K, Astorga KR, Parbhoo K, Singh A, Catenaccio E, Jain P, Sahu JK, Samanta D, Harini C. Initial combination versus early sequential standard therapies for Infantile Epileptic Spasms Syndrome-Feedback from stakeholders. Epilepsia Open. 2024 Apr; 9(2):819-822.
    View in: PubMed
    Score: 0.029
  17. van Eeghen AM, Thiele EA, Amin S, Samanta D, Jansen AC, Stevens J, Moore-Ramdin L, de Vries PJ. Protocol for EpiCom: A phase 3b/4 study of behavioral outcomes following adjunctive cannabidiol for the management of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND). PLoS One. 2025; 20(6):e0324648.
    View in: PubMed
    Score: 0.029
  18. 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: 0.026
  19. 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: 0.026
  20. 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: 0.026
  21. Samanta D. Sporadic hemiplegic migraine and giant tumefactive perivascular space: Is there an association? Acta Neurol Belg. 2016 Dec; 116(4):619-620.
    View in: PubMed
    Score: 0.025
  22. Samanta D. Influenza B-associated acute necrotizing encephalopathy of childhood: a report from North America. Acta Neurol Belg. 2016 Sep; 116(3):383-5.
    View in: PubMed
    Score: 0.025
  23. Samanta D. Acneiform Lesion: Importance of Detailed Skin Examination. Indian J Pediatr. 2016 May; 83(5):485-6.
    View in: PubMed
    Score: 0.025
  24. Samanta D. Osteomyelitis of bilateral great toes: iatrogenic complication of nerve conduction study. Acta Neurol Belg. 2016 Sep; 116(3):429-30.
    View in: PubMed
    Score: 0.025
  25. Samanta D. Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome. Acta Neurol Belg. 2016 Sep; 116(3):363-4.
    View in: PubMed
    Score: 0.025
  26. Samanta D. Possible Benign Partial Epilepsy. Indian Pediatr. 2015 Jul; 52(7):623.
    View in: PubMed
    Score: 0.024
  27. Samanta D. Horizontal Gaze Palsy: Additional Issues. Indian Pediatr. 2015 Jul; 52(7):624.
    View in: PubMed
    Score: 0.024
  28. Samanta D. Transient lesion in the splenium of the corpus callosum in status migrainosus. Acta Neurol Belg. 2015 Sep; 115(3):397-8.
    View in: PubMed
    Score: 0.023
  29. 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: 0.023
  30. Samanta D. Reversible cerebral vasoconstriction syndrome: another health hazard of energy drinks? Clin Pediatr (Phila). 2015 Feb; 54(2):186-7.
    View in: PubMed
    Score: 0.023
  31. Singh A, Hadjinicolaou A, Briscoe-Abath C, Donatelli S, Salussolia C, Gupta N, Almansa AS, Zhang B, Stone S, Libenson M, Samanta D, Bolton J, Harini C. Evaluating the effectiveness of medical therapy in infantile epileptic spasms syndrome due to surgically-remediable lesions. Epilepsia. 2025 May; 66(5):1433-1446.
    View in: PubMed
    Score: 0.012
  32. Mytinger JR, Albert DVF, Aylward SC, Beatty CW, Bhalla S, Bhatia S, Brock GN, Ciliberto MA, Choudhari PR, Clark DJ, Cohen JM, Czech TM, Fredwall MM, Gonzalez-Giraldo E, Harini C, Hunter SE, Sandoval Karamian AG, Katyayan A, Kistler I, Kulkarni N, Liu VB, McCabe C, Murray T, Neville K, Patel SH, Pavuluri S, Phillips DJ, Samanta D, Sirsi D, Spelbrink EM, Stafstrom CE, Steenari M, Takacs DS, Terrill T, Tran L, Vidaurre J, Shrey DW. A Multicenter Training and Interrater Reliability Study of the BASED Score for Infantile Epileptic Spasms Syndrome. J Clin Neurophysiol. 2025 Mar 01; 42(3):230-234.
    View in: PubMed
    Score: 0.011
  33. 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: 0.009
  34. Samanta D. A 15-year-old with seizures: late diagnosis of pyridoxine-dependent epilepsy. Acta Neurol Belg. 2016 Dec; 116(4):667-669.
    View in: PubMed
    Score: 0.009
  35. 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: 0.009
  36. 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: 0.009
  37. Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76.
    View in: PubMed
    Score: 0.009
  38. Samanta D. Effects of Separation on Children's Neurodevelopment. Pediatr Neurol. 2019 02; 91:72.
    View in: PubMed
    Score: 0.009
  39. Samanta D, Zarate YA. Widening phenotypic spectrum of GABBR2 mutation. Acta Neurol Belg. 2019 Sep; 119(3):493-496.
    View in: PubMed
    Score: 0.009
  40. Samanta D, Ramakrishnaiah R, Schaefer B. The neurological aspects related to POGZ mutation: case report and review of CNS malformations and epilepsy. Acta Neurol Belg. 2020 Apr; 120(2):447-450.
    View in: PubMed
    Score: 0.009
  41. Samanta D, Schaefer B. Mosaic chromosome 5p tetrasomy: eye closure-induced seizures in a rare neurocutaneous syndrome. Acta Neurol Belg. 2020 Jun; 120(3):713-716.
    View in: PubMed
    Score: 0.009
  42. Bajaj G, Lindberg MR, Chee W, Samanta D, Chhabra A. Fibroma-like PEComa: a newly recognized soft tissue neoplasm in tuberous sclerosis patients-imaging features and review of literature. Skeletal Radiol. 2022 Apr; 51(4):881-887.
    View in: PubMed
    Score: 0.009
  43. Samanta D. Pharmacotherapeutic management of seizures in patients with Angleman Syndrome. Expert Opin Pharmacother. 2022 Sep; 23(13):1511-1522.
    View in: PubMed
    Score: 0.009
  44. Zhu Z, Bolt E, Newmaster K, Osei-Bonsu W, Cohen S, Cuddapah VA, Gupta S, Paudel S, Samanta D, Dang LT, Carney PR, Naik S. SCN1B Genetic Variants: A Review of the Spectrum of Clinical Phenotypes and a Report of Early Myoclonic Encephalopathy. Children (Basel). 2022 Oct 01; 9(10).
    View in: PubMed
    Score: 0.009
  45. Zhu Z, Dluzynski D, Hammad N, Pugalenthi D, Walser SA, Mittal R, Samanta D, Brown ML, Asadi-Pooya AA, Kakooza-Mwesige A, Spalice A, Capponi M, Lekoubou A, Kumar A, Paudel S, Carney PR, Mainali G, Naik S. Use of Integrative, Complementary, and Alternative Medicine in Children with Epilepsy: A Global Scoping Review. Children (Basel). 2023 Apr 12; 10(4).
    View in: PubMed
    Score: 0.009
  46. Sullivan J, Gunning B, Zafar M, Guerrini R, Gecz J, Kolc KL, Zhao Y, Gasior M, Aimetti AA, Samanta D. Corrigendum to "Phase 2, placebo-controlled clinical study of oral ganaxolone in PCDH19-clustering epilepsy" [Epilepsy Res.?(2023) 191 107112]. Epilepsy Res. 2024 Jul; 203:107342.
    View in: PubMed
    Score: 0.009
  47. Jeno M, Zimmerman MB, Shandley S, Wong-Kisiel L, Singh RK, McNamara N, Fedak Romanowski E, Grinspan ZM, Eschbach K, Alexander A, McGoldrick P, Wolf S, Nangia S, Bolton J, Olaya J, Shrey DW, Karia S, Karakas C, Tatachar P, Ostendorf AP, Gedela S, Javarayee P, Reddy S, Manuel CM, Gonzalez-Giraldo E, Sullivan J, Coryell J, Depositario-Cabacar DFT, Hauptman JS, Samanta D, Armstrong D, Perry MS, Marashly A, Ciliberto M. Pediatric Palliative Epilepsy Surgery: A Report From the Pediatric Epilepsy Research Consortium (PERC) Surgery Database. Pediatr Neurol. 2024 Aug; 157:70-78.
    View in: PubMed
    Score: 0.009
  48. Samanta D, Haneef Z, Albert GW, Naik S, Reeders PC, Jain P, Abel TJ, Al-Ramadhani R, Ibrahim GM, Warren AEL. Neuromodulation strategies in developmental and epileptic encephalopathies. Epilepsy Behav. 2024 Nov; 160:110067.
    View in: PubMed
    Score: 0.009
  49. Theroux LM, Cappa R, Mendoza A, Mallawaarachchi I, Samanta D, Goodkin HP. Implementation of an Intravenous Dihydroergotamine Protocol for Refractory Migraine in Children. Headache. 2020 Sep; 60(8):1653-1663.
    View in: PubMed
    Score: 0.009
  50. 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: 0.008
  51. Malatesta LM, Samanta D, Ramakrishnaiah R. An Unusual Cause of Recurrent Facial Nerve Palsy. Pediatr Neurol. 2019 02; 91:68-69.
    View in: PubMed
    Score: 0.008
  52. Gabriel GK, Samanta D, Cobb S. An Unusual Holohemispheric Abnormality. Pediatr Neurol. 2019 01; 90:74-75.
    View in: PubMed
    Score: 0.008
  53. Segal MM, Williams MS, Gropman AL, Torres AR, Forsyth R, Connolly AM, El-Hattab AW, Perlman SJ, Samanta D, Parikh S, Pavlakis SG, Feldman LK, Betensky RA, Gospe SM. Evidence-based decision support for neurological diagnosis reduces errors and unnecessary workup. J Child Neurol. 2014 Apr; 29(4):487-92.
    View in: PubMed
    Score: 0.005
  54. Krishnamurthy S, Samanta D, Yadav S. Renal amyloidosis secondary to childhood tuberculosis: a report of two cases. J Postgrad Med. 2009 Apr-Jun; 55(2):121-3.
    View in: PubMed
    Score: 0.004
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.