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Debopam Samanta

TitleAssociate Professor
InstitutionUniversity of Arkansas for Medical Sciences
DepartmentPediatrics, College of Medicine
DivisionPeds Neurology
AddressS4175 ACH Sturgis Building
1900 Maryland Street
Mail Slot # 512-15
Little Rock AR 72202
Phone501-364-5281
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    Collapse Bibliographic 
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    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.
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    1. Samanta D. Levetiracetam is Still Not a First-line Treatment in Neonatal Seizures. Indian Pediatr. 2020 01 15; 57(1):80. PMID: 31937712.
      View in: PubMed
    2. Samanta D. Rhizomelic chondrodysplasia punctata: Role of EEG as a biomarker of impending epilepsy. eNeurologicalSci. 2020 Mar; 18:100218. PMID: 31853509.
      View in: PubMed
    3. Samanta D. Ketamine in Refractory Neonatal Seizures. Pediatr Neurol. 2019 Nov 29. PMID: 31917102.
      View in: PubMed
    4. Samanta D. Management of Alternating Hemiplegia of Childhood: A Review. Pediatr Neurol. 2019 Nov 01. PMID: 31836335.
      View in: PubMed
    5. Harada Y, Ramakrishnaiah R, Arya K, Samanta D. Extensive reversible myelopathy secondary to acute quadriventricular noncommunicating hydrocephalus. Childs Nerv Syst. 2019 Nov; 35(11):2023-2026. PMID: 31375904.
      View in: PubMed
    6. Samanta D, Schaefer B. Mosaic chromosome 5p tetrasomy: eye closure-induced seizures in a rare neurocutaneous syndrome. Acta Neurol Belg. 2019 Jul 10. PMID: 31292937.
      View in: PubMed
    7. Samanta D, Cobb S, Arya K. Sneddon Syndrome: A Comprehensive Overview. J Stroke Cerebrovasc Dis. 2019 Aug; 28(8):2098-2108. PMID: 31160219.
      View in: PubMed
    8. Samanta D, Ramakrishnaiah R. Recurrent Oral Ulcers in a Child With Seizures. Pediatr Neurol. 2019 Apr 25. PMID: 31122835.
      View in: PubMed
    9. Samanta D. Cannabidiol: A Review of Clinical Efficacy and Safety in Epilepsy. Pediatr Neurol. 2019 07; 96:24-29. PMID: 31053391.
      View in: PubMed
    10. 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. 2019 Mar 16. PMID: 30879264.
      View in: PubMed
    11. Samanta D, Ramakrishnaiah R, Crary SE, Sukumaran S, Burrow TA. Multiple Autoimmune Disorders in Aicardi-Goutières Syndrome. Pediatr Neurol. 2019 07; 96:37-39. PMID: 30898416.
      View in: PubMed
    12. Samanta D, Zarate YA. Widening phenotypic spectrum of GABBR2 mutation. Acta Neurol Belg. 2019 Sep; 119(3):493-496. PMID: 30707408.
      View in: PubMed
    13. Samanta D. A Girl with Palpitations and Periodic Weakness. Indian J Pediatr. 2019 05; 86(5):480. PMID: 30656561.
      View in: PubMed
    14. 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. PMID: 30860128.
      View in: PubMed
    15. Samanta D, Ramakrishnaiah R. Recurrent Encephalopathy with Spinal Cord Involvement: An Atypical Manifestation of Aicardi-Goutières Syndrome. Ann Indian Acad Neurol. 2019 Jan-Mar; 22(1):111-115. PMID: 30692772.
      View in: PubMed
    16. Samanta D. Reply to Cerebral Infarction in CARS2 Mutation. Pediatr Neurol. 2019 04; 93:66. PMID: 30686629.
      View in: PubMed
    17. Samanta D. Headaches in Loyes-Dietz Syndrome. J Child Neurol. 2018 Dec 19; 883073818815039. PMID: 30565496.
      View in: PubMed
    18. Samanta D, Gokden M. PEHO syndrome: KIF1A mutation and decreased activity of mitochondrial respiratory chain complex. J Clin Neurosci. 2019 Mar; 61:298-301. PMID: 30385166.
      View in: PubMed
    19. Malatesta LM, Samanta D, Ramakrishnaiah R. An Unusual Cause of Recurrent Facial Nerve Palsy. Pediatr Neurol. 2019 02; 91:68-69. PMID: 30471898.
      View in: PubMed
    20. Samanta D. Effects of Separation on Children's Neurodevelopment. Pediatr Neurol. 2019 02; 91:72. PMID: 30471897.
      View in: PubMed
    21. Samanta D, Alvarez-Nunez F. Mass-Like Lesion on Brain Magnetic Resonance Imaging. Pediatr Neurol. 2018 12; 89:71-72. PMID: 30396829.
      View in: PubMed
    22. Gabriel GK, Samanta D, Cobb S. An Unusual Holohemispheric Abnormality. Pediatr Neurol. 2019 01; 90:74-75. PMID: 30420108.
      View in: PubMed
    23. Samanta D. Asymmetric photic driving response: importance of reviewing the video. Acta Neurol Belg. 2018 Sep 01. PMID: 30173312.
      View in: PubMed
    24. Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76. PMID: 30327240.
      View in: PubMed
    25. Samanta D, Gokden M, Willis E. Clinicopathologic Findings of CARS2 Mutation. Pediatr Neurol. 2018 10; 87:65-69. PMID: 30139652.
      View in: PubMed
    26. Samanta D. Epileptic spasm and de novo KCNB1 mutation: if it is not one potassium channel, it is another! Acta Neurol Belg. 2018 May 28. PMID: 29808309.
      View in: PubMed
    27. 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. PMID: 30090155.
      View in: PubMed
    28. Samanta D, Willis E. KIAA2022-related disorders can cause Jeavons (eyelid myoclonia with absence) syndrome. Acta Neurol Belg. 2018 Feb 07. PMID: 29417424.
      View in: PubMed
    29. 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
    30. Samanta D. Surendra Nath Sehgal: A pioneer in rapamycin discovery. Indian J Cancer. 2017 Oct-Dec; 54(4):697-698. PMID: 30082562.
      View in: PubMed
    31. Samanta D, Ramakrishnaiah R. Diffuse Carotid Arteriosclerosis and Stroke in a Patient With Schimke Immuno-osseous Dysplasia. Pediatr Neurol. 2017 Jun; 71:82-83. PMID: 28412018.
      View in: PubMed
    32. 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
    33. 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. PMID: 27233939.
      View in: PubMed
    34. 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. PMID: 27062269.
      View in: PubMed
    35. Samanta D, Bosanko KB, Zarate YA. An infant with ash-leaf and café au lait spots: a case of double phakomatosis. Acta Neurol Belg. 2017 03; 117(1):323-324. PMID: 27043227.
      View in: PubMed
    36. Samanta D. A 15-year-old with seizures: late diagnosis of pyridoxine-dependent epilepsy. Acta Neurol Belg. 2016 Dec; 116(4):667-669. PMID: 26943461.
      View in: PubMed
    37. Samanta D. Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy. Neurol India. 2016 Mar-Apr; 64(2):327-8. PMID: 26954813.
      View in: PubMed
    38. Samanta D, Gokden M, Albert GW. Absence of seizures in Rasmussen encephalitis with active inflammation. J Clin Neurosci. 2016 Jun; 28:175-8. PMID: 26775150.
      View in: PubMed
    39. Samanta D. Sporadic hemiplegic migraine and giant tumefactive perivascular space: Is there an association? Acta Neurol Belg. 2016 Dec; 116(4):619-620. PMID: 26696413.
      View in: PubMed
    40. 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
    41. Samanta D. Influenza B-associated acute necrotizing encephalopathy of childhood: a report from North America. Acta Neurol Belg. 2016 Sep; 116(3):383-5. PMID: 26627900.
      View in: PubMed
    42. Samanta D. Acneiform Lesion: Importance of Detailed Skin Examination. Indian J Pediatr. 2016 May; 83(5):485-6. PMID: 26558921.
      View in: PubMed
    43. 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
    44. Samanta D. Osteomyelitis of bilateral great toes: iatrogenic complication of nerve conduction study. Acta Neurol Belg. 2016 Sep; 116(3):429-30. PMID: 26498128.
      View in: PubMed
    45. Samanta D. Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome. Acta Neurol Belg. 2016 Sep; 116(3):363-4. PMID: 26476657.
      View in: PubMed
    46. Samanta D. Topical mTOR (mechanistic target of rapamycin) inhibitor therapy in facial angiofibroma. Indian J Dermatol Venereol Leprol. 2015 Sep-Oct; 81(5):540-1. PMID: 26323682.
      View in: PubMed
    47. Samanta D. A Girl With "Weakness": Can Hyperventilation From Crying Give a Clue to the Diagnosis? Pediatr Neurol. 2016 Jan; 54:95-6. PMID: 26454327.
      View in: PubMed
    48. 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. PMID: 26280111.
      View in: PubMed
    49. Samanta D. Dry beriberi preceded Wernicke's encephalopathy: Thiamine deficiency after laparoscopic sleeve gastrectomy. J Pediatr Neurosci. 2015 Jul-Sep; 10(3):297-9. PMID: 26557183.
      View in: PubMed
    50. Samanta D. Possible Benign Partial Epilepsy. Indian Pediatr. 2015 Jul; 52(7):623. PMID: 26244962.
      View in: PubMed
    51. Samanta D. Horizontal Gaze Palsy: Additional Issues. Indian Pediatr. 2015 Jul; 52(7):624. PMID: 26244964.
      View in: PubMed
    52. 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. PMID: 25784638.
      View in: PubMed
    53. Samanta D, Ramakrishnaiah R. De novo R853Q mutation of SCN2A gene and West syndrome. Acta Neurol Belg. 2015 Dec; 115(4):773-6. PMID: 25772804.
      View in: PubMed
    54. Samanta D. Changing landscape of child neurology practice. Pediatr Neurol. 2015 Jun; 52(6):e15. PMID: 25891818.
      View in: PubMed
    55. Samanta D. Transient Kluver-Bucy syndrome from methamphetamine withdrawal. Neurol India. 2015 Mar-Apr; 63(2):267-8. PMID: 25948002.
      View in: PubMed
    56. 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
    57. 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
    58. Samanta D, Ramakrishnaiah R. Novel brain magnetic resonance imaging finding in a patient with trisomy 9p syndrome. Acta Neurol Belg. 2015 Sep; 115(3):431-2. PMID: 25527390.
      View in: PubMed
    59. 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
    60. Samanta D. Transient lesion in the splenium of the corpus callosum in status migrainosus. Acta Neurol Belg. 2015 Sep; 115(3):397-8. PMID: 25199654.
      View in: PubMed
    61. 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
    62. Samanta D. Reversible cerebral vasoconstriction syndrome: another health hazard of energy drinks? Clin Pediatr (Phila). 2015 Feb; 54(2):186-7. PMID: 25006115.
      View in: PubMed
    63. 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. PMID: 23576414.
      View in: PubMed
    64. 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. PMID: 19550057.
      View in: PubMed
    65. Krishnamurthy S, Samanta D, Yadav S. Trichuris dysentery syndrome with eosinophilic leukemoid reaction mimicking inflammatory bowel disease. J Postgrad Med. 2009 Jan-Mar; 55(1):76-7. PMID: 19242090.
      View in: PubMed
    66. Parakh A, Dubey AP, Samanta D. Caspofungin. Indian Pediatr. 2008 Nov; 45(11):905-10. PMID: 19029563.
      View in: PubMed
    67. Samanta D, Al Khalili Y. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. 2019 Dec 20. Electrical Status Epilepticus In Sleep (ESES).
    68. Samanta D, Lui F. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. 2019 Dec 2. Anti-NMDA Receptor Encephalitis.
    69. Humayun MJ, Samanta D, Carson RP. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. 2019 Dec 26. Clobazam.
    70. Riboldi GM, Samanta D, Frucht S. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. 2019 Dec 31. Ataxia Telangiectasia (Louis-Bar Syndrome).
    71. Kumar A, Samanta D, Arora R. Hemiplegic Migraine.
    72. Xixis KL, Samanta D, Keenaghan M. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. 2020 Jan 3. Febrile Seizure.
    73. Bokhari MR, Samanta D, Bokhari SRA. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-. 2019 Dec 31. Canavan Disease.
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