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Debopam Samanta

TitleAssistant 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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    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.
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    1. 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
    2. 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; PMCID: PMC4980965.
    3. 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
    4. 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
    5. 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
    6. 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
    7. 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
    8. 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
    9. 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
    10. 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
    11. 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
    12. Samanta D. Acneiform Lesion: Importance of Detailed Skin Examination. Indian J Pediatr. 2016 May; 83(5):485-6. PMID: 26558921.
      View in: PubMed
    13. 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
    14. 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
    15. 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
    16. 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
    17. 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
    18. 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
    19. 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; PMCID: PMC4611911.
    20. Samanta D. Possible Benign Partial Epilepsy. Indian Pediatr. 2015 Jul; 52(7):623. PMID: 26244962.
      View in: PubMed
    21. Samanta D. Horizontal Gaze Palsy: Additional Issues. Indian Pediatr. 2015 Jul; 52(7):624. PMID: 26244964.
      View in: PubMed
    22. 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
    23. 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
    24. Samanta D. Changing landscape of child neurology practice. Pediatr Neurol. 2015 Jun; 52(6):e15. PMID: 25891818.
      View in: PubMed
    25. Samanta D. Transient Kluver-Bucy syndrome from methamphetamine withdrawal. Neurol India. 2015 Mar-Apr; 63(2):267-8. PMID: 25948002.
      View in: PubMed
    26. 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
    27. 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
    28. 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
    29. 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
    30. 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
    31. 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
    32. 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
    33. 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
    34. Parakh A, Dubey AP, Samanta D. Caspofungin. Indian Pediatr. 2008 Nov; 45(11):905-10. PMID: 19029563.
      View in: PubMed
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