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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 Feb 18; 107837. PMID: 33610461.
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Samanta D, Ramakrishnaiah R. Intravenous Immunoglobulin in the Treatment of Alternating Hemiplegia of Childhood. Clin Neuropharmacol. 2021 Jan-Feb 01; 44(1):23-26. PMID: 33177352.
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Samanta D. Recent Advances in the Diagnosis and Treatment of Neonatal Seizures. Neuropediatrics. 2020 Dec 08. PMID: 33291160.
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Samanta D. Management of Lennox-Gastaut syndrome beyond childhood: A comprehensive review. Epilepsy Behav. 2021 Jan; 114(Pt A):107612. PMID: 33243685.
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Samanta D, Ramakrishnaiah R. Early-Onset Parkinsonism and Halo Sign: Beta-propeller Proteinassociated Neurodegeneration. J Pediatr Neurosci. 2020 Jul-Sep; 15(3):325-327. PMID: 33531960.
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Samanta D, Cobb S. Freiberg's Infarction as the First Clinical Presentation of Sneddon Syndrome. J Pediatr Neurosci. 2020 Jul-Sep; 15(3):290-293. PMID: 33531949.
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Samanta D. Improving Management of Infantile Spasms by Adopting Implementation Science. Neuropediatrics. 2020 12; 51(6):377-388. PMID: 33049784.
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Samanta D. Epilepsy in Angelman syndrome: A scoping review. Brain Dev. 2021 Jan; 43(1):32-44. PMID: 32893075.
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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. PMID: 32853454.
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Samanta D. An Updated Review of Tuberous Sclerosis Complex-Associated Autism Spectrum Disorder. Pediatr Neurol. 2020 08; 109:4-11. PMID: 32563542.
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Lewis H, Samanta D, Örsell 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, Fernández-Jaén 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. PMID: 32446642.
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Samanta D, Arya K. Electroclinical Findings of SYNJ1 Epileptic Encephalopathy. J Pediatr Neurosci. 2020 Jan-Mar; 15(1):29-33. PMID: 32435303.
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Samanta D, Garrity L, Arya R. Refractory and Super-refractory Status Epilepticus. Indian Pediatr. 2020 03 15; 57(3):239-253. PMID: 32198865.
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Samanta D. Changing Landscape of Dravet Syndrome Management: An Overview. Neuropediatrics. 2020 04; 51(2):135-145. PMID: 32079034.
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Samanta D. E-Cigarettes and Seizures. Pediatr Neurol. 2020 04; 105:75. PMID: 32029335.
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Samanta D. Ketamine Infusion for Super Refractory Status Epilepticus in Alternating Hemiplegia of Childhood. Neuropediatrics. 2020 06; 51(3):225-228. PMID: 32016945.
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Samanta D. Levetiracetam is Still Not a First-line Treatment in Neonatal Seizures. Indian Pediatr. 2020 01 15; 57(1):80. PMID: 31937712.
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Samanta D. Rhizomelic chondrodysplasia punctata: Role of EEG as a biomarker of impending epilepsy. eNeurologicalSci. 2020 Mar; 18:100218. PMID: 31853509.
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Samanta D. PCDH19-Related Epilepsy Syndrome: A Comprehensive Clinical Review. Pediatr Neurol. 2020 04; 105:3-9. PMID: 32057594.
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Samanta D. Ketamine in Refractory Neonatal Seizures. Pediatr Neurol. 2020 05; 106:76. PMID: 31917102.
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Samanta D. Management of Alternating Hemiplegia of Childhood: A Review. Pediatr Neurol. 2020 02; 103:12-20. PMID: 31836335.
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Harada Y, Ramakrishnaiah R, Arya K, Samanta D. Extensive reversible myelopathy secondary to acute quadriventricular noncommunicating hydrocephalus. Childs Nerv Syst. 2019 11; 35(11):2023-2026. PMID: 31375904.
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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. PMID: 31292937.
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Samanta D, Cobb S, Arya K. Sneddon Syndrome: A Comprehensive Overview. J Stroke Cerebrovasc Dis. 2019 Aug; 28(8):2098-2108. PMID: 31160219.
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Samanta D, Ramakrishnaiah R. Recurrent Oral Ulcers in a Child With Seizures. Pediatr Neurol. 2020 02; 103:89-90. PMID: 31122835.
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Samanta D. Cannabidiol: A Review of Clinical Efficacy and Safety in Epilepsy. Pediatr Neurol. 2019 07; 96:24-29. PMID: 31053391.
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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. PMID: 30879264.
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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.
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Samanta D, Zarate YA. Widening phenotypic spectrum of GABBR2 mutation. Acta Neurol Belg. 2019 Sep; 119(3):493-496. PMID: 30707408.
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Samanta D. A Girl with Palpitations and Periodic Weakness. Indian J Pediatr. 2019 05; 86(5):480. PMID: 30656561.
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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.
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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.
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Samanta D. Reply to Cerebral Infarction in CARS2 Mutation. Pediatr Neurol. 2019 04; 93:66. PMID: 30686629.
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Samanta D. Headaches in Loyes-Dietz Syndrome. J Child Neurol. 2018 Dec 19; 883073818815039. PMID: 30565496.
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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.
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Malatesta LM, Samanta D, Ramakrishnaiah R. An Unusual Cause of Recurrent Facial Nerve Palsy. Pediatr Neurol. 2019 02; 91:68-69. PMID: 30471898.
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Samanta D. Effects of Separation on Children's Neurodevelopment. Pediatr Neurol. 2019 02; 91:72. PMID: 30471897.
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Samanta D, Alvarez-Nunez F. Mass-Like Lesion on Brain Magnetic Resonance Imaging. Pediatr Neurol. 2018 12; 89:71-72. PMID: 30396829.
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Gabriel GK, Samanta D, Cobb S. An Unusual Holohemispheric Abnormality. Pediatr Neurol. 2019 01; 90:74-75. PMID: 30420108.
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Samanta D. Asymmetric photic driving response: importance of reviewing the video. Acta Neurol Belg. 2020 Apr; 120(2):395-397. PMID: 30173312.
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Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76. PMID: 30327240.
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Samanta D, Gokden M, Willis E. Clinicopathologic Findings of CARS2 Mutation. Pediatr Neurol. 2018 10; 87:65-69. PMID: 30139652.
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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. PMID: 29808309.
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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.
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Samanta D, Willis E. KIAA2022-related disorders can cause Jeavons (eyelid myoclonia with absence) syndrome. Acta Neurol Belg. 2020 Feb; 120(1):205-207. PMID: 29417424.
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Willis E, Samanta D, Kanfi A. A Not Uncommon Cause of Stroke Mimicker in Children. Pediatr Neurol. 2018 03; 80:92-93. PMID: 29229230.
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Samanta D. Surendra Nath Sehgal: A pioneer in rapamycin discovery. Indian J Cancer. 2017 Oct-Dec; 54(4):697-698. PMID: 30082562.
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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.
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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.
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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.
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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.
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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.
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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.
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Samanta D. Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy. Neurol India. 2016 Mar-Apr; 64(2):327-8. PMID: 26954813.
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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.
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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.
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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.
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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.
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Samanta D. Acneiform Lesion: Importance of Detailed Skin Examination. Indian J Pediatr. 2016 May; 83(5):485-6. PMID: 26558921.
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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.
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Samanta D. Osteomyelitis of bilateral great toes: iatrogenic complication of nerve conduction study. Acta Neurol Belg. 2016 Sep; 116(3):429-30. PMID: 26498128.
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Samanta D. Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome. Acta Neurol Belg. 2016 Sep; 116(3):363-4. PMID: 26476657.
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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.
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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.
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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.
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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.
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Samanta D. Possible Benign Partial Epilepsy. Indian Pediatr. 2015 Jul; 52(7):623. PMID: 26244962.
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Samanta D. Horizontal Gaze Palsy: Additional Issues. Indian Pediatr. 2015 Jul; 52(7):624. PMID: 26244964.
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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.
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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.
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Samanta D. Changing landscape of child neurology practice. Pediatr Neurol. 2015 Jun; 52(6):e15. PMID: 25891818.
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Samanta D. Transient Kluver-Bucy syndrome from methamphetamine withdrawal. Neurol India. 2015 Mar-Apr; 63(2):267-8. PMID: 25948002.
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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.
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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.
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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.
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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.
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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.
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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.
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Samanta D. Reversible cerebral vasoconstriction syndrome: another health hazard of energy drinks? Clin Pediatr (Phila). 2015 Feb; 54(2):186-7. PMID: 25006115.
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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.
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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.
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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.
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Parakh A, Dubey AP, Samanta D. Caspofungin. Indian Pediatr. 2008 Nov; 45(11):905-10. PMID: 19029563.
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Samanta D, Al Khalili Y. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.
2019 Dec 20. Electrical Status Epilepticus In Sleep (ESES).
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Samanta D, Lui F. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.
2019 Dec 2. Anti-NMDA Receptor Encephalitis.
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Humayun MJ, Samanta D, Carson RP. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.
2019 Dec 26. Clobazam.
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Riboldi GM, Samanta D, Frucht S. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.
2019 Dec 31. Ataxia Telangiectasia (Louis-Bar Syndrome).
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Kumar A, Samanta D, Arora R. Hemiplegic Migraine.
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Xixis KL, Samanta D, Keenaghan M. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.
2020 Jan 3. Febrile Seizure.
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Bokhari MR, Samanta D, Bokhari SRA. StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.
2019 Dec 31. Canavan Disease.