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																		 Connection
 
																		 Debopam Samanta to Male  
																		
																	 
																		This is a "connection" page, showing publications Debopam Samanta has written about Male.   
																		
																	 
																			
																					
	
						
				
		
			
			
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					|  | Connection Strength |  |  
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					|  | 0.957 |  |  |  |  
		
		
			
				Samanta D, Newell G, Caraway AR, Brock E, Albert GW, Novotny EJ, Depositario Cabacar DF, Oluigbo CO, Gaillard WD, Tatachar P, Bolton JB, Wong-Kisiel L, Romanowski EF, Mcnamara NA, Eschbach K, Alexander AL, Auguste KI, Gonzalez-Giraldo E, Bernardo D, Ostendorf AP, Coryell J, Karia S, Karakas C, Javarayee PK, Pichon PD, Olaya J, Shrey DW, Reddy SB, Ganesh A, Hauptman JS, Singh RK, Ciliberto M, Marashly A, Grinspan ZM, Nangia S, Arredondo K, Miller DJ, Sattar S, Montenegro M, Agarwal N, Galan FN, Wagner J, Abel TJ, Knox AT, Perry MS. Factors Associated With More Medication Trials Before Surgical Evaluation and Postsurgical Outcomes in Pediatric Drug-Resistant Epilepsy. Neurology. 2025 Nov 11; 105(9):e214198.	
				
				
					Score: 0.059
				
				Samanta D, Ramakrishnaiah R. Intravenous Immunoglobulin in the Treatment of Alternating Hemiplegia of Childhood. Clin Neuropharmacol. 2021 Jan-Feb 01; 44(1):23-26.	
				
				
					Score: 0.043
				
				Samanta D. Epilepsy in Angelman syndrome: A scoping review. Brain Dev. 2021 Jan; 43(1):32-44.	
				
				
					Score: 0.042
				
				Samanta D. Ketamine Infusion for Super Refractory Status Epilepticus in Alternating Hemiplegia of Childhood. Neuropediatrics. 2020 06; 51(3):225-228.	
				
				
					Score: 0.040
				
				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.	
				
				
					Score: 0.038
				
				Samanta D, Zarate YA. Widening phenotypic spectrum of GABBR2 mutation. Acta Neurol Belg. 2019 Sep; 119(3):493-496.	
				
				
					Score: 0.037
				
				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.	
				
				
					Score: 0.037
				
				Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76.	
				
				
					Score: 0.036
				
				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.	
				
				
					Score: 0.031
				
				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.	
				
				
					Score: 0.031
				
				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.	
				
				
					Score: 0.031
				
				Samanta D. A 15-year-old with seizures: late diagnosis of pyridoxine-dependent epilepsy. Acta Neurol Belg. 2016 Dec; 116(4):667-669.	
				
				
					Score: 0.031
				
				Samanta D. Sporadic hemiplegic migraine and giant tumefactive perivascular space: Is there an association? Acta Neurol Belg. 2016 Dec; 116(4):619-620.	
				
				
					Score: 0.030
				
				Samanta D. Influenza B-associated acute necrotizing encephalopathy of childhood: a report from North America. Acta Neurol Belg. 2016 Sep; 116(3):383-5.	
				
				
					Score: 0.030
				
				Samanta D. Acneiform Lesion: Importance of Detailed Skin Examination. Indian J Pediatr. 2016 May; 83(5):485-6.	
				
				
					Score: 0.030
				
				Samanta D. Osteomyelitis of bilateral great toes: iatrogenic complication of nerve conduction study. Acta Neurol Belg. 2016 Sep; 116(3):429-30.	
				
				
					Score: 0.030
				
				Samanta D. Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome. Acta Neurol Belg. 2016 Sep; 116(3):363-4.	
				
				
					Score: 0.030
				
				Samanta D. Possible Benign Partial Epilepsy. Indian Pediatr. 2015 Jul; 52(7):623.	
				
				
					Score: 0.029
				
				Samanta D. Horizontal Gaze Palsy: Additional Issues. Indian Pediatr. 2015 Jul; 52(7):624.	
				
				
					Score: 0.029
				
				Samanta D, Ramakrishnaiah R. De novo R853Q mutation of SCN2A gene and West syndrome. Acta Neurol Belg. 2015 Dec; 115(4):773-6.	
				
				
					Score: 0.029
				
				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.	
				
				
					Score: 0.028
				
				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.	
				
				
					Score: 0.028
				
				Samanta D. Transient lesion in the splenium of the corpus callosum in status migrainosus. Acta Neurol Belg. 2015 Sep; 115(3):397-8.	
				
				
					Score: 0.028
				
				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.	
				
				
					Score: 0.027
				
				Samanta D. Reversible cerebral vasoconstriction syndrome: another health hazard of energy drinks? Clin Pediatr (Phila). 2015 Feb; 54(2):186-7.	
				
				
					Score: 0.027
				
				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.	
				
				
					Score: 0.015
				
				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.	
				
				
					Score: 0.014
				
				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.	
				
				
					Score: 0.014
				
				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.	
				
				
					Score: 0.013
				
				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.	
				
				
					Score: 0.011
				
				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.	
				
				
					Score: 0.010
				
				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.	
				
				
					Score: 0.010
				
				Malatesta LM, Samanta D, Ramakrishnaiah R. An Unusual Cause of Recurrent Facial Nerve Palsy. Pediatr Neurol. 2019 02; 91:68-69.	
				
				
					Score: 0.009
				
				Gabriel GK, Samanta D, Cobb S. An Unusual Holohemispheric Abnormality. Pediatr Neurol. 2019 01; 90:74-75.	
				
				
					Score: 0.009
				
				Willis E, Samanta D, Kanfi A. A Not Uncommon Cause of Stroke Mimicker in Children. Pediatr Neurol. 2018 03; 80:92-93.	
				
				
					Score: 0.009
				
				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.	
				
				
					Score: 0.006
				
				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.	
				
				
					Score: 0.005
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																					              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.
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