 Connection
Connection
 
																	
																		
Debopam Samanta to Brain  
																	
																		
																	
																	
																		This is a "connection" page, showing publications Debopam Samanta has written about Brain.  
 
																	
																		
																	
																	
																			
																					
	
						
				
		
			
			
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					|  | 2.124 |  |  |  | 
			
		 
	 	
	
	
		
		
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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.	
				
				
					Score: 0.342
				 
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				Samanta D, Alvarez-Nunez F. Mass-Like Lesion on Brain Magnetic Resonance Imaging. Pediatr Neurol. 2018 12; 89:71-72.	
				
				
					Score: 0.335
				 
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				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: 0.283
				 
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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.	
				
				
					Score: 0.278
				 
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				Samanta D. Acneiform Lesion: Importance of Detailed Skin Examination. Indian J Pediatr. 2016 May; 83(5):485-6.	
				
				
					Score: 0.275
				 
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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.	
				
				
					Score: 0.259
				 
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				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.	
				
				
					Score: 0.128
				 
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				Gabriel GK, Samanta D, Cobb S. An Unusual Holohemispheric Abnormality. Pediatr Neurol. 2019 01; 90:74-75.	
				
				
					Score: 0.084
				 
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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.	
				
				
					Score: 0.071
				 
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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.	
				
				
					Score: 0.068