Connection
Debopam Samanta to Mutation
This is a "connection" page, showing publications Debopam Samanta has written about Mutation.
|
|
| |
Connection Strength |
|
 |
|
 |
| |
1.765 |
|
|
|
-
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: 0.462
-
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: 0.386
-
Samanta D. Chance Bias Arising from TSC2 Mutation Imbalance in the PREVeNT Trial. Ann Neurol. 2024 Feb; 95(2):413-414.
Score: 0.163
-
Samanta D. GRIN2A-related epilepsy and speech disorders: A comprehensive overview with a focus on the role of precision therapeutics. Epilepsy Res. 2023 01; 189:107065.
Score: 0.152
-
Samanta D, Ramakrishnaiah R, Frye RE. Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status. Neurol India. 2022 Sep-Oct; 70(5):2265-2267.
Score: 0.149
-
Samanta D. Reply to Cerebral Infarction in CARS2 Mutation. Pediatr Neurol. 2019 04; 93:66.
Score: 0.115
-
Samanta D, Gokden M. PEHO syndrome: KIF1A mutation and decreased activity of mitochondrial respiratory chain complex. J Clin Neurosci. 2019 Mar; 61:298-301.
Score: 0.114
-
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: 0.095
-
Samanta D. Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy. Neurol India. 2016 Mar-Apr; 64(2):327-8.
Score: 0.095
-
Binaafar S, Garshasbi M, Tavasoli AR, Badv RS, Hosseiny SMM, Samanta D, Rabbani B, Mahdieh N. Nonsyndromic Early-Onset Epileptic Encephalopathies: Two Novel KCTD7 Pathogenic Variants and a Literature Review. Dev Neurosci. 2021; 43(6):348-357.
Score: 0.035