 Connection
Debopam Samanta to Infant
This is a "connection" page, showing publications Debopam Samanta has written about Infant.
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Connection Strength |
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1.255 |
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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.
Score: 0.104
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Samanta D. Improving Management of Infantile Spasms by Adopting Implementation Science. Neuropediatrics. 2020 12; 51(6):377-388.
Score: 0.103
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Samanta D. Epilepsy in Angelman syndrome: A scoping review. Brain Dev. 2021 Jan; 43(1):32-44.
Score: 0.102
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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.
Score: 0.090
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Samanta D. Asymmetric photic driving response: importance of reviewing the video. Acta Neurol Belg. 2020 Apr; 120(2):395-397.
Score: 0.089
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Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76.
Score: 0.088
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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.
Score: 0.087
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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: 0.076
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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.
Score: 0.075
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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: 0.075
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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.
Score: 0.074
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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.
Score: 0.072
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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.
Score: 0.070
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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.
Score: 0.067
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Buijsse N, Jansen FE, Ockeloen CW, van Kempen MJA, Zeidler S, Willemsen MH, Scarano E, Monticone S, Zonneveld-Huijssoon E, Low KJ, Bayat A, Sisodiya SM, Samanta D, Lesca G, de Jong D, Giltay JC, Verbeek NE, Kleefstra T, Brilstra EH, Vlaskamp DRM. Epilepsy is an important feature of KBG syndrome associated with poorer developmental outcome. Epilepsia Open. 2023 Dec; 8(4):1300-1313.
Score: 0.031
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Yuskaitis CJ, Mytinger JR, Baumer FM, Zhang B, Liu S, Samanta D, Hussain SA, Yozawitz EG, Keator CG, Joshi C, Singh RK, Bhatia S, Bhalla S, Shellhaas R, Harini C. Association of Time to Clinical Remission With Sustained Resolution in Children With New-Onset Infantile Spasms. Neurology. 2022 11 29; 99(22):e2494-e2503.
Score: 0.029
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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: 0.025
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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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