Connection
Virginia Willis to Electroencephalography
This is a "connection" page, showing publications Virginia Willis has written about Electroencephalography.
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0.301 |
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Samanta D, Gokden M, Willis E. Clinicopathologic Findings of CARS2 Mutation. Pediatr Neurol. 2018 10; 87:65-69.
Score: 0.139
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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.
Score: 0.109
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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.
Score: 0.027
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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: 0.026