Connection
Virginia Willis to Child
This is a "connection" page, showing publications Virginia Willis has written about Child.
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0.250 |
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Samanta D, Willis E. KIAA2022-related disorders can cause Jeavons (eyelid myoclonia with absence) syndrome. Acta Neurol Belg. 2020 Feb; 120(1):205-207.
Score: 0.064
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Samanta D, Willis E. Focal seizure associated with human parvovirus B19 infection in a non-encephalopathic child. World J Pediatr. 2016 Feb; 12(1):118-20.
Score: 0.055
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Sharp GB, Samanta D, Willis E. Options for pharmacoresistant epilepsy in children: when medications don't work. Pediatr Ann. 2015 Feb; 44(2):e43-8.
Score: 0.052
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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: 0.052
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Bradley L, Bahgat D, Sharp G, Willis E, Ocal E, Albert G, Serletis D. Disconnective Hemispherotomy for Medically Intractable Status Epilepticus in an 8-Year-Old Child. J Ark Med Soc. 2015 Oct; 112(6):86-7.
Score: 0.014
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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: 0.013