Douglas Nordli to Mutation
This is a "connection" page, showing publications Douglas Nordli has written about Mutation.
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Clinical and Electroencephalographic Characteristics of Infantile-Onset Epilepsies Caused by Genetic Mutations. J Pediatr. 2017 05; 184:172-177.e1.
Score: 0.269
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Core Features Differentiate Dravet Syndrome from Febrile Seizures. J Pediatr. 2023 07; 258:113416.
Score: 0.103
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Cardiac phenotypic spectrum of KCNT1 mutations. Cardiol Young. 2020 Dec; 30(12):1935-1939.
Score: 0.086
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Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations. Ann Neurol. 2015 Apr; 77(4):675-83.
Score: 0.059
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Epileptic encephalopathies in infants and children. J Clin Neurophysiol. 2012 Oct; 29(5):420-4.
Score: 0.050
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Child Neurology: Dravet syndrome: when to suspect the diagnosis. Neurology. 2009 Sep 29; 73(13):e59-62.
Score: 0.040
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Severe peri-ictal respiratory dysfunction is common in Dravet syndrome. J Clin Invest. 2018 03 01; 128(3):1141-1153.
Score: 0.018