CrossRef Text and Data Mining
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Clinical Features and Treatment Efficacy in CDKL5 Mutation-Related Epileptic Encephalopathy in the Infant
Chung Mo Koo, Se Hee Kim, Heung Dong Kim, Joon Soo Lee, Jong Rak Choi, Seung-Tae Lee, Hoon-Chul Kang
Ann Child Neurol. 2019;27(2):33-37.   Published online June 3, 2019
DOI: https://doi.org/10.26815/acn.2019.00052

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Clinical Features and Treatment Efficacy in CDKL5 Mutation-Related Epileptic Encephalopathy in the Infant
Annals of Child Neurology. 2019;27(2):33-37   Crossref logo
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CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life
Developmental Medicine & Child Neurology. 2011;53(4):354-360   Crossref logo
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Clinical features of early myoclonic encephalopathy caused by a CDKL5 mutation
Brain and Development. 2019;   Crossref logo
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CDKL5 gene-related epileptic encephalopathy: electroclinical findings in the first year of life
Developmental Medicine & Child Neurology. 2011;53(4):296-297   Crossref logo
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PCDH19-related infantile epileptic encephalopathy: An unusual X-linked inheritance disorder
Human Mutation. 2012;33(4):627-634   Crossref logo
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Myoclonic encephalopathy in the CDKL5 gene mutation
Clinical Neurophysiology. 2006;117(1):223-227   Crossref logo
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Historic, Clinical, and Prognostic Features of Epileptic Encephalopathies Caused by CDKL5 Mutations
Pediatric Neurology. 2012;46(2):101-105   Crossref logo
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Recurrent occurrences of CDKL5 mutations in patients with epileptic encephalopathy
Human Genome Variation. 2015;2(1):   Crossref logo
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CDKL5 variant in a boy with Infantile Epileptic Encephalopathy: Case report
Brain and Development. 2015;37(4):446-448   Crossref logo
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Molecular and genetic insights into an infantile epileptic encephalopathy – CDKL5 disorder
Frontiers in Biology. 2017;12(1):1-6   Crossref logo
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