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Page 1
Intravenous immunoglobulin therapy in COVID-19-related encephalopathy.
J Neurol. 2021 Aug;268(8):2671-2675. doi: 10.1007/s00415-020-10248-0. Epub 2020 Oct 8.
J Neurol. 2021.
PMID: 33030607
Free PMC article.
The role of copy number variants in the genetic architecture of common familial epilepsies.
Epi4K Consortium.
Epi4K Consortium.
Epilepsia. 2024 Mar;65(3):792-804. doi: 10.1111/epi.17860. Epub 2024 Jan 20.
Epilepsia. 2024.
PMID: 38101940
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Individualised human phenotype ontology gene panels improve clinical whole exome and genome sequencing analytical efficacy in a cohort of developmental and epileptic encephalopathies.
Henry OJ, Stödberg T, Båtelson S, Rasi C, Stranneheim H, Wedell A.
Henry OJ, et al.
Mol Genet Genomic Med. 2023 Jul;11(7):e2167. doi: 10.1002/mgg3.2167. Epub 2023 Mar 26.
Mol Genet Genomic Med. 2023.
PMID: 36967109
Free PMC article.
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Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy.
Bennett MF, Hildebrand MS, Kayumi S, Corbett MA, Gupta S, Ye Z, Krivanek M, Burgess R, Henry OJ, Damiano JA, Boys A, Gécz J, Bahlo M, Scheffer IE, Berkovic SF.
Bennett MF, et al. Among authors: henry oj.
Neurol Genet. 2022 Jan 25;8(1):e652. doi: 10.1212/NXG.0000000000000652. eCollection 2022 Feb.
Neurol Genet. 2022.
PMID: 35097204
Free PMC article.
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