Chilcott E - Search Results

1

Hereditary spastic paraplegia: Novel insights into the pathogenesis and management.

Awuah WA, Tan JK, Shkodina AD, Ferreira T, Adebusoye FT, Mazzoleni A, Wellington J, David L, Chilcott E, Huang H, Abdul-Rahman T, Shet V, Atallah O, Kalmanovich J, Jiffry R, Madhu DE, Sikora K, Kmyta O, Delva MY. Awuah WA, et al. Among authors: chilcott e. SAGE Open Med. 2023 Dec 29;12:20503121231221941. doi: 10.1177/20503121231221941. eCollection 2024. SAGE Open Med. 2023. PMID: 38162912 Free PMC article. Review.

2

AAV9-mediated SMN gene therapy rescues cardiac desmin but not lamin A/C and elastin dysregulation in Smn2B/- spinal muscular atrophy mice.

Brown SJ, Šoltić D, Synowsky SA, Shirran SL, Chilcott E, Shorrock HK, Gillingwater TH, Yáñez-Muñoz RJ, Schneider B, Bowerman M, Fuller HR. Brown SJ, et al. Among authors: chilcott e. Hum Mol Genet. 2023 Oct 4;32(20):2950-2965. doi: 10.1093/hmg/ddad121. Hum Mol Genet. 2023. PMID: 37498175 Free PMC article.

3

Enhanced expression of the human Survival motor neuron 1 gene from a codon-optimised cDNA transgene in vitro and in vivo.

Nafchi NAM, Chilcott EM, Brown S, Fuller HR, Bowerman M, Yáñez-Muñoz RJ. Nafchi NAM, et al. Among authors: chilcott em. Gene Ther. 2023 Dec;30(12):812-825. doi: 10.1038/s41434-023-00406-0. Epub 2023 Jun 15. Gene Ther. 2023. PMID: 37322133

4

Correction: Systematic review and meta-analysis determining the benefits of in vivo genetic therapy in spinal muscular atrophy rodent models.

Chilcott EM, Muiruri EW, Hirst TC, Yáñez-Muñoz RJ. Chilcott EM, et al. Gene Ther. 2023 Feb;30(1-2):188. doi: 10.1038/s41434-022-00377-8. Gene Ther. 2023. PMID: 36437357 Free PMC article. No abstract available.

5

Exploring seizure management in hospitals, unmet need, and the impact of the COVID-19 pandemic on seizure presentations to hospital.

Ellis B, Chilcott E, John K, Parry J, Capeling L, Lawthom C, Harding K, Anderson J. Ellis B, et al. Among authors: chilcott e. Seizure. 2022 Nov;102:51-53. doi: 10.1016/j.seizure.2022.09.014. Epub 2022 Sep 22. Seizure. 2022. PMID: 36191475 Free PMC article.

6

Genetic therapeutic advancements for Dravet Syndrome.

Chilcott E, Díaz JA, Bertram C, Berti M, Karda R. Chilcott E, et al. Epilepsy Behav. 2022 Jul;132:108741. doi: 10.1016/j.yebeh.2022.108741. Epub 2022 May 30. Epilepsy Behav. 2022. PMID: 35653814 Free article. Review.

7

Systematic review and meta-analysis determining the benefits of in vivo genetic therapy in spinal muscular atrophy rodent models.

Chilcott EM, Muiruri EW, Hirst TC, Yáñez-Muñoz RJ. Chilcott EM, et al. Gene Ther. 2022 Sep;29(9):498-512. doi: 10.1038/s41434-021-00292-4. Epub 2021 Oct 6. Gene Ther. 2022. PMID: 34611322 Free PMC article.

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