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2019 2
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2022 5
2023 6
2024 1

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Page 1
Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study.
Weiß C, Ziegler A, Becker LL, Johannsen J, Brennenstuhl H, Schreiber G, Flotats-Bastardas M, Stoltenburg C, Hartmann H, Illsinger S, Denecke J, Pechmann A, Müller-Felber W, Vill K, Blaschek A, Smitka M, van der Stam L, Weiss K, Winter B, Goldhahn K, Plecko B, Horber V, Bernert G, Husain RA, Rauscher C, Trollmann R, Garbade SF, Hahn A, von der Hagen M, Kaindl AM. Weiß C, et al. Among authors: becker ll. Lancet Child Adolesc Health. 2022 Jan;6(1):17-27. doi: 10.1016/S2352-4642(21)00287-X. Epub 2021 Oct 29. Lancet Child Adolesc Health. 2022. PMID: 34756190
Treatment of pediatric convulsive status epilepticus.
Becker LL, Gratopp A, Prager C, Elger CE, Kaindl AM. Becker LL, et al. Front Neurol. 2023 Jun 29;14:1175370. doi: 10.3389/fneur.2023.1175370. eCollection 2023. Front Neurol. 2023. PMID: 37456627 Free PMC article. Review.
Real-world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter study.
Kühne F, Becker LL, Bast T, Bertsche A, Borggraefe I, Boßelmann CM, Fahrbach J, Hertzberg C, Herz NA, Hirsch M, Holtkamp M, Janello C, Kluger GJ, Kurlemann G, Lerche H, Makridis KL, von Podewils F, Pringsheim M, Schubert-Bast S, Schulz J, Schulze-Bonhage A, Steinbart D, Steinhoff BJ, Strzelczyk A, Syrbe S, De Vries H, Wagner C, Wagner J, Wilken B, Prager C, Klotz KA, Kaindl AM. Kühne F, et al. Among authors: becker ll. Epilepsia Open. 2023 Jun;8(2):360-370. doi: 10.1002/epi4.12699. Epub 2023 Feb 6. Epilepsia Open. 2023. PMID: 36693811 Free PMC article.
Epilepsy surgery in early infancy: A retrospective, multicenter study.
Makridis KL, Klotz KA, Ramantani G, Becker LL, San Antonio-Arce V, Syrbe S, Wagner K, Shah MJ, Thomale UW, Tietze A, Elger CE, Borggraefe I, Kaindl AM. Makridis KL, et al. Among authors: becker ll. Epilepsia Open. 2023 Sep;8(3):1182-1189. doi: 10.1002/epi4.12791. Epub 2023 Jul 23. Epilepsia Open. 2023. PMID: 37458529 Free PMC article.
Monoallelic CRMP1 gene variants cause neurodevelopmental disorder.
Ravindran E, Arashiki N, Becker LL, Takizawa K, Lévy J, Rambaud T, Makridis KL, Goshima Y, Li N, Vreeburg M, Demeer B, Dickmanns A, Stegmann APA, Hu H, Nakamura F, Kaindl AM. Ravindran E, et al. Among authors: becker ll. Elife. 2022 Dec 13;11:e80793. doi: 10.7554/eLife.80793. Elife. 2022. PMID: 36511780 Free PMC article.
Proteome changes in autosomal recessive primary microcephaly.
Zaqout S, Mannaa A, Klein O, Krajewski A, Klose J, Luise-Becker L, Elsabagh A, Ferih K, Kraemer N, Ravindran E, Makridis K, Kaindl AM. Zaqout S, et al. Among authors: luise becker l. Ann Hum Genet. 2023 Mar;87(1-2):50-62. doi: 10.1111/ahg.12489. Epub 2022 Nov 29. Ann Hum Genet. 2023. PMID: 36448252
Immunofluorescence Staining of Paraffin Sections Step by Step.
Zaqout S, Becker LL, Kaindl AM. Zaqout S, et al. Among authors: becker ll. Front Neuroanat. 2020 Nov 9;14:582218. doi: 10.3389/fnana.2020.582218. eCollection 2020. Front Neuroanat. 2020. PMID: 33240048 Free PMC article.
18 results