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Cerliponase Alfa for the Treatment of Atypical Phenotypes of CLN2 Disease: A Retrospective Case Series.
Wibbeler E, Wang R, Reyes EL, Specchio N, Gissen P, Guelbert N, Nickel M, Schwering C, Lehwald L, Trivisano M, Lee L, Amato G, Cohen-Pfeffer J, Shediac R, Leal-Pardinas F, Schulz A. Wibbeler E, et al. Among authors: lee l. J Child Neurol. 2021 May;36(6):468-474. doi: 10.1177/0883073820977997. Epub 2020 Dec 23. J Child Neurol. 2021. PMID: 33356800 Free PMC article.
Investigating health-related quality of life in rare diseases: a case study in utility value determination for patients with CLN2 disease (neuronal ceroid lipofuscinosis type 2).
Gissen P, Specchio N, Olaye A, Jain M, Butt T, Ghosh W, Ruban-Fell B, Griffiths A, Camp C, Sisic Z, Schwering C, Wibbeler E, Trivisano M, Lee L, Nickel M, Mortensen A, Schulz A. Gissen P, et al. Among authors: lee l. Orphanet J Rare Dis. 2021 May 12;16(1):217. doi: 10.1186/s13023-021-01829-x. Orphanet J Rare Dis. 2021. PMID: 33980287 Free PMC article.
Taboo language across the globe: A multi-lab study.
Sulpizio S, Günther F, Badan L, Basclain B, Brysbaert M, Chan YL, Ciaccio LA, Dudschig C, Duñabeitia JA, Fasoli F, Ferrand L, Filipović Đurđević D, Guerra E, Hollis G, Job R, Jornkokgoud K, Kahraman H, Kgolo-Lotshwao N, Kinoshita S, Kos J, Lee L, Lee NH, Mackenzie IG, Manojlović M, Manouilidou C, Martinic M, Del Carmen Méndez M, Mišić K, Chiangmai NN, Nikolaev A, Oganyan M, Rusconi P, Samo G, Tse CS, Westbury C, Wongupparaj P, Yap MJ, Marelli M. Sulpizio S, et al. Among authors: lee l. Behav Res Methods. 2024 May 9. doi: 10.3758/s13428-024-02376-6. Online ahead of print. Behav Res Methods. 2024. PMID: 38724878
9,984 results