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Developmental haemostasis. Impact for clinical haemostasis laboratories.
Monagle P, Barnes C, Ignjatovic V, Furmedge J, Newall F, Chan A, De Rosa L, Hamilton S, Ragg P, Robinson S, Auldist A, Crock C, Roy N, Rowlands S. Monagle P, et al. Among authors: de rosa l. Thromb Haemost. 2006 Feb;95(2):362-72. doi: 10.1160/TH05-01-0047. Thromb Haemost. 2006. PMID: 16493500
Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family.
Trinchillo A, Valente V, Esposito M, Migliaccio M, Iovino A, Picciocchi M, Cuomo N, Caccavale C, Nocerino C, De Rosa L, Salvatore E, Pierantoni GM, Menchise V, Paladino S, Criscuolo C. Trinchillo A, et al. Among authors: de rosa l. Neurol Sci. 2024 Apr 12. doi: 10.1007/s10072-024-07500-0. Online ahead of print. Neurol Sci. 2024. PMID: 38607533
Allele-specific CRISPR-Cas9 editing of dominant epidermolysis bullosa simplex in human epidermal stem cells.
Cattaneo C, Enzo E, De Rosa L, Sercia L, Consiglio F, Forcato M, Bicciato S, Paiardini A, Basso G, Tagliafico E, Paganelli A, Fiorentini C, Magnoni C, Latella MC, De Luca M. Cattaneo C, et al. Among authors: de rosa l. Mol Ther. 2024 Feb 7;32(2):372-383. doi: 10.1016/j.ymthe.2023.11.027. Epub 2023 Dec 5. Mol Ther. 2024. PMID: 38053334 Free article.
188 results