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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 Sep;45(9):4373-4381. doi: 10.1007/s10072-024-07500-0. Epub 2024 Apr 12. Neurol Sci. 2024. PMID: 38607533 Free PMC article.
Fighting the Huntington's Disease with a G-Quadruplex-Forming Aptamer Specifically Binding to Mutant Huntingtin Protein: Biophysical Characterization, In Vitro and In Vivo Studies.
Riccardi C, D'Aria F, Digilio FA, Carillo MR, Amato J, Fasano D, De Rosa L, Paladino S, Melone MAB, Montesarchio D, Giancola C. Riccardi C, et al. Among authors: de rosa l. Int J Mol Sci. 2022 Apr 27;23(9):4804. doi: 10.3390/ijms23094804. Int J Mol Sci. 2022. PMID: 35563194 Free PMC article.
Posterior cerebral circulation in children with sickle cell anemia: an uncharted territory.
Salimbeni AF, De Rosa L, Volpato A, Viaro F, Pieroni A, Mozzetta S, Favruzzo F, Pes A, Zaccagnino M, Reggiani G, Boaro MP, Colombatti R, Manara R, Baracchini C. Salimbeni AF, et al. Among authors: de rosa l. Haematologica. 2024 Oct 24. doi: 10.3324/haematol.2024.285773. Online ahead of print. Haematologica. 2024. PMID: 39445409 Free article.
206 results