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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.
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
Nuck cyst: a rare cause of inguinal swelling in infancy.
Papparella A, Vaccaro S, Accardo M, DE Rosa L, Ronchi A, Noviello C. Papparella A, et al. Among authors: de rosa l. Minerva Pediatr (Torino). 2021 Apr;73(2):180-183. doi: 10.23736/S2724-5276.18.05205-2. Epub 2018 Jul 23. Minerva Pediatr (Torino). 2021. PMID: 30035501
191 results