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Phloroglucinol-Derived Medications are Effective in Reducing Pain and Spasms of Urinary and Biliary Tracts: Results of Phase 3 Multicentre, Open-Label, Randomized, Comparative Studies of Clinical Effectiveness and Safety.
Corvino A, Magli E, Minale M, Autelitano A, Valente V, Pierantoni GM. Corvino A, et al. Among authors: valente v. Adv Ther. 2023 Feb;40(2):619-640. doi: 10.1007/s12325-022-02347-3. Epub 2022 Nov 29. Adv Ther. 2023. PMID: 36443585 Free PMC article.
Double knock-out of Hmga1 and Hipk2 genes causes perinatal death associated to respiratory distress and thyroid abnormalities in mice.
Gerlini R, Amendola E, Conte A, Valente V, Tornincasa M, Credendino SC, Cammarota F, Gentile C, Di Guida L, Paladino S, De Vita G, Fusco A, Pierantoni GM. Gerlini R, et al. Among authors: valente v. Cell Death Dis. 2019 Oct 3;10(10):747. doi: 10.1038/s41419-019-1975-5. Cell Death Dis. 2019. PMID: 31582725 Free PMC article.
Phenotypic Effects of Homeodomain-Interacting Protein Kinase 2 Deletion in Mice.
De Biase D, Valente V, Conte A, Cammarota F, Boccella N, D'Esposito L, d'Aquino I, Paciello O, Paladino S, Pierantoni GM. De Biase D, et al. Among authors: valente v. Int J Mol Sci. 2021 Aug 2;22(15):8294. doi: 10.3390/ijms22158294. Int J Mol Sci. 2021. PMID: 34361060 Free PMC article.
Down Syndrome Fetal Fibroblasts Display Alterations of Endosomal Trafficking Possibly due to SYNJ1 Overexpression.
De Rosa L, Fasano D, Zerillo L, Valente V, Izzo A, Mollo N, Amodio G, Polishchuk E, Polishchuk R, Melone MAB, Criscuolo C, Conti A, Nitsch L, Remondelli P, Pierantoni GM, Paladino S. De Rosa L, et al. Among authors: valente v. Front Genet. 2022 May 13;13:867989. doi: 10.3389/fgene.2022.867989. eCollection 2022. Front Genet. 2022. PMID: 35646085 Free PMC article.
Chronic exposure to l-BMAA cyanotoxin induces cytoplasmic TDP-43 accumulation and glial activation, reproducing an amyotrophic lateral sclerosis-like phenotype in mice.
Anzilotti S, Valente V, Brancaccio P, Franco C, Casamassa A, Lombardi G, Palazzi A, Conte A, Paladino S, Canzoniero LMT, Annunziato L, Pierantoni GM, Pignataro G. Anzilotti S, et al. Among authors: valente v. Biomed Pharmacother. 2023 Nov;167:115503. doi: 10.1016/j.biopha.2023.115503. Epub 2023 Sep 18. Biomed Pharmacother. 2023. PMID: 37729728 Free 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: valente v. 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.
254 results