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A novel mutation in GCH-1 gene in a case of dopa-responsive dystonia.
De Rosa A, Carducci C, Antonozzi I, Giovanniello T, Xhoxhi E, Criscuolo C, Menchise V, Striano S, Filla A, De Michele G. De Rosa A, et al. Among authors: menchise v. J Neurol. 2007 Aug;254(8):1133-4. doi: 10.1007/s00415-006-0475-6. Epub 2007 Apr 6. J Neurol. 2007. PMID: 17410324 No abstract available.
Very late onset in ataxia oculomotor apraxia type I.
Criscuolo C, Mancini P, Menchise V, Saccà F, De Michele G, Banfi S, Filla A. Criscuolo C, et al. Among authors: menchise v. Ann Neurol. 2005 May;57(5):777. doi: 10.1002/ana.20463. Ann Neurol. 2005. PMID: 15852392 Free article. No abstract available.
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: menchise v. Neurol Sci. 2024 Apr 12. doi: 10.1007/s10072-024-07500-0. Online ahead of print. Neurol Sci. 2024. PMID: 38607533
Sonosensitive theranostic liposomes for preclinical in vivo MRI-guided visualization of doxorubicin release stimulated by pulsed low intensity non-focused ultrasound.
Rizzitelli S, Giustetto P, Cutrin JC, Delli Castelli D, Boffa C, Ruzza M, Menchise V, Molinari F, Aime S, Terreno E. Rizzitelli S, et al. Among authors: menchise v. J Control Release. 2015 Mar 28;202:21-30. doi: 10.1016/j.jconrel.2015.01.028. Epub 2015 Jan 24. J Control Release. 2015. PMID: 25626083 Free article.
35 results