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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: menchise 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.
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.
TRPV4 mutations in children with congenital distal spinal muscular atrophy.
Fiorillo C, Moro F, Brisca G, Astrea G, Nesti C, Bálint Z, Olschewski A, Meschini MC, Guelly C, Auer-Grumbach M, Battini R, Pedemonte M, Romano A, Menchise V, Biancheri R, Santorelli FM, Bruno C. Fiorillo C, et al. Among authors: menchise v. Neurogenetics. 2012 Aug;13(3):195-203. doi: 10.1007/s10048-012-0328-7. Epub 2012 Apr 25. Neurogenetics. 2012. PMID: 22526352
Novel Gd(III)-based probes for MR molecular imaging of matrix metalloproteinases.
Gringeri CV, Menchise V, Rizzitelli S, Cittadino E, Catanzaro V, Dati G, Chaabane L, Digilio G, Aime S. Gringeri CV, et al. Among authors: menchise v. Contrast Media Mol Imaging. 2012 Mar-Apr;7(2):175-84. doi: 10.1002/cmmi.478. Contrast Media Mol Imaging. 2012. PMID: 22434630 Free article.
35 results