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Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: further delineation of a cobblestone-like phenotype.
Quattrocchi CC, Zanni G, Napolitano A, Longo D, Cordelli DM, Barresi S, Randisi F, Valente EM, Verdolotti T, Genovese E, Specchio N, Vitiello G, Spiegel R, Bertini E, Bernardi B. Quattrocchi CC, et al. Among authors: randisi f. Neurogenetics. 2013 Feb;14(1):77-83. doi: 10.1007/s10048-012-0352-7. Epub 2012 Dec 30. Neurogenetics. 2013. PMID: 23274687
Immunodeficiency in Vici syndrome: a heterogeneous phenotype.
Finocchi A, Angelino G, Cantarutti N, Corbari M, Bevivino E, Cascioli S, Randisi F, Bertini E, Dionisi-Vici C. Finocchi A, et al. Among authors: randisi f. Am J Med Genet A. 2012 Feb;158A(2):434-9. doi: 10.1002/ajmg.a.34244. Epub 2011 Sep 30. Am J Med Genet A. 2012. PMID: 21965116
Congenital Malformations of the Eye: A Pictorial Review and Clinico-Radiological Correlations.
Guarnera A, Valente P, Pasquini L, Moltoni G, Randisi F, Carducci C, Carboni A, Lucignani G, Napolitano A, Romanzo A, Longo D, Gandolfo C, Rossi-Espagnet MC. Guarnera A, et al. Among authors: randisi f. J Ophthalmol. 2024 Jan 30;2024:5993083. doi: 10.1155/2024/5993083. eCollection 2024. J Ophthalmol. 2024. PMID: 38322500 Free PMC article. Review.
22 results