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Visual impairment in FOXG1-mutated individuals and mice.
Boggio EM, Pancrazi L, Gennaro M, Lo Rizzo C, Mari F, Meloni I, Ariani F, Panighini A, Novelli E, Biagioni M, Strettoi E, Hayek J, Rufa A, Pizzorusso T, Renieri A, Costa M. Boggio EM, et al. Among authors: hayek j. Neuroscience. 2016 Jun 2;324:496-508. doi: 10.1016/j.neuroscience.2016.03.027. Epub 2016 Mar 19. Neuroscience. 2016. PMID: 27001178 Free article.
Private inherited microdeletion/microduplications: implications in clinical practice.
Mencarelli MA, Katzaki E, Papa FT, Sampieri K, Caselli R, Uliana V, Pollazzon M, Canitano R, Mostardini R, Grosso S, Longo I, Ariani F, Meloni I, Hayek J, Balestri P, Mari F, Renieri A. Mencarelli MA, et al. Among authors: hayek j. Eur J Med Genet. 2008 Sep-Oct;51(5):409-16. doi: 10.1016/j.ejmg.2008.06.003. Epub 2008 Jul 9. Eur J Med Genet. 2008. PMID: 18657637
NLRP3 inflammasome-mitochondrion loop in autism spectrum disorder.
Vallese A, Cordone V, Ferrara F, Guiotto A, Gemmo L, Cervellati F, Hayek J, Pecorelli A, Valacchi G. Vallese A, et al. Among authors: hayek j. Free Radic Biol Med. 2024 Nov 20;225:581-594. doi: 10.1016/j.freeradbiomed.2024.10.297. Epub 2024 Oct 19. Free Radic Biol Med. 2024. PMID: 39433111
187 results