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Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin-remodeling genes.
Provenzano A, La Barbera A, Scagnet M, Pagliazzi A, Traficante G, Pantaleo M, Tiberi L, Vergani D, Kurtas NE, Guarducci S, Bargiacchi S, Forzano G, Artuso R, Palazzo V, Kura A, Giordano F, di Feo D, Mortilla M, De Filippi C, Mattei G, Garavelli L, Giusti B, Genitori L, Zuffardi O, Giglio S. Provenzano A, et al. Among authors: giordano f. Hum Genet. 2021 Apr;140(4):625-647. doi: 10.1007/s00439-020-02231-6. Epub 2020 Dec 18. Hum Genet. 2021. PMID: 33337535 Free PMC article.
Craniofacial surgery in fibrous dysplasia.
Giordano F, Serio P, Savasta S, Oliveri G, Genitori L. Giordano F, et al. J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:595-604. doi: 10.1515/jpem.2006.19.s2.595. J Pediatr Endocrinol Metab. 2006. PMID: 16789622
Hox-D genes expression in pediatric low-grade gliomas: real-time-PCR study.
Buccoliero AM, Castiglione F, Rossi Degl'Innocenti D, Ammanati F, Giordano F, Sanzo M, Mussa F, Genitori L, Taddei GL. Buccoliero AM, et al. Among authors: giordano f. Cell Mol Neurobiol. 2009 Feb;29(1):1-6. doi: 10.1007/s10571-008-9282-1. Epub 2008 Apr 11. Cell Mol Neurobiol. 2009. PMID: 18404365
Surgical treatment of central nervous system malformations.
Genitori L, Donati PA, Giordano F, Sanzo M, Mussa F, Sardo L, Spacca B, di Pietro G, Oliveri G. Genitori L, et al. Among authors: giordano f. Handb Clin Neurol. 2008;87:569-90. doi: 10.1016/S0072-9752(07)87031-X. Handb Clin Neurol. 2008. PMID: 18809045 Review. No abstract available.
1,144 results