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Cerebellar atrophy in a child with hereditary methemoglobinemia type II.
Fusco C, Soncini G, Frattini D, Della Giustina E, Vercellati C, Fermo E, Bianchi P. Fusco C, et al. Among authors: della giustina e. Brain Dev. 2011 Apr;33(4):357-60. doi: 10.1016/j.braindev.2010.06.015. Epub 2010 Jul 22. Brain Dev. 2011. PMID: 20650578
"Minimal" holoprosencephaly in a 14q deletion syndrome patient.
Della Giustina E, Iodice A, Spagnoli C, Giovannini S, Frattini D, Fusco C, Gobbi G, Zollino M, Neri G. Della Giustina E, et al. Am J Med Genet A. 2017 Dec;173(12):3216-3220. doi: 10.1002/ajmg.a.38378. Am J Med Genet A. 2017. PMID: 29136354
Epilepsy in ring 14 syndrome: a clinical and EEG study of 22 patients.
Giovannini S, Marangio L, Fusco C, Scarano A, Frattini D, Della Giustina E, Zollino M, Neri G, Gobbi G. Giovannini S, et al. Among authors: della giustina e. Epilepsia. 2013 Dec;54(12):2204-13. doi: 10.1111/epi.12393. Epub 2013 Oct 1. Epilepsia. 2013. PMID: 24116895 Free article.
41 results