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Dyslexia and Attention Deficit Hyperactivity Disorder Associated to a De Novo 1p34.3 Microdeletion.
Genes (Basel). 2022 Oct 23;13(11):1926. doi: 10.3390/genes13111926.
Genes (Basel). 2022.
PMID: 36360163
Free PMC article.
Seizures and EEG pattern in the 22q13.3 deletion syndrome: clinical report of six Italian cases.
Figura MG, Coppola A, Bottitta M, Calabrese G, Grillo L, Luciano D, Del Gaudio L, Torniero C, Striano S, Elia M.
Figura MG, et al.
Seizure. 2014 Oct;23(9):774-9. doi: 10.1016/j.seizure.2014.06.008. Epub 2014 Jul 1.
Seizure. 2014.
PMID: 25027555
Free article.
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Mutation spectrum of NF1 gene in Italian patients with neurofibromatosis type 1 using Ion Torrent PGM™ platform.
Calì F, Chiavetta V, Ruggeri G, Piccione M, Selicorni A, Palazzo D, Bonsignore M, Cereda A, Elia M, Failla P, Figura MG, Fiumara A, Maitz S, Luana Mandarà GM, Mattina T, Ragalmuto A, Romano C, Ruggieri M, Salluzzo R, Saporoso A, Schepis C, Sorge G, Spanò M, Tortorella G, Romano V.
Calì F, et al. Among authors: figura mg.
Eur J Med Genet. 2017 Feb;60(2):93-99. doi: 10.1016/j.ejmg.2016.11.001. Epub 2016 Nov 9.
Eur J Med Genet. 2017.
PMID: 27838393
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Sleep and Headache.
Dosi C, Figura M, Ferri R, Bruni O.
Dosi C, et al.
Semin Pediatr Neurol. 2015 Jun;22(2):105-12. doi: 10.1016/j.spen.2015.04.005. Epub 2015 Apr 16.
Semin Pediatr Neurol. 2015.
PMID: 26072340
Review.
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