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Expanding the phenotype of RTTN variations: a new family with primary microcephaly, severe growth failure, brain malformations and dermatitis.
Grandone A, Torella A, Santoro C, Giugliano T, Del Vecchio Blanco F, Mutarelli M, Cirillo M, Cirillo G, Piluso G, Capristo C, Festa A, Marzuillo P, Miraglia Del Giudice E, Perrone L, Nigro V. Grandone A, et al. Among authors: cirillo g, cirillo m. Clin Genet. 2016 Nov;90(5):445-450. doi: 10.1111/cge.12771. Epub 2016 Apr 29. Clin Genet. 2016. PMID: 26940245
Regional gray matter atrophy in patients with Parkinson disease and freezing of gait.
Tessitore A, Amboni M, Cirillo G, Corbo D, Picillo M, Russo A, Vitale C, Santangelo G, Erro R, Cirillo M, Esposito F, Barone P, Tedeschi G. Tessitore A, et al. Among authors: cirillo g, cirillo m. AJNR Am J Neuroradiol. 2012 Oct;33(9):1804-9. doi: 10.3174/ajnr.A3066. Epub 2012 Apr 26. AJNR Am J Neuroradiol. 2012. PMID: 22538070 Free PMC article.
Livedo and ischemic strokes: diagnostic hints of a rare condition.
Cirillo G, Tessitore A, Cirillo M, Salemi F, Liguori S, Esposito S, Tedeschi G. Cirillo G, et al. Among authors: cirillo m. Neurol Sci. 2013 Nov;34(11):2073-5. doi: 10.1007/s10072-013-1452-3. Epub 2013 May 10. Neurol Sci. 2013. PMID: 23660637 No abstract available.
Giant thrombosed intracavernous carotid artery aneurysm presenting as Tolosa-Hunt syndrome in a patient harboring a new pathogenic neurofibromatosis type 1 mutation: a case report and review of the literature.
Conforti R, Cirillo M, Marrone V, Galasso R, Capaldo G, Giugliano T, Scuotto A, Piluso G, Melone MA. Conforti R, et al. Among authors: cirillo m. Neuropsychiatr Dis Treat. 2014 Jan 20;10:135-40. doi: 10.2147/NDT.S49784. eCollection 2014. Neuropsychiatr Dis Treat. 2014. PMID: 24476631 Free PMC article.
LEOPARD syndrome: clinical dilemmas in differential diagnosis of RASopathies.
Santoro C, Pacileo G, Limongelli G, Scianguetta S, Giugliano T, Piluso G, Ragione FD, Cirillo M, Mirone G, Perrotta S. Santoro C, et al. Among authors: cirillo m. BMC Med Genet. 2014 Apr 26;15:44. doi: 10.1186/1471-2350-15-44. BMC Med Genet. 2014. PMID: 24767283 Free PMC article.
Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.
Santoro C, Di Rocco F, Kossorotoff M, Zerah M, Boddaert N, Calmon R, Vidaud D, Cirillo M, Cinalli G, Mirone G, Giugliano T, Piluso G, D'Amico A, Capra V, Pavanello M, Cama A, Nobili B, Lyonnet S, Perrotta S. Santoro C, et al. Among authors: cirillo m. Am J Med Genet A. 2017 Jun;173(6):1521-1530. doi: 10.1002/ajmg.a.38212. Epub 2017 Apr 19. Am J Med Genet A. 2017. PMID: 28422438
634 results