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Page 1
Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22.13q22.3) in a patient with dysmorphic features, intellectual disability and severe generalized epilepsy.
Valetto A, Orsini A, Bertini V, Toschi B, Bonuccelli A, Simi F, Sammartino I, Taddeucci G, Simi P, Saggese G. Valetto A, et al. Among authors: orsini a. Eur J Med Genet. 2012 May;55(5):362-6. doi: 10.1016/j.ejmg.2012.03.011. Epub 2012 Apr 24. Eur J Med Genet. 2012. PMID: 22548977
17q12 microduplications: a challenge for clinicians.
Bertini V, Orsini A, Bonuccelli A, Cambi F, Del Pistoia M, Vannozzi I, Toschi B, Saggese G, Simi P, Valetto A. Bertini V, et al. Among authors: orsini a. Am J Med Genet A. 2015 Mar;167A(3):674-6. doi: 10.1002/ajmg.a.36905. Am J Med Genet A. 2015. PMID: 25691423
Maternally derived 15q11.2-q13.1 duplication in a child with Lennox-Gastaut-type epilepsy and dysmorphic features: Clinical-genetic characterization of the family and review of the literature.
Bonuccelli A, Valetto A, Orsini A, Michelucci A, Ferrari AR, Elia M, Bertini V. Bonuccelli A, et al. Among authors: orsini a. Am J Med Genet A. 2017 Feb;173(2):556-560. doi: 10.1002/ajmg.a.38039. Epub 2016 Nov 14. Am J Med Genet A. 2017. PMID: 27862928 No abstract available.
Mothers and fathers of children with epilepsy: gender differences in post-traumatic stress symptoms and correlations with mood spectrum symptoms.
Carmassi C, Corsi M, Bertelloni CA, Carpita B, Gesi C, Pedrinelli V, Massimetti G, Peroni DG, Bonuccelli A, Orsini A, Dell'Osso L. Carmassi C, et al. Among authors: orsini a. Neuropsychiatr Dis Treat. 2018 May 25;14:1371-1379. doi: 10.2147/NDT.S158249. eCollection 2018. Neuropsychiatr Dis Treat. 2018. PMID: 29872304 Free PMC article.
534 results