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Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation.
Taddeucci G, Bonuccelli A, Mantellassi I, Orsini A, Tarantino E. Taddeucci G, et al. Among authors: bonuccelli a. Ital J Pediatr. 2010 Feb 2;36:12. doi: 10.1186/1824-7288-36-12. Ital J Pediatr. 2010. PMID: 20205897 Free PMC article.
Acute myelitis in a child: current hypotheses.
Taddeucci G, Bonuccelli A, Polacco P. Taddeucci G, et al. Among authors: bonuccelli a. Pediatr Neurol. 2006 Dec;35(6):430-2. doi: 10.1016/j.pediatrneurol.2006.05.013. Pediatr Neurol. 2006. PMID: 17138014
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: bonuccelli 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: bonuccelli 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
63 results