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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: taddeucci g. 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
Acute myelitis in a child: current hypotheses.
Taddeucci G, Bonuccelli A, Polacco P. Taddeucci G, et al. Pediatr Neurol. 2006 Dec;35(6):430-2. doi: 10.1016/j.pediatrneurol.2006.05.013. Pediatr Neurol. 2006. PMID: 17138014
Radiological findings in a case of Menkes' disease.
Pinto F, Calderazzi A, Canapicchi R, Taddeucci G, Tarantino E. Pinto F, et al. Among authors: taddeucci g. Childs Nerv Syst. 1995 Feb;11(2):112-4. doi: 10.1007/BF00303816. Childs Nerv Syst. 1995. PMID: 7758009
[Gardner syndrome].
Tarantino E, Meozzi A, Villirillo A, Lamesa G, Taddeucci G. Tarantino E, et al. Among authors: taddeucci g. Pediatr Med Chir. 1995 Sep-Oct;17(5):473-7. Pediatr Med Chir. 1995. PMID: 8685009 Italian.
18 results