G. Taddeucci

发表

Periventricular Nodular Heterotopia: Report of a Pediatric Series

A. Spalice, P. Iannetti, F. Perla, 2002, Journal of child neurology.

Pitt-Hopkins syndrome: report of a case with a TCF4 gene mutation

A. Orsini, E. Tarantino, A. Bonuccelli, 2010, Italian journal of pediatrics.

Pattern reversal evoked potentials in infantile spasms.

D. Spinelli, A. Fiorentini, M. Pirchio, 1984, Human neurobiology.

Migraine-like attacks in child with Sturge-Weber syndrome without facial nevus.

A. Bonuccelli, G. Taddeucci, Paola Polacco, 2005, Pediatric neurology.

Clinical pattern, mutations and in vitro residual activity in 33 patients with severe 5, 10 methylenetetrahydrofolate reductase (MTHFR) deficiency

M. Baumgartner, T. Suormala, P. Chinnery, 2016, Journal of Inherited Metabolic Disease.

Molecular cytogenetic characterization of a de novo mosaic supernumerary ring chromosome 7: Report of a new patient

P. Simi, E. Tarantino, V. Bertini, 2008, American journal of medical genetics. Part A.

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.

P. Simi, A. Orsini, G. Saggese, 2012, European journal of medical genetics.

β‐galactosidase gene mutations affecting the lysosomal enzyme and the elastin‐binding protein in GM1‐gangliosidosis patients with cardiac involvement

E. Zammarchi, M. Donati, A. Morrone, 2000, Human mutation.

[Diagnosis of coeliac disease in patients with isolated neuropsychological symptoms. Cases reports].

A. Bonuccelli, G. Taddeucci, Paola Polacco, 2005, La Pediatria medica e chirurgica : Medical and surgical pediatrics.

Bartonella henselae infection associated with Guillain-Barre syndrome.

L. Gori, G. Maggiore, P. Macchia, 2006, The Pediatric infectious disease journal.

Radiological findings in a case of Menkes' disease

R. Canapicchi, E. Tarantino, A. Calderazzi, 1995, Child's Nervous System.