Iannetti P - Search Results

1

Delineation of a newly recognized neurocutaneous malformation syndrome with "cutis tricolor".

Ruggieri M, Iannetti P, Pavone L. Ruggieri M, et al. Among authors: iannetti p. Am J Med Genet A. 2003 Jul 1;120A(1):110-6. doi: 10.1002/ajmg.a.20011. Am J Med Genet A. 2003. PMID: 12794702

2

Bilateral periventricular nodular heterotopia with amniotic band syndrome.

Ruggieri M, Spalice A, Polizzi A, Roggini M, Iannetti P. Ruggieri M, et al. Among authors: iannetti p. Pediatr Neurol. 2007 Jun;36(6):407-10. doi: 10.1016/j.pediatrneurol.2007.02.006. Pediatr Neurol. 2007. PMID: 17560504

3

Infantile spasms in the setting of Sturge-Weber syndrome.

Barbagallo M, Ruggieri M, Incorpora G, Pavone P, Nucifora C, Spalice A, Praticò AD, Polizzi A, Pavone L, Iannetti P. Barbagallo M, et al. Among authors: iannetti p. Childs Nerv Syst. 2009 Jan;25(1):111-8. doi: 10.1007/s00381-008-0705-6. Epub 2008 Oct 2. Childs Nerv Syst. 2009. PMID: 18830609

4

Pigmentary mosaicism, subcortical band heterotopia, and brain cystic lesions.

Ruggieri M, Roggini M, Spalice A, Addis M, Iannetti P. Ruggieri M, et al. Among authors: iannetti p. Pediatr Neurol. 2009 May;40(5):383-6. doi: 10.1016/j.pediatrneurol.2008.11.006. Pediatr Neurol. 2009. PMID: 19380077

5

Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1.

Ruggieri M, Mastrangelo M, Spalice A, Mariani R, Torrente I, Polizzi A, Bottillo I, Di Biase C, Iannetti P. Ruggieri M, et al. Among authors: iannetti p. Am J Med Genet A. 2011 Mar;155A(3):582-5. doi: 10.1002/ajmg.a.33318. Epub 2011 Feb 22. Am J Med Genet A. 2011. PMID: 21344624

6

Septo-optic dysplasia complex: a heterogeneous malformation syndrome.

Polizzi A, Pavone P, Iannetti P, Manfré L, Ruggieri M. Polizzi A, et al. Among authors: iannetti p. Pediatr Neurol. 2006 Jan;34(1):66-71. doi: 10.1016/j.pediatrneurol.2005.07.004. Pediatr Neurol. 2006. PMID: 16376284

7

Multiple sclerosis in children under 10 years of age.

Ruggieri M, Iannetti P, Polizzi A, Pavone L, Grimaldi LM; Italian Society of Paediatric Neurology Study Group on Childhood Multiple Sclerosis. Ruggieri M, et al. Among authors: iannetti p. Neurol Sci. 2004 Nov;25 Suppl 4:S326-35. doi: 10.1007/s10072-004-0335-z. Neurol Sci. 2004. PMID: 15727227 Review.

8

Earliest clinical manifestations and natural history of neurofibromatosis type 2 (NF2) in childhood: a study of 24 patients.

Ruggieri M, Iannetti P, Polizzi A, La Mantia I, Spalice A, Giliberto O, Platania N, Gabriele AL, Albanese V, Pavone L. Ruggieri M, et al. Among authors: iannetti p. Neuropediatrics. 2005 Feb;36(1):21-34. doi: 10.1055/s-2005-837581. Neuropediatrics. 2005. PMID: 15776319

9

Neurofibromatosis type 1 and infantile spasms.

Ruggieri M, Iannetti P, Clementi M, Polizzi A, Incorpora G, Spalice A, Pavone P, Praticò AD, Elia M, Gabriele AL, Tenconi R, Pavone L. Ruggieri M, et al. Among authors: iannetti p. Childs Nerv Syst. 2009 Feb;25(2):211-6. doi: 10.1007/s00381-008-0706-5. Epub 2008 Sep 19. Childs Nerv Syst. 2009. PMID: 18802710

10

Complex epileptic (Foix-Chavany-Marie like) syndrome in a child with neurofibromatosis type 1 (NF1) and bilateral (opercular and paracentral) polymicrogyria.

Mastrangelo M, Mariani R, Spalice A, Ruggieri M, Iannetti P. Mastrangelo M, et al. Among authors: iannetti p. Acta Paediatr. 2009 Apr;98(4):760-2. doi: 10.1111/j.1651-2227.2008.01183.x. Epub 2008 Jan 6. Acta Paediatr. 2009. PMID: 19141142

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