Ruggieri M - Search Results

1

Complex malformation (Ruggieri-Happle) phenotype with "cutis tricolor" in a 10-year-old girl.

Nicita F, Spalice A, Roggini M, Papetti L, Ursitti F, Tarani L, Ruggieri M. Nicita F, et al. Among authors: ruggieri m. Brain Dev. 2012 Nov;34(10):869-72. doi: 10.1016/j.braindev.2012.01.015. Epub 2012 Feb 26. Brain Dev. 2012. PMID: 22370055

2

Cutis tricolor: congenital hyper- and hypopigmented lesions in a background of normal skin with and without associated systemic features: further expansion of the phenotype.

Ruggieri M. Ruggieri M. Eur J Pediatr. 2000 Oct;159(10):745-9. doi: 10.1007/pl00008339. Eur J Pediatr. 2000. PMID: 11039129

3

Bilateral periventricular nodular heterotopia with amniotic band syndrome.

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

4

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. 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

5

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: ruggieri m. 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

6

Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke.

Barbagallo M, Pavone P, Incorpora G, Domenico Praticò A, Romantshik O, Friso S, Spalice A, Nicita F, Polizzi A, Ruggieri M, Iannetti P. Barbagallo M, et al. Among authors: ruggieri m. Childs Nerv Syst. 2009 Mar;25(3):361-5. doi: 10.1007/s00381-008-0724-3. Epub 2008 Oct 29. Childs Nerv Syst. 2009. PMID: 18958479

7

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: ruggieri m. 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

8

Addition of verapamil in the treatment of severe myoclonic epilepsy in infancy.

Iannetti P, Parisi P, Spalice A, Ruggieri M, Zara F. Iannetti P, et al. Among authors: ruggieri m. Epilepsy Res. 2009 Jul;85(1):89-95. doi: 10.1016/j.eplepsyres.2009.02.014. Epub 2009 Mar 20. Epilepsy Res. 2009. PMID: 19303743

9

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

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

10

Stroke in children: inherited and acquired factors and age-related variations in the presentation of 48 paediatric patients.

Del Balzo F, Spalice A, Ruggieri M, Greco F, Properzi E, Iannetti P. Del Balzo F, et al. Among authors: ruggieri m. Acta Paediatr. 2009 Jul;98(7):1130-6. doi: 10.1111/j.1651-2227.2009.01290.x. Epub 2009 Apr 30. Acta Paediatr. 2009. PMID: 19432826

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