Savasta S - Search Results

1

Unilateral Lisch nodules in a pediatric patient: a sign for genetic mosaicism?

Orsini A, Santangelo A, Bonuccelli A, Ragone MC, Foiadelli T, Savasta S, Madia F, Peroni D, Striano P. Orsini A, et al. Among authors: savasta s. Minerva Pediatr (Torino). 2023 Feb;75(1):137-139. doi: 10.23736/S2724-5276.20.06134-4. Epub 2020 Nov 17. Minerva Pediatr (Torino). 2023. PMID: 33203204 No abstract available.

2

Epilepsy in patients with Cornelia de Lange syndrome: a clinical series.

Verrotti A, Agostinelli S, Prezioso G, Coppola G, Capovilla G, Romeo A, Striano P, Parisi P, Grosso S, Spalice A, Foiadelli T, Curatolo P, Chiarelli F, Savasta S. Verrotti A, et al. Among authors: savasta s. Seizure. 2013 Jun;22(5):356-9. doi: 10.1016/j.seizure.2013.01.017. Epub 2013 Mar 7. Seizure. 2013. PMID: 23473710 Free article.

3

Seizures in fetal alcohol spectrum disorders: evaluation of clinical, electroencephalographic, and neuroradiologic features in a pediatric case series.

Nicita F, Verrotti A, Pruna D, Striano P, Capovilla G, Savasta S, Spartà MV, Parisi P, Parlapiano G, Tarani L, Spalice A. Nicita F, et al. Among authors: savasta s. Epilepsia. 2014 Jun;55(6):e60-6. doi: 10.1111/epi.12638. Epub 2014 May 9. Epilepsia. 2014. PMID: 24815902 Free article.

4

Stickler syndrome associated with epilepsy: report of three cases.

Savasta S, Salpietro V, Spartà MV, Foiadelli T, Laino D, Lobefalo L, Marseglia GL, Verrotti A. Savasta S, et al. Eur J Pediatr. 2015 May;174(5):697-701. doi: 10.1007/s00431-015-2514-8. Epub 2015 Mar 27. Eur J Pediatr. 2015. PMID: 25809783

5

Unilateral periventricular heterotopia and epilepsy in a girl with Ehlers-Danlos syndrome.

Savasta S, Verrotti A, Spartà MV, Foiadelli T, Villa MP, Parisi P. Savasta S, et al. Epilepsy Behav Case Rep. 2015 Jun 14;4:27-9. doi: 10.1016/j.ebcr.2015.05.004. eCollection 2015. Epilepsy Behav Case Rep. 2015. PMID: 26110114 Free PMC article.

6

Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.

Nicita F, Garone G, Spalice A, Savasta S, Striano P, Pantaleoni C, Spartà MV, Kluger G, Capovilla G, Pruna D, Freri E, D'Arrigo S, Verrotti A. Nicita F, et al. Among authors: savasta s. Am J Med Genet A. 2016 Jan;170A(1):148-55. doi: 10.1002/ajmg.a.37410. Epub 2015 Oct 5. Am J Med Genet A. 2016. PMID: 26437767

7

Paediatric clinically isolated syndromes: report of seven cases, differential diagnosis and literature review.

Trabatti C, Foiadelli T, Spartà MV, Gagliardone C, Rinaldi B, Delmonte M, Lozza A, Savasta S. Trabatti C, et al. Among authors: savasta s. Childs Nerv Syst. 2016 Jan;32(1):69-77. doi: 10.1007/s00381-015-2959-0. Epub 2015 Nov 19. Childs Nerv Syst. 2016. PMID: 26584554 Review.

8

Nucleotide variation in Sabin type 3 poliovirus from an Albanian infant with agammaglobulinemia and vaccine associated poliomyelitis.

Foiadelli T, Savasta S, Battistone A, Kota M, Passera C, Fiore S, Bino S, Amato C, Lozza A, Marseglia GL, Fiore L. Foiadelli T, et al. Among authors: savasta s. BMC Infect Dis. 2016 Jun 10;16:277. doi: 10.1186/s12879-016-1587-y. BMC Infect Dis. 2016. PMID: 27287521 Free PMC article.

9

Postural analysis in a pediatric cohort of patients with Ehlers-Danlos Syndrome: a pilot study.

Lisi C, Monteleone S, Tinelli C, Rinaldi B, Di Natali G, Savasta S. Lisi C, et al. Among authors: savasta s. Minerva Pediatr. 2020 Apr;72(2):73-78. doi: 10.23736/S0026-4946.17.04681-3. Epub 2017 Feb 17. Minerva Pediatr. 2020. PMID: 28211643

10

Coexistence of childhood absence epilepsy and benign epilepsy with centrotemporal spikes: A case series.

Verrotti A, Casciato S, Spalice A, Carotenuto M, Striano P, Parisi P, Zamponi N, Savasta S, Rinaldi VE, D'Alonzo R, Mecarini F, Ritaccio AJ, Di Gennaro G. Verrotti A, et al. Among authors: savasta s. Eur J Paediatr Neurol. 2017 May;21(3):570-575. doi: 10.1016/j.ejpn.2017.02.002. Epub 2017 Feb 14. Eur J Paediatr Neurol. 2017. PMID: 28238620

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