Sartori S - Search Results

1

Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study.

Toldo I, Brunello F, Cavasin P, Nosadini M, Sartori S, Frigo AC, Mai R, Pelliccia V, Mancardi MM, Striano P, Severino M, Zara F, Rizzi R, Casellato S, Di Rosa G, Mastrangelo M, Spalice A, Budetta M, De Palma L, Guerrini R, Pruna D, Cordelli DM, Sofia V, Papa A, Chiesa V, Ragona F, Parisi P, D'Aniello A, Veggiotti P, Dainese F, Giordano L, Licchetta L, Tinuper P, D'Orsi G, Cassina M, Manara R. Toldo I, et al. Among authors: sartori s. Pediatr Neurol. 2023 Apr;141:58-64. doi: 10.1016/j.pediatrneurol.2023.01.012. Epub 2023 Jan 24. Pediatr Neurol. 2023. PMID: 36773408 Free article.

2

A novel deletion in the GJA12 gene causes Pelizaeus-Merzbacher-like disease.

Salviati L, Trevisson E, Baldoin MC, Toldo I, Sartori S, Calderone M, Tenconi R, Laverda A. Salviati L, et al. Among authors: sartori s. Neurogenetics. 2007 Jan;8(1):57-60. doi: 10.1007/s10048-006-0065-x. Epub 2006 Oct 10. Neurogenetics. 2007. PMID: 17031678

3

Increased level of N-acetylaspartylglutamate (NAAG) in the CSF of a patient with Pelizaeus-Merzbacher-like disease due to mutation in the GJA12 gene.

Sartori S, Burlina AB, Salviati L, Trevisson E, Toldo I, Laverda AM, Burlina AP. Sartori S, et al. Eur J Paediatr Neurol. 2008 Jul;12(4):348-50. doi: 10.1016/j.ejpn.2007.07.011. Epub 2007 Sep 18. Eur J Paediatr Neurol. 2008. PMID: 17881259

4

Angelman syndrome due to a novel splicing mutation of the UBE3A gene.

Sartori S, Anesi L, Polli R, Toldo I, Casarin A, Drigo P, Murgia A. Sartori S, et al. J Child Neurol. 2008 Aug;23(8):912-5. doi: 10.1177/0883073808316367. Epub 2008 May 16. J Child Neurol. 2008. PMID: 18487518

5

Benign nocturnal alternating hemiplegia of childhood: The first clinical report with paroxysmal events home-video recordings.

Sartori S, Vecchi M, Toldo I, Boniver C, Dalla Bernardina B, Maria Laverda A. Sartori S, et al. Mov Disord. 2008 Aug 15;23(11):1605-8. doi: 10.1002/mds.22180. Mov Disord. 2008. PMID: 18618665

6

Unilateral hypoglossal nerve palsy due to neurovascular conflict in a child.

Toldo I, Manara R, Sartori S, Suppiej A, Drigo P. Toldo I, et al. Among authors: sartori s. Brain Dev. 2009 Jun;31(6):461-4. doi: 10.1016/j.braindev.2008.08.009. Epub 2008 Sep 25. Brain Dev. 2009. PMID: 18819762

7

Diffusion-weighted imaging findings in hemolytic uremic syndrome with central nervous system involvement.

Toldo I, Manara R, Cogo P, Sartori S, Murer L, Battistella PA, Laverda AM. Toldo I, et al. Among authors: sartori s. J Child Neurol. 2009 Feb;24(2):247-50. doi: 10.1177/0883073808323022. Epub 2008 Dec 12. J Child Neurol. 2009. PMID: 19074752

8

A novel CDKL5 mutation in a 47,XXY boy with the early-onset seizure variant of Rett syndrome.

Sartori S, Di Rosa G, Polli R, Bettella E, Tricomi G, Tortorella G, Murgia A. Sartori S, et al. Am J Med Genet A. 2009 Feb;149A(2):232-6. doi: 10.1002/ajmg.a.32606. Am J Med Genet A. 2009. PMID: 19161156

9

Early cortical cytotoxic edema in meningococcal meningitis.

Citton V, Toldo I, Calderone M, Sartori S, Manara R. Citton V, et al. Among authors: sartori s. Pediatr Neurol. 2009 Aug;41(2):146-50. doi: 10.1016/j.pediatrneurol.2009.02.021. Pediatr Neurol. 2009. PMID: 19589467

10

Comorbidity between headache and epilepsy in a pediatric headache center.

Toldo I, Perissinotto E, Menegazzo F, Boniver C, Sartori S, Salviati L, Clementi M, Montagna P, Battistella PA. Toldo I, et al. Among authors: sartori s. J Headache Pain. 2010 Jun;11(3):235-40. doi: 10.1007/s10194-010-0191-6. Epub 2010 Jan 29. J Headache Pain. 2010. PMID: 20112041 Free PMC article.

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