Toldo I - Search Results

1

Primary Stabbing Headache in Children and Adolescents.

Reimers M, Bonemazzi I, Brunello F, Cavaliere E, Sartori S, Toldo I. Reimers M, et al. Among authors: toldo i. Life (Basel). 2024 Feb 2;14(2):216. doi: 10.3390/life14020216. Life (Basel). 2024. PMID: 38398725 Free PMC article. Review.

2

Pleiotropic effects of spastin on neurite growth depending on expression levels.

Riano E, Martignoni M, Mancuso G, Cartelli D, Crippa F, Toldo I, Siciliano G, Di Bella D, Taroni F, Bassi MT, Cappelletti G, Rugarli EI. Riano E, et al. Among authors: toldo i. J Neurochem. 2009 Mar;108(5):1277-88. doi: 10.1111/j.1471-4159.2009.05875.x. Epub 2009 Jan 29. J Neurochem. 2009. PMID: 19141076 Free article.

3

Headache and recurrent abdominal pains in preschool children.

Battistella PA, Toldo I. Battistella PA, et al. Among authors: toldo i. J Headache Pain. 2006 Oct;7(5):322-3. doi: 10.1007/s10194-006-0321-3. J Headache Pain. 2006. PMID: 17058047 Free PMC article. No abstract available.

4

The role of visual evoked potentials in the differential diagnosis of functional visual loss and optic neuritis in children.

Suppiej A, Gaspa G, Cappellari A, Toldo I, Battistella PA. Suppiej A, et al. Among authors: toldo i. J Child Neurol. 2011 Jan;26(1):58-64. doi: 10.1177/0883073810373947. Epub 2010 Jun 29. J Child Neurol. 2011. PMID: 20587737

5

Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novel ASL pseudogene.

Trevisson E, Salviati L, Baldoin MC, Toldo I, Casarin A, Sacconi S, Cesaro L, Basso G, Burlina AB. Trevisson E, et al. Among authors: toldo i. Hum Mutat. 2007 Jul;28(7):694-702. doi: 10.1002/humu.20498. Hum Mutat. 2007. PMID: 17326097

6

The Pitt-Hopkins syndrome: report of 16 new patients and clinical diagnostic criteria.

Marangi G, Ricciardi S, Orteschi D, Lattante S, Murdolo M, Dallapiccola B, Biscione C, Lecce R, Chiurazzi P, Romano C, Greco D, Pettinato R, Sorge G, Pantaleoni C, Alfei E, Toldo I, Magnani C, Bonanni P, Martinez F, Serra G, Battaglia D, Lettori D, Vasco G, Baroncini A, Daolio C, Zollino M. Marangi G, et al. Among authors: toldo i. Am J Med Genet A. 2011 Jul;155A(7):1536-45. doi: 10.1002/ajmg.a.34070. Epub 2011 Jun 10. Am J Med Genet A. 2011. PMID: 21671391

7

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: toldo i. Neurogenetics. 2007 Jan;8(1):57-60. doi: 10.1007/s10048-006-0065-x. Epub 2006 Oct 10. Neurogenetics. 2007. PMID: 17031678

8

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. Among authors: toldo i. 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

9

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. Among authors: toldo i. J Child Neurol. 2008 Aug;23(8):912-5. doi: 10.1177/0883073808316367. Epub 2008 May 16. J Child Neurol. 2008. PMID: 18487518

10

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. Among authors: toldo i. Mov Disord. 2008 Aug 15;23(11):1605-8. doi: 10.1002/mds.22180. Mov Disord. 2008. PMID: 18618665

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