Toldo I - Search Results

1

Epilepsy in NF1: Epidemiologic, Genetic, and Clinical Features. A Monocentric Retrospective Study in a Cohort of 784 Patients.

Sorrentino U, Bellonzi S, Mozzato C, Brasson V, Toldo I, Parrozzani R, Clementi M, Cassina M, Trevisson E. Sorrentino U, et al. Among authors: toldo i. Cancers (Basel). 2021 Dec 17;13(24):6336. doi: 10.3390/cancers13246336. Cancers (Basel). 2021. PMID: 34944956 Free PMC article.

2

Cold-Stimulus Headache in Children and Adolescents.

Bonemazzi I, Pelizza MF, Berti G, Ancona C, Nosadini M, Sartori S, Toldo I. Bonemazzi I, et al. Among authors: toldo i. Life (Basel). 2023 Apr 9;13(4):973. doi: 10.3390/life13040973. Life (Basel). 2023. PMID: 37109502 Free PMC article. Review.

3

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

4

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

5

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

6

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. 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.

7

Migraine therapy during pregnancy and lactation.

Cassina M, Di Gianantonio E, Toldo I, Battistella PA, Clementi M. Cassina M, et al. Among authors: toldo i. Expert Opin Drug Saf. 2010 Nov;9(6):937-48. doi: 10.1517/14740338.2010.505601. Expert Opin Drug Saf. 2010. PMID: 20662551

8

Polymorphisms of the SCN1A gene in children and adolescents with primary headache and idiopathic or cryptogenic epilepsy: is there a linkage?

Toldo I, Bruson A, Casarin A, Salviati L, Boniver C, Sartori S, Montagna P, Battistella PA, Clementi M. Toldo I, et al. J Headache Pain. 2011 Aug;12(4):435-41. doi: 10.1007/s10194-011-0359-8. Epub 2011 Jun 29. J Headache Pain. 2011. PMID: 21713554 Free PMC article.

9

Eating-induced epileptic spasms in a boy with MECP2 duplication syndrome: insights into pathogenesis of genetic epilepsies.

de Palma L, Boniver C, Cassina M, Toldo I, Nosadini M, Clementi M, Sartori S. de Palma L, et al. Among authors: toldo i. Epileptic Disord. 2012 Dec;14(4):414-7. doi: 10.1684/epd.2012.0546. Epileptic Disord. 2012. PMID: 23248047 Free article.

10

De novo trisomy 20p characterized by array comparative genomic hybridization: report of a novel case and review of the literature.

Bartolini L, Sartori S, Lenzini E, Rigon C, Cainelli E, Agrati C, Toldo I, Donà M, Trevisson E. Bartolini L, et al. Among authors: toldo i. Gene. 2013 Jul 25;524(2):368-72. doi: 10.1016/j.gene.2013.04.033. Epub 2013 Apr 21. Gene. 2013. PMID: 23612255 Review.

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