Clementi M - Search Results

1

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: clementi m. Epileptic Disord. 2012 Dec;14(4):414-7. doi: 10.1684/epd.2012.0546. Epileptic Disord. 2012. PMID: 23248047 Free article.

2

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: clementi m. 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.

3

Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3A.

Vecchi M, Cassina M, Casarin A, Rigon C, Drigo P, De Palma L, Clementi M. Vecchi M, et al. Among authors: clementi m. Seizure. 2011 Dec;20(10):813-6. doi: 10.1016/j.seizure.2011.07.008. Epub 2011 Sep 3. Seizure. 2011. PMID: 21893419 Free article.

4

Migraine therapy during pregnancy and lactation.

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

5

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. Among authors: clementi m. 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.

6

FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome.

Cassina M, Rigon C, Casarin A, Vicenzi V, Salviati L, Clementi M. Cassina M, et al. Among authors: clementi m. Am J Med Genet A. 2015 Jun;167(6):1418-20. doi: 10.1002/ajmg.a.37033. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25900767 No abstract available.

7

Human teratogens and genetic phenocopies. Understanding pathogenesis through human genes mutation.

Cassina M, Cagnoli GA, Zuccarello D, Di Gianantonio E, Clementi M. Cassina M, et al. Among authors: clementi m. Eur J Med Genet. 2017 Jan;60(1):22-31. doi: 10.1016/j.ejmg.2016.09.011. Epub 2016 Sep 14. Eur J Med Genet. 2017. PMID: 27639441

8

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: clementi m. Cancers (Basel). 2021 Dec 17;13(24):6336. doi: 10.3390/cancers13246336. Cancers (Basel). 2021. PMID: 34944956 Free PMC article.

9

Pharmacologic treatment of hyperthyroidism during pregnancy.

Cassina M, Donà M, Di Gianantonio E, Clementi M. Cassina M, et al. Among authors: clementi m. Birth Defects Res A Clin Mol Teratol. 2012 Aug;94(8):612-9. doi: 10.1002/bdra.23012. Epub 2012 Apr 18. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 22511519 Review.

10

A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus.

Zanetti A, Tomanin R, Rampazzo A, Rigon C, Gasparotto N, Cassina M, Clementi M, Scarpa M. Zanetti A, et al. Among authors: clementi m. JIMD Rep. 2014;17:13-21. doi: 10.1007/8904_2014_317. Epub 2014 Jul 25. JIMD Rep. 2014. PMID: 25059704 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

836 results

Search Page

Filters