Fontana E - Search Results

1

Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys.

Mei D, Darra F, Barba C, Marini C, Fontana E, Chiti L, Parrini E, Dalla Bernardina B, Guerrini R. Mei D, et al. Among authors: fontana e. Epilepsia. 2014 Nov;55(11):1748-53. doi: 10.1111/epi.12803. Epub 2014 Sep 29. Epilepsia. 2014. PMID: 25266480 Free article.

2

Status epilepticus in benign rolandic epilepsy manifesting as anterior operculum syndrome.

Colamaria V, Sgrò V, Caraballo R, Simeone M, Zullini E, Fontana E, Zanetti R, Grimau-Merino R, Dalla Bernardina B. Colamaria V, et al. Among authors: fontana e. Epilepsia. 1991 May-Jun;32(3):329-34. doi: 10.1111/j.1528-1157.1991.tb04659.x. Epilepsia. 1991. PMID: 1904343

3

Efficacy and tolerability of vigabatrin in children with refractory partial seizures: a single-blind dose-increasing study.

Dalla Bernardina B, Fontana E, Vigevano F, Fusco L, Torelli D, Galeone D, Buti D, Cianchetti C, Gnanasakthy A, Iudice A. Dalla Bernardina B, et al. Among authors: fontana e. Epilepsia. 1995 Jul;36(7):687-91. doi: 10.1111/j.1528-1157.1995.tb01047.x. Epilepsia. 1995. PMID: 7555986 Clinical Trial.

4

Myoclonic status in nonprogressive encephalopathies.

Dalla Bernardina B, Fontana E, Darra F. Dalla Bernardina B, et al. Among authors: fontana e. Adv Neurol. 2005;95:59-70. Adv Neurol. 2005. PMID: 15508914 Review. No abstract available.

5

Temporal lobe epilepsy in children: electroclinical study of 77 cases.

Fontana E, Negrini F, Francione S, Mai R, Osanni E, Menna E, Offredi F, Darra F, Bernardina BD. Fontana E, et al. Epilepsia. 2006;47 Suppl 5:26-30. doi: 10.1111/j.1528-1167.2006.00873.x. Epilepsia. 2006. PMID: 17239102 Free article.

6

Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases.

Darra F, Fiorini E, Zoccante L, Mastella L, Torniero C, Cortese S, Meneghello L, Fontana E, Bernardina BD. Darra F, et al. Among authors: fontana e. Epilepsia. 2006;47 Suppl 5:31-5. doi: 10.1111/j.1528-1167.2006.00874.x. Epilepsia. 2006. PMID: 17239103 Free article.

7

Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients.

Caraballo RH, Fontana E, Darra F, Cassar L, Negrini F, Fiorini E, Arroyo H, Ferraro S, Fejerman N, Dalla Bernardina B. Caraballo RH, et al. Among authors: fontana e. J Child Neurol. 2008 May;23(5):497-506. doi: 10.1177/0883073807309771. Epub 2008 Jan 29. J Child Neurol. 2008. PMID: 18230844

8

Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations.

Caraballo RH, Fontana E, Darra F, Bongiorni L, Fiorini E, Cersosimo R, Fejerman N, Bernardinab BD. Caraballo RH, et al. Among authors: fontana e. Seizure. 2008 Oct;17(7):617-24. doi: 10.1016/j.seizure.2008.03.009. Seizure. 2008. PMID: 18524634 Free article.

9

A study of 63 cases with eyelid myoclonia with or without absences: type of seizure or an epileptic syndrome?

Caraballo RH, Fontana E, Darra F, Chacon S, Ross N, Fiorini E, Fejerman N, Dalla Bernardina B. Caraballo RH, et al. Among authors: fontana e. Seizure. 2009 Jul;18(6):440-5. doi: 10.1016/j.seizure.2009.04.004. Epub 2009 May 5. Seizure. 2009. PMID: 19419888 Free article.

10

Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathy.

Mei D, Marini C, Novara F, Bernardina BD, Granata T, Fontana E, Parrini E, Ferrari AR, Murgia A, Zuffardi O, Guerrini R. Mei D, et al. Among authors: fontana e. Epilepsia. 2010 Apr;51(4):647-54. doi: 10.1111/j.1528-1167.2009.02308.x. Epub 2009 Sep 22. Epilepsia. 2010. PMID: 19780792 Free article.

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