Fusco L - Search Results

1

Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions gene.

Malafosse A, Beck C, Bellet H, Di Capua M, Dulac O, Echenne B, Fusco L, Lucchini P, Ricci S, Sebastianelli R, et al. Malafosse A, et al. Among authors: fusco l. Ann Neurol. 1994 Apr;35(4):479-82. doi: 10.1002/ana.410350417. Ann Neurol. 1994. PMID: 8154876

2

Benign infantile familial convulsions.

Vigevano F, Fusco L, Di Capua M, Ricci S, Sebastianelli R, Lucchini P. Vigevano F, et al. Among authors: fusco l. Eur J Pediatr. 1992 Aug;151(8):608-12. doi: 10.1007/BF01957732. Eur J Pediatr. 1992. PMID: 1505581

3

Sixth-month benign familial convulsions.

Vigevano F, Di Capua M, Fusco L, Ricci S, Sebastianelli R, Lucchini P. Vigevano F, et al. Among authors: fusco l. Epilepsy Res Suppl. 1992;6:127-9. Epilepsy Res Suppl. 1992. PMID: 1418471 No abstract available.

4

Benign neonatal sleep myoclonus: clinical features and video-polygraphic recordings.

Di Capua M, Fusco L, Ricci S, Vigevano F. Di Capua M, et al. Among authors: fusco l. Mov Disord. 1993 Apr;8(2):191-4. doi: 10.1002/mds.870080213. Mov Disord. 1993. PMID: 8474488

5

Double cortex. A neuronal migration anomaly as a possible cause of Lennox-Gastaut syndrome.

Ricci S, Cusmai R, Fariello G, Fusco L, Vigevano F. Ricci S, et al. Among authors: fusco l. Arch Neurol. 1992 Jan;49(1):61-4. doi: 10.1001/archneur.1992.00530250065017. Arch Neurol. 1992. PMID: 1728265

6

Reflex myoclonic epilepsy in infancy: a new age-dependent idiopathic epileptic syndrome related to startle reaction.

Ricci S, Cusmai R, Fusco L, Vigevano F. Ricci S, et al. Among authors: fusco l. Epilepsia. 1995 Apr;36(4):342-8. doi: 10.1111/j.1528-1157.1995.tb01007.x. Epilepsia. 1995. PMID: 7607111

7

Video/EEG aspects of early-infantile epileptic encephalopathy with suppression-bursts (Ohtahara syndrome).

Fusco L, Pachatz C, Di Capua M, Vigevano F. Fusco L, et al. Brain Dev. 2001 Nov;23(7):708-14. doi: 10.1016/s0387-7604(01)00280-7. Brain Dev. 2001. PMID: 11701283

8

The idiopathic form of West syndrome.

Vigevano F, Fusco L, Cusmai R, Claps D, Ricci S, Milani L. Vigevano F, et al. Among authors: fusco l. Epilepsia. 1993 Jul-Aug;34(4):743-6. doi: 10.1111/j.1528-1157.1993.tb00456.x. Epilepsia. 1993. PMID: 8330587

9

PRRT2 is mutated in familial and non-familial benign infantile seizures.

Specchio N, Terracciano A, Trivisano M, Cappelletti S, Claps D, Travaglini L, Cusmai R, Marras CE, Zara F, Fusco L, Bertini E, Vigevano F. Specchio N, et al. Among authors: fusco l. Eur J Paediatr Neurol. 2013 Jan;17(1):77-81. doi: 10.1016/j.ejpn.2012.07.006. Epub 2012 Aug 17. Eur J Paediatr Neurol. 2013. PMID: 22902423

10

Ring 21 chromosome presenting with epilepsy and intellectual disability: clinical report and review of the literature.

Specchio N, Carotenuto A, Trivisano M, Cappelletti S, Digilio C, Capolino R, Di Capua M, Fusco L, Vigevano F. Specchio N, et al. Among authors: fusco l. Am J Med Genet A. 2011 Apr;155A(4):911-4. doi: 10.1002/ajmg.a.33899. Epub 2011 Mar 15. Am J Med Genet A. 2011. PMID: 21595005 Review. No abstract available.

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