Vigevano F - Search Results

1

Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR.

Terracciano A, Specchio N, Darra F, Sferra A, Bernardina BD, Vigevano F, Bertini E. Terracciano A, et al. Among authors: vigevano f. Neurogenetics. 2012 Nov;13(4):341-5. doi: 10.1007/s10048-012-0342-9. Epub 2012 Sep 6. Neurogenetics. 2012. PMID: 22949144

2

Epilepsia partialis continua and neuronal migration anomalies.

Fusco L, Bertini E, Vigevano F. Fusco L, et al. Among authors: vigevano f. Brain Dev. 1992 Sep;14(5):323-8. doi: 10.1016/s0387-7604(12)80152-5. Brain Dev. 1992. PMID: 1456388

3

Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothers.

Dionisi Vici C, Sabetta G, Gambarara M, Vigevano F, Bertini E, Boldrini R, Parisi SG, Quinti I, Aiuti F, Fiorilli M. Dionisi Vici C, et al. Among authors: vigevano f. Am J Med Genet. 1988 Jan;29(1):1-8. doi: 10.1002/ajmg.1320290102. Am J Med Genet. 1988. PMID: 3344762

4

Bilateral, reversible, selective thalamic involvement demonstrated by brain MR and acute severe neurological dysfunction with favorable outcome.

Cusmai R, Bertini E, Di Capua M, Ricci S, Vigevano F, Milani L, Fariello G. Cusmai R, et al. Among authors: vigevano f. Neuropediatrics. 1994 Feb;25(1):44-7. doi: 10.1055/s-2008-1071582. Neuropediatrics. 1994. PMID: 8208352

5

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.

Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F. Nabbout R, et al. Among authors: vigevano f. Neurology. 2003 Jun 24;60(12):1961-7. doi: 10.1212/01.wnl.0000069463.41870.2f. Neurology. 2003. PMID: 12821740

6

Experience with immunomodulatory treatments in Rasmussen's encephalitis.

Granata T, Fusco L, Gobbi G, Freri E, Ragona F, Broggi G, Mantegazza R, Giordano L, Villani F, Capovilla G, Vigevano F, Bernardina BD, Spreafico R, Antozzi C. Granata T, et al. Among authors: vigevano f. Neurology. 2003 Dec 23;61(12):1807-10. doi: 10.1212/01.wnl.0000099074.04539.e0. Neurology. 2003. PMID: 14694056

7

A novel SCN2A mutation in family with benign familial infantile seizures.

Striano P, Bordo L, Lispi ML, Specchio N, Minetti C, Vigevano F, Zara F. Striano P, et al. Among authors: vigevano f. Epilepsia. 2006 Jan;47(1):218-20. doi: 10.1111/j.1528-1167.2006.00392.x. Epilepsia. 2006. PMID: 16417554 Free article.

8

Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: Another genetic hit in the Mediterranean.

Cannelli N, Cassandrini D, Bertini E, Striano P, Fusco L, Gaggero R, Specchio N, Biancheri R, Vigevano F, Bruno C, Simonati A, Zara F, Santorelli FM. Cannelli N, et al. Among authors: vigevano f. Neurogenetics. 2006 May;7(2):111-7. doi: 10.1007/s10048-005-0024-y. Epub 2006 Mar 29. Neurogenetics. 2006. PMID: 16570191

9

Occurrence of a prolonged nonepileptic motor status after a febrile seizure.

Specchio N, Cusmai R, Volkov J, Montaldo P, Vigevano F. Specchio N, et al. Among authors: vigevano f. Epilepsia. 2006 Jun;47(6):1079-81. doi: 10.1111/j.1528-1167.2006.00578.x. Epilepsia. 2006. PMID: 16822258 Free article.

10

The spectrum of benign infantile seizures.

Specchio N, Vigevano F. Specchio N, et al. Among authors: vigevano f. Epilepsy Res. 2006 Aug;70 Suppl 1:S156-67. doi: 10.1016/j.eplepsyres.2006.01.018. Epub 2006 Jul 11. Epilepsy Res. 2006. PMID: 16837167 Review.

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