Striano P - Search Results

1

Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death.

Partemi S, Cestèle S, Pezzella M, Campuzano O, Paravidino R, Pascali VL, Zara F, Tassinari CA, Striano S, Oliva A, Brugada R, Mantegazza M, Striano P. Partemi S, et al. Among authors: striano p, striano s. Epilepsia. 2013 Aug;54(8):e112-6. doi: 10.1111/epi.12259. Epilepsia. 2013. PMID: 23899126 Free article.

2

Tiagabine in glial tumors.

Striano S, Striano P, Boccella P, Nocerino C, Bilo L. Striano S, et al. Among authors: striano p. Epilepsy Res. 2002 Mar;49(1):81-5. doi: 10.1016/s0920-1211(02)00005-0. Epilepsy Res. 2002. PMID: 11948010

3

Eyelid myoclonia with absences: an overlooked epileptic syndrome?

Striano S, Striano P, Nocerino C, Boccella P, Bilo L, Meo R, Ruosi P. Striano S, et al. Among authors: striano p. Neurophysiol Clin. 2002 Nov;32(5):287-96. doi: 10.1016/s0987-7053(02)00343-x. Neurophysiol Clin. 2002. PMID: 12490326

4

A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2.

Striano P, Chifari R, Striano S, de Fusco M, Elia M, Guerrini R, Casari G, Canevini MP. Striano P, et al. Among authors: striano s. Epilepsia. 2004 Feb;45(2):190-2. doi: 10.1111/j.0013-9580.2004.39903.x. Epilepsia. 2004. PMID: 14738428 Free article.

5

Spinal muscular atrophy and progressive myoclonic epilepsy: one case report and characteristics of the epileptic syndrome.

Striano P, Boccella P, Sarappa C, Striano S. Striano P, et al. Among authors: striano s. Seizure. 2004 Dec;13(8):582-6. doi: 10.1016/j.seizure.2004.01.008. Seizure. 2004. PMID: 15519918 Free article.

6

Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardation.

Coppola G, Criscuolo C, De Michele G, Striano S, Barbieri F, Striano P, Perretti A, Santoro L, Brescia Morra V, Saccà F, Scarano V, D'Adamo AP, Banfi S, Gasparini P, Santorelli FM, Lehesjoki AE, Filla A. Coppola G, et al. Among authors: striano p, striano s. J Neurol. 2005 Aug;252(8):897-900. doi: 10.1007/s00415-005-0766-3. Epub 2005 Mar 8. J Neurol. 2005. PMID: 15742102

7

The clinical spectrum and natural history of gelastic epilepsy-hypothalamic hamartoma syndrome.

Striano S, Striano P, Sarappa C, Boccella P. Striano S, et al. Among authors: striano p. Seizure. 2005 Jun;14(4):232-9. doi: 10.1016/j.seizure.2005.01.004. Seizure. 2005. PMID: 15911357 Free article.

8

A t(4;9)(q34;p22) translocation associated with partial epilepsy, mental retardation, and dysmorphism.

Striano P, Elia M, Castiglia L, Galesi O, Pelligra S, Striano S. Striano P, et al. Among authors: striano s. Epilepsia. 2005 Aug;46(8):1322-4. doi: 10.1111/j.1528-1167.2005.64304.x. Epilepsia. 2005. PMID: 16060948 Free article. No abstract available.

9

Levetiracetam in patients with cortical myoclonus: a clinical and electrophysiological study.

Striano P, Manganelli F, Boccella P, Perretti A, Striano S. Striano P, et al. Among authors: striano s. Mov Disord. 2005 Dec;20(12):1610-4. doi: 10.1002/mds.20530. Mov Disord. 2005. PMID: 16078205 Clinical Trial.

10

Late-onset and slow-progressing Lafora disease in four siblings with EPM2B mutation.

Baykan B, Striano P, Gianotti S, Bebek N, Gennaro E, Gurses C, Zara F. Baykan B, et al. Among authors: striano p. Epilepsia. 2005 Oct;46(10):1695-7. doi: 10.1111/j.1528-1167.2005.00272.x. Epilepsia. 2005. PMID: 16190947 Free article.

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