Striano S - Search Results

1

17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome.

Bernardo P, Madia F, Santulli L, Del Gaudio L, Caccavale C, Zara F, Traverso M, Cirillo M, Striano S, Coppola A. Bernardo P, et al. Among authors: striano s. Brain Dev. 2016 Aug;38(7):663-8. doi: 10.1016/j.braindev.2016.02.002. Epub 2016 Feb 17. Brain Dev. 2016. PMID: 26897099

2

Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME.

de Falco FA, Striano P, de Falco A, Striano S, Santangelo R, Perretti A, Balbi P, Cecconi M, Zara F. de Falco FA, et al. Among authors: striano p, striano s. Neurology. 2003 Apr 22;60(8):1381-5. doi: 10.1212/01.wnl.0000055874.24000.4a. Neurology. 2003. PMID: 12707452

3

Bioptically demonstrated Lafora disease without EPM2A mutation: a clinical and neurophysiological study of two sisters.

Boccella P, Striano P, Zara F, Barbieri F, Sarappa C, Vacca G, de Falco FA, Striano S. Boccella P, et al. Among authors: striano p, striano s. Clin Neurol Neurosurg. 2003 Dec;106(1):55-9. doi: 10.1016/j.clineuro.2003.07.003. Clin Neurol Neurosurg. 2003. PMID: 14643920

4

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype.

Striano P, Zara F, Striano S. Striano P, et al. Among authors: striano s. Acta Neurol Scand. 2005 Apr;111(4):211-7. doi: 10.1111/j.1600-0404.2005.00385.x. Acta Neurol Scand. 2005. PMID: 15740570

5

Unfavourable outcome of Hashimoto encephalopathy due to status epilepticus. One autopsy case.

Striano P, Pagliuca M, Andreone V, Zara F, Coppola A, Striano S. Striano P, et al. Among authors: striano s. J Neurol. 2006 Feb;253(2):248-9. doi: 10.1007/s00415-005-0925-6. Epub 2005 Nov 22. J Neurol. 2006. PMID: 16328109 No abstract available.

6

Electroclinical and genetic findings in a family with cortical tremor, myoclonus, and epilepsy.

Striano P, Madia F, Minetti C, Striano S, Zara F. Striano P, et al. Among authors: striano s. Epilepsia. 2005 Dec;46(12):1993-5. doi: 10.1111/j.1528-1167.2005.00346.x. Epilepsia. 2005. PMID: 16393167 Free article.

7

Clinical and genetic findings in 26 Italian patients with Lafora disease.

Franceschetti S, Gambardella A, Canafoglia L, Striano P, Lohi H, Gennaro E, Ianzano L, Veggiotti P, Sofia V, Biondi R, Striano S, Gellera C, Annesi G, Madia F, Civitelli D, Rocca FE, Quattrone A, Avanzini G, Minassian B, Zara F. Franceschetti S, et al. Among authors: striano p, striano s. Epilepsia. 2006 Mar;47(3):640-3. doi: 10.1111/j.1528-1167.2006.00479.x. Epilepsia. 2006. PMID: 16529633 Free article.

8

Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study.

Striano P, Coppola A, Vacca G, Zara F, Brescia Morra V, Orefice G, Striano S. Striano P, et al. Among authors: striano s. J Neurol. 2006 Jun;253(6):762-6. doi: 10.1007/s00415-006-0112-4. Epub 2006 May 12. J Neurol. 2006. PMID: 16683063

9

6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.

Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F. Elia M, et al. Among authors: striano p, striano s. Epilepsia. 2006 May;47(5):830-8. doi: 10.1111/j.1528-1167.2006.00522.x. Epilepsia. 2006. PMID: 16686647 Free article.

10

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.

Striano P, Malacarne M, Cavani S, Pierluigi M, Rinaldi R, Cavaliere ML, Rinaldi MM, De Bernardo C, Coppola A, Pintaudi M, Gaggero R, Grammatico P, Striano S, Dallapiccola B, Zara F, Faravelli F. Striano P, et al. Among authors: striano s. Am J Med Genet A. 2006 Sep 15;140(18):1944-9. doi: 10.1002/ajmg.a.31435. Am J Med Genet A. 2006. PMID: 16906558

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