Striano P - Search Results

1

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

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

Small hypothalamic hamartomas and gelastic seizures.

Striano S, Striano P, Cirillo S, Nocerino C, Bilo L, Meo R, Ruosi P, Boccella P, Briganti F. Striano S, et al. Among authors: striano p. Epileptic Disord. 2002 Jun;4(2):129-33. Epileptic Disord. 2002. PMID: 12105075 Free article.

4

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

5

Posterior reversible encephalopathy syndrome (PRES) in critically ill obstetric patients.

Servillo G, Striano P, Striano S, Tortora F, Boccella P, De Robertis E, Rossano F, Briganti F, Tufano R. Servillo G, et al. Among authors: striano p, striano s. Intensive Care Med. 2003 Dec;29(12):2323-2326. doi: 10.1007/s00134-003-1901-1. Epub 2003 Aug 6. Intensive Care Med. 2003. PMID: 12904853

6

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.

7

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.

8

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

9

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.

10

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.

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