Striano S - Search Results

1

Inherited neuromyotonia: a clinical and genetic study of a family.

Falace A, Striano P, Manganelli F, Coppola A, Striano S, Minetti C, Zara F. Falace A, et al. Among authors: striano p, striano s. Neuromuscul Disord. 2007 Jan;17(1):23-7. doi: 10.1016/j.nmd.2006.09.014. Epub 2006 Nov 30. Neuromuscul Disord. 2007. PMID: 17140792

2

Eating epilepsy. Heterogeneity of ictal semiology: the role of video-EEG monitoring.

Loreto V, Nocerino C, Striano P, D' Aulos F, Boccella P, Striano S. Loreto V, et al. Among authors: striano p, striano s. Epileptic Disord. 2000 Jun;2(2):93-8. Epileptic Disord. 2000. PMID: 10954240 Free article.

3

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

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

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

6

Epilepsia partialis continua as a first symptom of multiple sclerosis: electrophysiological study of one case.

Striano P, Striano S, Carrieri PB, Boccella P. Striano P, et al. Among authors: striano s. Mult Scler. 2003 Mar;9(2):199-203. doi: 10.1191/1352458503ms866sr. Mult Scler. 2003. PMID: 12708815

7

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

8

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

9

Distal hypoglycemic neuropathy. An insulinoma-associated case, misdiagnosed as temporal lobe epilepsy.

Striano S, Striano P, Manganelli F, Boccella P, Bruno R, Santoro L, Percopo V. Striano S, et al. Among authors: striano p. Neurophysiol Clin. 2003 Nov;33(5):223-7. doi: 10.1016/j.neucli.2003.08.001. Neurophysiol Clin. 2003. PMID: 14672823

10

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.

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