Striano P - Search Results

1

Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy.

Ayerdi-Izquierdo A, Stavrides G, Sellés-Martínez JJ, Larrea L, Bovo G, López de Munain A, Bisulli F, Martí-Massó JF, Michelucci R, Poza JJ, Tinuper P, Stephani U, Striano P, Striano S, Staub E, Sarafidou T, Hinzmann B, Moschonas N, Siebert R, Deloukas P, Nobile C, Pérez-Tur J. Ayerdi-Izquierdo A, et al. Among authors: striano p, striano s. Epilepsy Res. 2006 Aug;70(2-3):118-26. doi: 10.1016/j.eplepsyres.2006.03.008. Epub 2006 May 16. Epilepsy Res. 2006. PMID: 16707245 Free article.

2

Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases.

Bisulli F, Tinuper P, Avoni P, Striano P, Striano S, d'Orsi G, Vignatelli L, Bagattin A, Scudellaro E, Florindo I, Nobile C, Tassinari CA, Baruzzi A, Michelucci R. Bisulli F, et al. Among authors: striano p, striano s. Brain. 2004 Jun;127(Pt 6):1343-52. doi: 10.1093/brain/awh151. Epub 2004 Apr 16. Brain. 2004. PMID: 15090473 Review.

3

Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation.

Striano P, Busolin G, Santulli L, Leonardi E, Coppola A, Vitiello L, Rigon L, Michelucci R, Tosatto SC, Striano S, Nobile C. Striano P, et al. Among authors: striano s. Neurology. 2011 Mar 29;76(13):1173-6. doi: 10.1212/WNL.0b013e318212ab2e. Neurology. 2011. PMID: 21444903

4

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.

Michelucci R, Mecarelli O, Bovo G, Bisulli F, Testoni S, Striano P, Striano S, Tinuper P, Nobile C. Michelucci R, et al. Among authors: striano p, striano s. Neurology. 2007 Jun 12;68(24):2150-1. doi: 10.1212/01.wnl.0000264932.44153.3c. Neurology. 2007. PMID: 17562837 No abstract available.

5

LGI1 microdeletion in autosomal dominant lateral temporal epilepsy.

Fanciulli M, Santulli L, Errichiello L, Barozzi C, Tomasi L, Rigon L, Cubeddu T, de Falco A, Rampazzo A, Michelucci R, Uzzau S, Striano S, de Falco FA, Striano P, Nobile C. Fanciulli M, et al. Among authors: striano p, striano s. Neurology. 2012 Apr 24;78(17):1299-303. doi: 10.1212/WNL.0b013e3182518328. Epub 2012 Apr 11. Neurology. 2012. PMID: 22496201 Free PMC article.

6

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

7

Whole-genome linkage scan for epilepsy-related photosensitivity: a mega-analysis.

de Kovel CG, Pinto D, Tauer U, Lorenz S, Muhle H, Leu C, Neubauer BA, Hempelmann A, Callenbach PM, Scheffer IE, Berkovic SF, Rudolf G, Striano P, Siren A, Baykan B, Sander T, Lindhout D, Kasteleijn-Nolst Trenité DG, Stephani U, Koeleman BP. de Kovel CG, et al. Among authors: striano p. Epilepsy Res. 2010 May;89(2-3):286-94. doi: 10.1016/j.eplepsyres.2010.01.013. Epub 2010 Feb 12. Epilepsy Res. 2010. PMID: 20153606

8

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

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

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.

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