Santulli L - 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: santulli l. 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

A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms.

Coppola A, Striano P, Gimelli S, Ciampa C, Santulli L, Caranci F, Zuffardi O, Gimelli G, Striano S, Zara F. Coppola A, et al. Among authors: santulli l. Brain Dev. 2010 Mar;32(3):248-52. doi: 10.1016/j.braindev.2009.01.003. Epub 2009 Feb 11. Brain Dev. 2010. PMID: 19216040

3

Different electroclinical picture of generalized epilepsy in two families with 15q13.3 microdeletion.

Coppola A, Bagnasco I, Traverso M, Brusco A, Di Gregorio E, Del Gaudio L, Santulli L, Caccavale C, Vigliano P, Minetti C, Striano S, Zara F, Striano P. Coppola A, et al. Among authors: santulli l. Epilepsia. 2013 May;54(5):e69-73. doi: 10.1111/epi.12130. Epub 2013 Feb 28. Epilepsia. 2013. PMID: 23448223 Free article.

4

Natural history and long-term evolution in families with autosomal dominant cortical tremor, myoclonus, and epilepsy.

Coppola A, Santulli L, Del Gaudio L, Minetti C, Striano S, Zara F, Striano P. Coppola A, et al. Among authors: santulli l. Epilepsia. 2011 Jul;52(7):1245-50. doi: 10.1111/j.1528-1167.2011.03017.x. Epub 2011 Mar 22. Epilepsia. 2011. PMID: 21426326 Free article.

5

Neurological features and long-term follow-up in 15q11.2-13.1 duplication.

Coppola A, Ruosi P, Santulli L, Striano S, Zara F, Striano P, Sisodiya SM. Coppola A, et al. Among authors: santulli l. Eur J Med Genet. 2013 Nov;56(11):614-8. doi: 10.1016/j.ejmg.2013.08.008. Epub 2013 Sep 25. Eur J Med Genet. 2013. PMID: 24075935

6

The challenges of treating epilepsy with 25 antiepileptic drugs.

Santulli L, Coppola A, Balestrini S, Striano S. Santulli L, et al. Pharmacol Res. 2016 May;107:211-219. doi: 10.1016/j.phrs.2016.03.016. Epub 2016 Mar 16. Pharmacol Res. 2016. PMID: 26995307 Review.

7

Psychiatric comorbidities in patients from seven families with autosomal dominant cortical tremor, myoclonus, and epilepsy.

Coppola A, Caccavale C, Santulli L, Balestrini S, Cagnetti C, Licchetta L, Esposito M, Bisulli F, Tinuper P, Provinciali L, Minetti C, Zara F, Striano P, Striano S. Coppola A, et al. Among authors: santulli l. Epilepsy Behav. 2016 Mar;56:38-43. doi: 10.1016/j.yebeh.2015.12.038. Epub 2016 Jan 29. Epilepsy Behav. 2016. PMID: 26827300

8

Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases.

von Stülpnagel C, Hartlieb T, Borggräfe I, Coppola A, Gennaro E, Eschermann K, Kiwull L, Kluger F, Krois I, Møller RS, Rössler F, Santulli L, Schwermer C, Wallacher-Scholz B, Zara F, Wolf P, Kluger G. von Stülpnagel C, et al. Among authors: santulli l. Seizure. 2019 Feb;65:131-137. doi: 10.1016/j.seizure.2018.12.020. Epub 2018 Dec 22. Seizure. 2019. PMID: 30685520 Free article. Review.

9

The gelastic seizures-hypothalamic hamartoma syndrome: facts, hypotheses, and perspectives.

Striano S, Santulli L, Ianniciello M, Ferretti M, Romanelli P, Striano P. Striano S, et al. Among authors: santulli l. Epilepsy Behav. 2012 May;24(1):7-13. doi: 10.1016/j.yebeh.2012.02.013. Epub 2012 Apr 11. Epilepsy Behav. 2012. PMID: 22503469 Review.

10

Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual auras.

Dazzo E, Santulli L, Posar A, Fattouch J, Conti S, Lodén-van Straaten M, Mijalkovic J, De Bortoli M, Rosa M, Millino C, Pacchioni B, Di Bonaventura C, Giallonardo AT, Striano S, Striano P, Parmeggiani A, Nobile C. Dazzo E, et al. Among authors: santulli l. Epilepsy Res. 2015 Feb;110:132-8. doi: 10.1016/j.eplepsyres.2014.12.004. Epub 2014 Dec 16. Epilepsy Res. 2015. PMID: 25616465

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

18 results

Search Page