Labate A - Search Results

1

Brivaracetam use in clinical practice: a Delphi consensus on its role as first add-on therapy in focal epilepsy and beyond.

Lattanzi S, Chiesa V, Di Gennaro G, Ferlazzo E, Labate A, La Neve A, Meletti S, Di Bonaventura C; Consensus Collaborators Group. Lattanzi S, et al. Among authors: labate a. Neurol Sci. 2024 Sep;45(9):4519-4527. doi: 10.1007/s10072-024-07485-w. Epub 2024 Apr 1. Neurol Sci. 2024. PMID: 38558319 Free PMC article.

2

A functional genetic variation of the 5-HTR2A receptor affects age at onset in patients with temporal lobe epilepsy.

Manna I, Labate A, Mumoli L, Palamara G, Ferlazzo E, Aguglia U, Quattrone A, Gambardella A. Manna I, et al. Among authors: labate a. Ann Hum Genet. 2012 Jul;76(4):277-82. doi: 10.1111/j.1469-1809.2012.00713.x. Ann Hum Genet. 2012. PMID: 22681516

3

Teaching neuroimages: Pseudohypertrophic cerebral cortex in end-stage Creutzfeldt-Jakob disease.

Gasparini S, Ferlazzo E, Branca D, Labate A, Cianci V, Latella MA, Aguglia U. Gasparini S, et al. Among authors: labate a. Neurology. 2013 Jan 8;80(2):e21. doi: 10.1212/WNL.0b013e31827b92bd. Neurology. 2013. PMID: 23296137

4

Mutations in PRRT2 result in familial infantile seizures with heterogeneous phenotypes including febrile convulsions and probable SUDEP.

Labate A, Tarantino P, Palamara G, Gagliardi M, Cavalcanti F, Ferlazzo E, Sturniolo M, Incorpora G, Annesi G, Aguglia U, Gambardella A. Labate A, et al. Epilepsy Res. 2013 May;104(3):280-4. doi: 10.1016/j.eplepsyres.2012.10.014. Epub 2013 Jan 23. Epilepsy Res. 2013. PMID: 23352743

5

Failure to confirm association of a polymorphism in KCNMB4 gene with mesial temporal lobe epilepsy.

Manna I, Labate A, Mumoli L, Ferlazzo E, Aguglia U, Quattrone A, Gambardella A. Manna I, et al. Among authors: labate a. Epilepsy Res. 2013 Sep;106(1-2):284-7. doi: 10.1016/j.eplepsyres.2013.03.014. Epub 2013 Apr 25. Epilepsy Res. 2013. PMID: 23623847

6

No evidence for a role of the coding variant of the Toll-like receptor 4 gene in temporal lobe epilepsy.

Manna I, Labate A, Mumoli L, Ferlazzo E, Aguglia U, Quattrone A, Gambardella A. Manna I, et al. Among authors: labate a. Seizure. 2013 Nov;22(9):791-3. doi: 10.1016/j.seizure.2013.05.012. Epub 2013 Jun 27. Seizure. 2013. PMID: 23810712 Free article.

7

Permutation entropy of scalp EEG: a tool to investigate epilepsies: suggestions from absence epilepsies.

Ferlazzo E, Mammone N, Cianci V, Gasparini S, Gambardella A, Labate A, Latella MA, Sofia V, Elia M, Morabito FC, Aguglia U. Ferlazzo E, et al. Among authors: labate a. Clin Neurophysiol. 2014 Jan;125(1):13-20. doi: 10.1016/j.clinph.2013.06.023. Epub 2013 Jul 13. Clin Neurophysiol. 2014. PMID: 23859939

8

Detection of hippocampal atrophy in patients with temporal lobe epilepsy: a 3-Tesla MRI shape.

Mumoli L, Labate A, Vasta R, Cherubini A, Ferlazzo E, Aguglia U, Quattrone A, Gambardella A. Mumoli L, et al. Among authors: labate a. Epilepsy Behav. 2013 Sep;28(3):489-93. doi: 10.1016/j.yebeh.2013.05.035. Epub 2013 Jul 25. Epilepsy Behav. 2013. PMID: 23892579

9

Family history and frontal lobe seizures predict long-term remission in newly diagnosed cryptogenic focal epilepsy.

Gasparini S, Ferlazzo E, Beghi E, Tripepi G, Labate A, Mumoli L, Leonardi CG, Cianci V, Latella MA, Gambardella A, Aguglia U. Gasparini S, et al. Among authors: labate a. Epilepsy Res. 2013 Nov;107(1-2):101-8. doi: 10.1016/j.eplepsyres.2013.07.004. Epub 2013 Aug 5. Epilepsy Res. 2013. PMID: 23968820

10

Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene.

Manna I, Mumoli L, Labate A, Citrigno L, Ferlazzo E, Aguglia U, Quattrone A, Gambardella A. Manna I, et al. Among authors: labate a. Epilepsy Res. 2014 Mar;108(3):597-9. doi: 10.1016/j.eplepsyres.2013.11.011. Epub 2013 Nov 18. Epilepsy Res. 2014. PMID: 24315022

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