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281 results

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Validation Study of Italian Version of Inventory for Déjà Vu Experiences Assessment (I-IDEA): A Screening Tool to Detect Déjà Vu Phenomenon in Italian Healthy Individuals.
Mumoli L, Tripepi G, Aguglia U, Augimeri A, Baggetta R, Bisulli F, Bruni A, Cavalli SM, D'Aniello A, Daniele O, Di Bonaventura C, Di Gennaro G, Fattouch J, Ferlazzo E, Ferrari A, Giallonardo A, Gasparini S, Nigro S, Romigi A, Sofia V, Tinuper P, Vaccaro MG, Zummo L, Quattrone A, Gambardella A, Labate A. Mumoli L, et al. Among authors: labate a. Behav Sci (Basel). 2017 Aug 7;7(3):50. doi: 10.3390/bs7030050. Behav Sci (Basel). 2017. PMID: 28783090 Free PMC article.
The parkin gene is not involved in late-onset Parkinson's disease.
Oliveri RL, Zappia M, Annesi G, Bosco D, Annesi F, Spadafora P, Pasqua AA, Tomaino C, Nicoletti G, Pirritano D, Labate A, Gambardella A, Logroscino G, Manobianca G, Epifanio A, Morgante L, Savettieri G, Quattrone A. Oliveri RL, et al. Among authors: labate a. Neurology. 2001 Jul 24;57(2):359-62. doi: 10.1212/wnl.57.2.359. Neurology. 2001. PMID: 11468333
Juvenile Huntington's disease presenting as progressive myoclonic epilepsy.
Gambardella A, Muglia M, Labate A, Magariello A, Gabriele AL, Mazzei R, Pirritano D, Conforti FL, Patitucci A, Valentino P, Zappia M, Quattrone A. Gambardella A, et al. Among authors: labate a. Neurology. 2001 Aug 28;57(4):708-11. doi: 10.1212/wnl.57.4.708. Neurology. 2001. PMID: 11524486
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings.
Oliveri RL, Muglia M, De Stefano N, Mazzei R, Labate A, Conforti FL, Patitucci A, Gabriele AL, Tagarelli G, Magariello A, Zappia M, Gambardella A, Federico A, Quattrone A. Oliveri RL, et al. Among authors: labate a. Arch Neurol. 2001 Sep;58(9):1418-22. doi: 10.1001/archneur.58.9.1418. Arch Neurol. 2001. PMID: 11559313
Silent celiac disease in patients with childhood localization-related epilepsies.
Labate A, Gambardella A, Messina D, Tammaro S, Le Piane E, Pirritano D, Cosco C, Doldo P, Mazzei R, Oliveri RL, Bosco D, Zappia M, Valentino P, Aguglia U, Quattrone A. Labate A, et al. Epilepsia. 2001 Sep;42(9):1153-5. doi: 10.1046/j.1528-1157.2001.45700.x. Epilepsia. 2001. PMID: 11580763 Free article.
GABA(B) receptor 1 polymorphism (G1465A) is associated with temporal lobe epilepsy.
Gambardella A, Manna I, Labate A, Chifari R, La Russa A, Serra P, Cittadella R, Bonavita S, Andreoli V, LePiane E, Sasanelli F, Di Costanzo A, Zappia M, Tedeschi G, Aguglia U, Quattrone A. Gambardella A, et al. Among authors: labate a. Neurology. 2003 Feb 25;60(4):560-3. doi: 10.1212/01.wnl.0000046520.79877.d8. Neurology. 2003. PMID: 12601092
Prodynorphin gene promoter polymorphism and temporal lobe epilepsy.
Gambardella A, Manna I, Labate A, Chifari R, Serra P, La Russa A, LePiane E, Cittadella R, Andreoli V, Sasanelli F, Zappia M, Aguglia U, Quattrone A. Gambardella A, et al. Among authors: labate a. Epilepsia. 2003 Sep;44(9):1255-6. doi: 10.1046/j.1528-1157.2003.18003.x. Epilepsia. 2003. PMID: 12919401 Free article. No abstract available.
Temporal lobe epilepsy as a unique manifestation of multiple sclerosis.
Gambardella A, Valentino P, Labate A, Sibilia G, Ruscica F, Colosimo E, Nisticò R, Messina D, Zappia M, Quattrone A. Gambardella A, et al. Among authors: labate a. Can J Neurol Sci. 2003 Aug;30(3):228-32. doi: 10.1017/s031716710000264x. Can J Neurol Sci. 2003. PMID: 12945947
Startle epilepsy complicating aspartylglucosaminuria.
Labate A, Barone R, Gambardella A, Civitelli D, Fiumara A, Annesi G, Zappia M, Pavone L, Quattrone A. Labate A, et al. Brain Dev. 2004 Mar;26(2):130-3. doi: 10.1016/S0387-7604(03)00069-X. Brain Dev. 2004. PMID: 15036433
281 results