Gambardella A - Search Results

1

Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy.

Bovo G, Diani E, Bisulli F, Di Bonaventura C, Striano P, Gambardella A, Ferlazzo E, Egeo G, Mecarelli O, Elia M, Bianchi A, Bortoluzzi S, Vettori A, Aguglia U, Binelli S, De Falco A, Coppola G, Gobbi G, Sofia V, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Bovo G, et al. Among authors: gambardella a. Neurosci Lett. 2008 May 2;436(1):23-6. doi: 10.1016/j.neulet.2008.02.045. Epub 2008 Mar 4. Neurosci Lett. 2008. PMID: 18355961

2

Sleep-induced masticatory myoclonus: a rare parasomnia associated with insomnia.

Aguglia U, Gambardella A, Quattrone A. Aguglia U, et al. Among authors: gambardella a. Sleep. 1991 Feb;14(1):80-2. doi: 10.1093/sleep/14.1.80. Sleep. 1991. PMID: 1811324

3

Functional integrity of benzodiazepine receptors of the geniculo-striate visual pathways in Creutzfeldt-Jakob disease. A pharmacological evoked potential study.

Aguglia U, Oliveri RL, Gambardella A, Quattrone A. Aguglia U, et al. Among authors: gambardella a. J Neurol. 1993 Jan;240(1):25-7. doi: 10.1007/BF00838442. J Neurol. 1993. PMID: 8380846

4

De novo epileptic confusional status in a patient with cobalamin deficiency.

Aguglia U, Gambardella A, Oliveri RL, De Sarro G, Zappia M, Quattrone A. Aguglia U, et al. Among authors: gambardella a. Metab Brain Dis. 1995 Sep;10(3):233-8. doi: 10.1007/BF02081028. Metab Brain Dis. 1995. PMID: 8830283

5

Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients.

Gambardella A, Aguglia U, Guerrini R, Morelli F, Zappia M, Quattrone A. Gambardella A, et al. Brain Dev. 1996 May-Jun;18(3):212-5. doi: 10.1016/0387-7604(95)00133-6. Brain Dev. 1996. PMID: 8836503

6

Spontaneous remission of childhood epilepsy in two patients with focal extraopercular cortical dysplasia.

Gambardella A, Le Piane E, Oliveri RL, Zappia M, Pardatscher K, Quattrone A, Aguglia U. Gambardella A, et al. Brain Dev. 1997 Sep;19(6):422-5. doi: 10.1016/s0387-7604(97)00047-8. Brain Dev. 1997. PMID: 9339872

7

Myoclonic absence-like seizures and chromosome abnormality syndromes.

Elia M, Guerrini R, Musumeci SA, Bonanni P, Gambardella A, Aguglia U. Elia M, et al. Among authors: gambardella a. Epilepsia. 1998 Jun;39(6):660-3. doi: 10.1111/j.1528-1157.1998.tb01435.x. Epilepsia. 1998. PMID: 9637609 Free article.

8

Mild non-lesional temporal lobe epilepsy. A common, unrecognized disorder with onset in adulthood.

Aguglia U, Gambardella A, Le Piane E, Messina D, Oliveri RL, Russo C, Zappia M, Quattrone A. Aguglia U, et al. Among authors: gambardella a. Can J Neurol Sci. 1998 Nov;25(4):282-6. doi: 10.1017/s0317167100034284. Can J Neurol Sci. 1998. PMID: 9827228

9

Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD.

Oliveri RL, Annesi G, Zappia M, Civitelli D, Montesanti R, Branca D, Nicoletti G, Spadafora P, Pasqua AA, Cittadella R, Andreoli V, Gambardella A, Aguglia U, Quattrone A. Oliveri RL, et al. Among authors: gambardella a. Neurology. 1999 Oct 22;53(7):1425-30. doi: 10.1212/wnl.53.7.1425. Neurology. 1999. PMID: 10534246

10

Apolipoprotein E polymorphisms and the risk of nonlesional temporal lobe epilepsy.

Gambardella A, Aguglia U, Cittadella R, Romeo N, Sibilia G, LePiane E, Messina D, Manna I, Oliveri RL, Zappia M, Quattrone A. Gambardella A, et al. Epilepsia. 1999 Dec;40(12):1804-7. doi: 10.1111/j.1528-1157.1999.tb01602.x. Epilepsia. 1999. PMID: 10612348 Free article.

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