Ventura P - Search Results

1

ApoE epsilon4 allele and disease duration affect verbal learning in mild temporal lobe epilepsy.

Gambardella A, Aguglia U, Chifari R, Labate A, Manna I, Serra P, Romeo N, Sibilia G, Lepiane E, Russa AL, Ventura P, Cittadella R, Sasanelli F, Colosimo E, Leggio U, Zappia M, Quattrone A. Gambardella A, et al. Among authors: ventura p. Epilepsia. 2005 Jan;46(1):110-7. doi: 10.1111/j.0013-9580.2005.15804.x. Epilepsia. 2005. PMID: 15660776 Free article.

2

MRI evidence of mesial temporal sclerosis in sporadic "benign" temporal lobe epilepsy.

Labate A, Ventura P, Gambardella A, Le Piane E, Colosimo E, Leggio U, Ambrosio R, Condino F, Messina D, Lanza P, Aguglia U, Quattrone A. Labate A, et al. Among authors: ventura p. Neurology. 2006 Feb 28;66(4):562-5. doi: 10.1212/01.wnl.0000198208.59347.96. Neurology. 2006. PMID: 16505312

3

Temporal lobe abnormalities on brain MRI in healthy volunteers: a prospective case-control study.

Labate A, Gambardella A, Aguglia U, Condino F, Ventura P, Lanza P, Quattrone A. Labate A, et al. Among authors: ventura p. Neurology. 2010 Feb 16;74(7):553-7. doi: 10.1212/WNL.0b013e3181cff747. Epub 2010 Jan 20. Neurology. 2010. PMID: 20089943

4

Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.

Annesi G, Gambardella A, Carrideo S, Incorpora G, Labate A, Pasqua AA, Civitelli D, Polizzi A, Annesi F, Spadafora P, Tarantino P, Cirò Candiano IC, Romeo N, De Marco EV, Ventura P, LePiane E, Zappia M, Aguglia U, Pavone L, Quattrone A. Annesi G, et al. Among authors: ventura p. Epilepsia. 2003 Sep;44(9):1257-8. doi: 10.1046/j.1528-1157.2003.22503.x. Epilepsia. 2003. PMID: 12919402 Free article. No abstract available.

5

Familial paroxysmal exercise-induced dyskinesia, epilepsy, and mental retardation in a family with autosomal dominant inheritance.

Perniola T, Margari L, de Iaco MG, Presicci A, Ventura P, Ferrannini E, Illiceto G. Perniola T, et al. Among authors: ventura p. Mov Disord. 2001 Jul;16(4):724-30. doi: 10.1002/mds.1117. Mov Disord. 2001. PMID: 11481699

6

Clinical and instrumental (magnetic resonance imaging [MRI] and multimodal evoked potentials) follow-up of brain lesions in three young patients with neurofibromatosis 1.

Margari L, Presicci A, Ventura P, Maria Bacca S, Iliceto G, Medicamento N, Buttiglione M, Perniola T. Margari L, et al. Among authors: ventura p. J Child Neurol. 2006 Dec;21(12):1085-90. doi: 10.1177/7010.2006.00124. J Child Neurol. 2006. PMID: 17156707

7

Megalocornea and mental retardation syndrome: clinical and instrumental follow-up of a case.

Margari L, Presicci A, Ventura P, Buttiglione M, Dicuonzo F, Lattarulo C, Perniola T. Margari L, et al. Among authors: ventura p. J Child Neurol. 2006 Oct;21(10):893-6. doi: 10.1177/08830738060210100801. J Child Neurol. 2006. PMID: 17005108

8

A novel familial MECP2 mutation in a young boy: clinical and molecular findings.

Ventura P, Galluzzi R, Bacca SM, Giorda R, Massagli A. Ventura P, et al. Neurology. 2006 Sep 12;67(5):867-8. doi: 10.1212/01.wnl.0000233990.87889.15. Neurology. 2006. PMID: 16966553

9

Congenital ataxia and mental retardation in three brothers.

Margari L, Ventura P, Presicci A, Buttiglione M, Perniola T. Margari L, et al. Among authors: ventura p. Pediatr Neurol. 2004 Jul;31(1):59-63. doi: 10.1016/j.pediatrneurol.2004.01.006. Pediatr Neurol. 2004. PMID: 15246495

10

Brain magnetic resonance spectroscopy in Sydenham's chorea and ADHD.

Margari L, Ventura P, Portoghese C, Presicci A, Buttiglione M, Di Cuonzo F. Margari L, et al. Among authors: ventura p. Pediatr Neurol. 2006 Jun;34(6):467-73. doi: 10.1016/j.pediatrneurol.2005.10.014. Pediatr Neurol. 2006. PMID: 16765826

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