Oliveri RL - Search Results

1

Familial temporal lobe epilepsy autosomal dominant inheritance in a large pedigree from southern Italy.

Gambardella A, Messina D, Le Piane E, Oliveri RL, Annesi G, Zappia M, Andermann E, Quattrone A, Aguglia U. Gambardella A, et al. Among authors: oliveri rl. Epilepsy Res. 2000 Feb;38(2-3):127-32. doi: 10.1016/s0920-1211(99)00080-7. Epilepsy Res. 2000. PMID: 10642040

2

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: oliveri rl. Can J Neurol Sci. 1998 Nov;25(4):282-6. doi: 10.1017/s0317167100034284. Can J Neurol Sci. 1998. PMID: 9827228

3

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. Among authors: oliveri rl. Epilepsia. 1999 Dec;40(12):1804-7. doi: 10.1111/j.1528-1157.1999.tb01602.x. Epilepsia. 1999. PMID: 10612348 Free article.

4

Interhemispheric threshold differences in idiopathic generalized epilepsies with versive or circling seizures determined with focal magnetic transcranial stimulation.

Aguglia U, Gambardella A, Quartarone A, Girlanda P, Le Piane E, Messina D, Oliveri RL, Zappia M, Quattrone A. Aguglia U, et al. Among authors: oliveri rl. Epilepsy Res. 2000 Jun;40(1):1-6. doi: 10.1016/s0920-1211(99)00105-9. Epilepsy Res. 2000. PMID: 10771252

5

A new locus for autosomal dominant nocturnal frontal lobe epilepsy maps to chromosome 1.

Gambardella A, Annesi G, De Fusco M, Patrignani A, Aguglia U, Annesi F, Pasqua AA, Spadafora P, Oliveri RL, Valentino P, Zappia M, Ballabio A, Casari G, Quattrone A. Gambardella A, et al. Among authors: oliveri rl. Neurology. 2000 Nov 28;55(10):1467-71. doi: 10.1212/wnl.55.10.1467. Neurology. 2000. PMID: 11094099

6

Photic-induced epileptic negative myoclonus: a case report.

Gambardella A, Aguglia U, Oliveri RL, Pucci F, Zappia M, Quattrone A. Gambardella A, et al. Among authors: oliveri rl. Epilepsia. 1996 May;37(5):492-4. doi: 10.1111/j.1528-1157.1996.tb00596.x. Epilepsia. 1996. PMID: 8617179

7

Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.

Quattrone A, Gambardella A, Bono F, Aguglia U, Bolino A, Bruni AC, Montesi MP, Oliveri RL, Sabatelli M, Tamburrini O, Valentino P, Van Broeckhoven C, Zappia M. Quattrone A, et al. Among authors: oliveri rl. Neurology. 1996 May;46(5):1318-24. doi: 10.1212/wnl.46.5.1318. Neurology. 1996. PMID: 8628474

8

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: oliveri rl. Metab Brain Dis. 1995 Sep;10(3):233-8. doi: 10.1007/BF02081028. Metab Brain Dis. 1995. PMID: 8830283

9

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. Among authors: oliveri rl. Brain Dev. 1997 Sep;19(6):422-5. doi: 10.1016/s0387-7604(97)00047-8. Brain Dev. 1997. PMID: 9339872

10

Negative myoclonic status due to antiepileptic drug tapering: report of three cases.

Gambardella A, Aguglia U, Oliveri RL, Russo C, Zappia M, Quattrone A. Gambardella A, et al. Among authors: oliveri rl. Epilepsia. 1997 Jul;38(7):819-23. doi: 10.1111/j.1528-1157.1997.tb01469.x. Epilepsia. 1997. PMID: 9579909 Free article.

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