Gambardella A - Search Results

1

SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure.

Dibbens LM, Michelucci R, Gambardella A, Andermann F, Rubboli G, Bayly MA, Joensuu T, Vears DF, Franceschetti S, Canafoglia L, Wallace R, Bassuk AG, Power DA, Tassinari CA, Andermann E, Lehesjoki AE, Berkovic SF. Dibbens LM, et al. Among authors: gambardella a. Ann Neurol. 2009 Oct;66(4):532-6. doi: 10.1002/ana.21765. Ann Neurol. 2009. PMID: 19847901

2

Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results.

Palmini A, Gambardella A, Andermann F, Dubeau F, da Costa JC, Olivier A, Tampieri D, Gloor P, Quesney F, Andermann E, et al. Palmini A, et al. Among authors: gambardella a. Ann Neurol. 1995 Apr;37(4):476-87. doi: 10.1002/ana.410370410. Ann Neurol. 1995. PMID: 7717684

3

The relation of spike foci and of clinical seizure characteristics to different patterns of mesial temporal atrophy.

Gambardella A, Gotman J, Cendes F, Andermann F. Gambardella A, et al. Arch Neurol. 1995 Mar;52(3):287-93. doi: 10.1001/archneur.1995.00540270083023. Arch Neurol. 1995. PMID: 7872883

4

Late-onset drop attacks in temporal lobe epilepsy: a reevaluation of the concept of temporal lobe syncope.

Gambardella A, Reutens DC, Andermann F, Cendes F, Gloor P, Dubeau F, Olivier A. Gambardella A, et al. Neurology. 1994 Jun;44(6):1074-8. doi: 10.1212/wnl.44.6.1074. Neurology. 1994. PMID: 8208403

5

Usefulness of focal rhythmic discharges on scalp EEG of patients with focal cortical dysplasia and intractable epilepsy.

Gambardella A, Palmini A, Andermann F, Dubeau F, Da Costa JC, Quesney LF, Andermann E, Olivier A. Gambardella A, et al. Electroencephalogr Clin Neurophysiol. 1996 Apr;98(4):243-9. doi: 10.1016/0013-4694(95)00266-9. Electroencephalogr Clin Neurophysiol. 1996. PMID: 8641147

6

A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy. A video-polygraphic study.

Capovilla G, Rubboli G, Beccaria F, Lorenzetti ME, Montagnini A, Resi C, Gardella E, Gambardella A, Romeo A, Tassinari CA. Capovilla G, et al. Among authors: gambardella a. Epileptic Disord. 2001 Jun;3(2):57-62. Epileptic Disord. 2001. PMID: 11431166 Free article.

7

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. Neurology. 2001 Aug 28;57(4):708-11. doi: 10.1212/wnl.57.4.708. Neurology. 2001. PMID: 11524486

8

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy.

Berkovic SF, Heron SE, Giordano L, Marini C, Guerrini R, Kaplan RE, Gambardella A, Steinlein OK, Grinton BE, Dean JT, Bordo L, Hodgson BL, Yamamoto T, Mulley JC, Zara F, Scheffer IE. Berkovic SF, et al. Among authors: gambardella a. Ann Neurol. 2004 Apr;55(4):550-7. doi: 10.1002/ana.20029. Ann Neurol. 2004. PMID: 15048894

9

Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy.

D'Agostino D, Bertelli M, Gallo S, Cecchin S, Albiero E, Garofalo PG, Gambardella A, St Hilaire JM, Kwiecinski H, Andermann E, Pandolfo M. D'Agostino D, et al. Among authors: gambardella a. Neurology. 2004 Oct 26;63(8):1500-2. doi: 10.1212/01.wnl.0000142093.94998.1a. Neurology. 2004. PMID: 15505175

10

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.

Striano P, Gambardella A, Coppola A, Di Bonaventura C, Bovo G, Diani E, Boaretto F, Egeo G, Ciampa C, Labate A, Testoni S, Passarelli D, Manna I, Sferro C, Aguglia U, Caranci F, Giallonardo AT, Striano S, Nobile C, Michelucci R. Striano P, et al. Among authors: gambardella a. J Neurol. 2008 Jan;255(1):16-23. doi: 10.1007/s00415-007-0653-1. Epub 2007 Nov 21. J Neurol. 2008. PMID: 18004642

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