-
1
-
-
77950857874
-
Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009
-
Berg A.T., Berkovic S.F., Brodie M.J., Buchhalter J., Cross H., van Emde Boas W., Scheffer I.E. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009. Epilepsia 2010, 51(4):676-685.
-
(2010)
Epilepsia
, vol.51
, Issue.4
, pp. 676-685
-
-
Berg, A.T.1
Berkovic, S.F.2
Brodie, M.J.3
Buchhalter, J.4
Cross, H.5
van Emde Boas, W.6
Scheffer, I.E.7
-
2
-
-
11144355359
-
LGI1 mutations in temporal lobe epilepsies
-
Berkovic S.F., Izzillo P., McMahon J.M., Harkin L.A., McIntosh A.M., Phillips H.A., Mulley J.C. LGI1 mutations in temporal lobe epilepsies. Neurology 2004, 62(7):1115-1119.
-
(2004)
Neurology
, vol.62
, Issue.7
, pp. 1115-1119
-
-
Berkovic, S.F.1
Izzillo, P.2
McMahon, J.M.3
Harkin, L.A.4
McIntosh, A.M.5
Phillips, H.A.6
Mulley, J.C.7
-
3
-
-
2942588984
-
Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases
-
Bisulli F., Tinuper P., Avoni P., Striano P., Striano S., d'Orsi G., Michelucci R. Idiopathic partial epilepsy with auditory features (IPEAF): a clinical and genetic study of 53 sporadic cases. Brain 2004, 127(Pt 6):1343-1352.
-
(2004)
Brain
, vol.127
, Issue.PART 6
, pp. 1343-1352
-
-
Bisulli, F.1
Tinuper, P.2
Avoni, P.3
Striano, P.4
Striano, S.5
d'Orsi, G.6
Michelucci, R.7
-
4
-
-
34547812648
-
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy
-
Chabrol E., Gourfinkel-An I., Scheffer I.E., Picard F., Couarch P., Berkovic S.F., Baulac S. Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy. Epilepsy Research 2007, 76(1):41-48.
-
(2007)
Epilepsy Research
, vol.76
, Issue.1
, pp. 41-48
-
-
Chabrol, E.1
Gourfinkel-An, I.2
Scheffer, I.E.3
Picard, F.4
Couarch, P.5
Berkovic, S.F.6
Baulac, S.7
-
5
-
-
0023091631
-
Gustatory hallucinations in epileptic seizures, electrophysiological, clinical and anatomical correlates
-
Hausser-Hauw C., Bancaud J. Gustatory hallucinations in epileptic seizures, electrophysiological, clinical and anatomical correlates. Brain 1987, 110:339-359.
-
(1987)
Brain
, vol.110
, pp. 339-359
-
-
Hausser-Hauw, C.1
Bancaud, J.2
-
6
-
-
84858147236
-
Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF
-
Ho Y.-Y., Ionita-Laza I., Ottman R. Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF. Neurology 2012, 78(8):563-568.
-
(2012)
Neurology
, vol.78
, Issue.8
, pp. 563-568
-
-
Ho, Y.-Y.1
Ionita-Laza, I.2
Ottman, R.3
-
7
-
-
65549115991
-
Lateral temporal lobe epilepsies: clinical and genetic features
-
Michelucci R., Pasini E., Nobile C. Lateral temporal lobe epilepsies: clinical and genetic features. Epilepsia 2009, 50(5):52-54.
-
(2009)
Epilepsia
, vol.50
, Issue.5
, pp. 52-54
-
-
Michelucci, R.1
Pasini, E.2
Nobile, C.3
-
8
-
-
63749094521
-
LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy [Review]
-
Nobile C., Michelucci R., Andreazza S., Pasini E., Tosatto S.C.E., Striano P. LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy [Review]. Human Mutation 2009, 30(4):530-536.
-
(2009)
Human Mutation
, vol.30
, Issue.4
, pp. 530-536
-
-
Nobile, C.1
Michelucci, R.2
Andreazza, S.3
Pasini, E.4
Tosatto, S.C.E.5
Striano, P.6
-
9
-
-
0029059069
-
Localization of a gene for partial epilepsy to chromosome 10q
-
Ottman R., Risch N., Hauser W.A., Pedley T.A., Lee J.H., Barker-Cummings C., et al. Localization of a gene for partial epilepsy to chromosome 10q. Nature Genetics 1995, 10(1):56-60.
-
(1995)
Nature Genetics
, vol.10
, Issue.1
, pp. 56-60
-
-
Ottman, R.1
Risch, N.2
Hauser, W.A.3
Pedley, T.A.4
Lee, J.H.5
Barker-Cummings, C.6
-
10
-
-
1842580632
-
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
-
Ottman R., Winawer M.R., Kalachikov S., Barker-Cummings C., Gilliam T.C., Pedley T.A., Hauser W.A. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology 2004, 62(7):1120-1126.
-
(2004)
Neurology
, vol.62
, Issue.7
, pp. 1120-1126
-
-
Ottman, R.1
Winawer, M.R.2
Kalachikov, S.3
Barker-Cummings, C.4
Gilliam, T.C.5
Pedley, T.A.6
Hauser, W.A.7
-
11
-
-
64449088896
-
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
-
Scheffer I., Zhang Y., Jansen F., Dibbens L. Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?. Brain and Development 2009, 31:394-400.
-
(2009)
Brain and Development
, vol.31
, pp. 394-400
-
-
Scheffer, I.1
Zhang, Y.2
Jansen, F.3
Dibbens, L.4
-
12
-
-
34548132407
-
Multiple auras. Clinical significance and pahtophysiology
-
Widdess-Walsh P., Kotagal P., Jeha L., Wu G., Burgess R. Multiple auras. Clinical significance and pahtophysiology. Neurology 2007, 69:755-761.
-
(2007)
Neurology
, vol.69
, pp. 755-761
-
-
Widdess-Walsh, P.1
Kotagal, P.2
Jeha, L.3
Wu, G.4
Burgess, R.5
-
13
-
-
0036192726
-
Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24
-
Winawer M.R., Martinelli Boneschi F., Barker-Cummings C., Lee J.H., Liu J., Mekios C., Ottman R. Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24. Epilepsia 2002, 43(1):60-67.
-
(2002)
Epilepsia
, vol.43
, Issue.1
, pp. 60-67
-
-
Winawer, M.R.1
Martinelli Boneschi, F.2
Barker-Cummings, C.3
Lee, J.H.4
Liu, J.5
Mekios, C.6
Ottman, R.7
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