-
1
-
-
0036210771
-
Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24
-
Brodtkorb E, Gu W, Nakken KO, Fischer C, Steinlein OK (2002) Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24. Epilepsia 43:228-235
-
(2002)
Epilepsia
, vol.43
, pp. 228-235
-
-
Brodtkorb, E.1
Gu, W.2
Nakken, K.O.3
Fischer, C.4
Steinlein, O.K.5
-
2
-
-
0037799473
-
Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features
-
Fertig E, Lincoln A, Martinuzzi A, Mattson RH, Hisama FM (2003) Novel LGI1 mutation in a family with autosomal dominant partial epilepsy with auditory features. Neurology 60: 1687-1690
-
(2003)
Neurology
, vol.60
, pp. 1687-1690
-
-
Fertig, E.1
Lincoln, A.2
Martinuzzi, A.3
Mattson, R.H.4
Hisama, F.M.5
-
3
-
-
0036712759
-
LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures
-
Gu W, Brodtkorb E, Steinlein OK (2002) LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures. Ann Neurol 52: 364-367
-
(2002)
Ann Neurol
, vol.52
, pp. 364-367
-
-
Gu, W.1
Brodtkorb, E.2
Steinlein, O.K.3
-
4
-
-
18544376557
-
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
-
Kalachikov S, Evgrafov O, Ross B, et al. (2002) Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet 30: 335-341
-
(2002)
Nat Genet
, vol.30
, pp. 335-341
-
-
Kalachikov, S.1
Evgrafov, O.2
Ross, B.3
-
5
-
-
0033869040
-
Autosomal dominant partial epilepsy with auditory features: Description of a new family
-
Michelucci R, Passarelli D, Pitzalis S, Dal Corso G, Tassinari CA, Nobile C (2000) Autosomal dominant partial epilepsy with auditory features: description of a new family. Epilepsia 41:967-970
-
(2000)
Epilepsia
, vol.41
, pp. 967-970
-
-
Michelucci, R.1
Passarelli, D.2
Pitzalis, S.3
Dal Corso, G.4
Tassinari, C.A.5
Nobile, C.6
-
6
-
-
18344363561
-
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
-
Morante-Redolat JM, Gorostidi-Pagola A, Piquier-Sirerol S, et al. (2002) Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet 11:1119-1128
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1119-1128
-
-
Morante-Redolat, J.M.1
Gorostidi-Pagola, A.2
Piquier-Sirerol, S.3
-
7
-
-
0029059069
-
Localization of a gene for partial epilepsy to chromosome 10q
-
Ottman R, Risch N, Hauser WA, et al. (1995) Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet 10:56-60
-
(1995)
Nat Genet
, vol.10
, pp. 56-60
-
-
Ottman, R.1
Risch, N.2
Hauser, W.A.3
-
8
-
-
0037371070
-
Epilepsy with auditory features: A LGI1 gene mutation suggests a loss-of-function mechanism
-
Pizzuti A, Flex E, Di Bonaventura C, Dottorini T, Egeo G, Manfredi M, Dallapiccola B, Giallonardo AT (2003) Epilepsy with auditory features: a LGI1 gene mutation suggests a loss-of-function mechanism. Ann Neurol 53: 396-399
-
(2003)
Ann Neurol
, vol.53
, pp. 396-399
-
-
Pizzuti, A.1
Flex, E.2
Di Bonaventura, C.3
Dottorini, T.4
Egeo, G.5
Manfredi, M.6
Dallapiccola, B.7
Giallonardo, A.T.8
-
9
-
-
0345003726
-
Autosomal dominant lateral temporal epilepsy: Clinical and genetic study of a large Basque pedigree linked to chromosome 10q
-
Poza JJ, Saenz A, Martinez-Gil A, et al. (1999) Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. Ann Neurol 45:182-188
-
(1999)
Ann Neurol
, vol.45
, pp. 182-188
-
-
Poza, J.J.1
Saenz, A.2
Martinez-Gil, A.3
-
10
-
-
0036192726
-
Four new families with autosomal dominant partial epilepsy with auditory features: Clinical description and linkage to chromosome 10q24
-
Winawer MR, Martinelli Boneschi F, Barker-Cummings C, et al. (2002) Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24. Epilepsia 43: 60-67
-
(2002)
Epilepsia
, vol.43
, pp. 60-67
-
-
Winawer, M.R.1
Martinelli Boneschi, F.2
Barker-Cummings, C.3
-
11
-
-
0034643891
-
Autosomal dominant partial epilepsy with auditory features: Defining the phenotype
-
Winawer MR, Ottman R, Hauser WA, Pedley TA (2000) Autosomal dominant partial epilepsy with auditory features: defining the phenotype. Neurology 54:2173-2176
-
(2000)
Neurology
, vol.54
, pp. 2173-2176
-
-
Winawer, M.R.1
Ottman, R.2
Hauser, W.A.3
Pedley, T.A.4
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