-
2
-
-
0029834204
-
Familial temporal lobe epilepsy: A common disorder identified in twins
-
Berkovic SF, McIntosh A, Howell RA, et al. Familial temporal lobe epilepsy: a common disorder identified in twins. Ann Neurol 1996;40:227-235.
-
(1996)
Ann Neurol
, vol.40
, pp. 227-235
-
-
Berkovic, S.F.1
McIntosh, A.2
Howell, R.A.3
-
3
-
-
0031911013
-
Familial temporal lobe epilepsy: A clinically heterogeneous syndrome
-
Cendes F, Lopes-Cendes I, Andermann E, Andermann F. Familial temporal lobe epilepsy: a clinically heterogeneous syndrome. Neurology 1998;50:554-557.
-
(1998)
Neurology
, vol.50
, pp. 554-557
-
-
Cendes, F.1
Lopes-Cendes, I.2
Andermann, E.3
Andermann, F.4
-
4
-
-
33644802824
-
Genetic focal epilepsies: State of the art and paths to the future
-
Andermann F, Kobayashi E, Andermann E. Genetic focal epilepsies: state of the art and paths to the future. Epilepsia 2005;46(suppl 10):61-67.
-
(2005)
Epilepsia
, vol.46
, Issue.SUPPL. 10
, pp. 61-67
-
-
Andermann, F.1
Kobayashi, E.2
Andermann, E.3
-
5
-
-
18544376557
-
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
-
Kalachikov S, Evgrafov O, Ross B, et al. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet 2002;30:335-341.
-
(2002)
Nat Genet
, vol.30
, pp. 335-341
-
-
Kalachikov, S.1
Evgrafov, O.2
Ross, B.3
-
6
-
-
18344363561
-
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
-
Morante-Redolat JM, Gorostidi-Pagola A, Piquer-Sirerol S, et al. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet 2002;11:1119-1128.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1119-1128
-
-
Morante-Redolat, J.M.1
Gorostidi-Pagola, A.2
Piquer-Sirerol, S.3
-
7
-
-
1842580632
-
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
-
Ottman R, Winawer MR, Kalachikov S, et al. LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology 2004;62:1120-1126.
-
(2004)
Neurology
, vol.62
, pp. 1120-1126
-
-
Ottman, R.1
Winawer, M.R.2
Kalachikov, S.3
-
8
-
-
1542409182
-
Autosomal dominant lateral temporal epilepsy: Two families with novel mutations in the LGI1 gene
-
Hedera P, Abou-Khalil B, Crunk EM, et al. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene. Epilepsia 2004;45:218-222.
-
(2004)
Epilepsia
, vol.45
, pp. 218-222
-
-
Hedera, P.1
Abou-Khalil, B.2
Crunk, E.M.3
-
9
-
-
0034985911
-
Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31
-
Baulac S, Picard F, Herman A, et al. Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31. Ann Neurol 2001;49:786-792.
-
(2001)
Ann Neurol
, vol.49
, pp. 786-792
-
-
Baulac, S.1
Picard, F.2
Herman, A.3
-
10
-
-
4444324827
-
Novel locus on chromosome 12q22-q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures
-
Claes L, Audenaert D, Deprez L, et al. Novel locus on chromosome 12q22-q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures. J Med Genet 2004;41:710-714.
-
(2004)
J Med Genet
, vol.41
, pp. 710-714
-
-
Claes, L.1
Audenaert, D.2
Deprez, L.3
-
11
-
-
0024317220
-
Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy
-
Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy. Epilepsia 1989;30:389-399.
-
(1989)
Epilepsia
, vol.30
, pp. 389-399
-
-
-
12
-
-
0021850103
-
Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
-
Lathrop GM, Lalouel JM, Julier C, Ott J. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 1985;37:482-498.
-
(1985)
Am J Hum Genet
, vol.37
, pp. 482-498
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
13
-
-
0035793026
-
Sodium-hydrogen exchangers and sodium-bicarbonate co-transporters: Ontogeny of protein expression in the rat brain
-
Douglas RM, Schmitt BM, Xia Y, et al. Sodium-hydrogen exchangers and sodium-bicarbonate co-transporters: ontogeny of protein expression in the rat brain. Neuroscience 2001;102:217-228.
-
(2001)
Neuroscience
, vol.102
, pp. 217-228
-
-
Douglas, R.M.1
Schmitt, B.M.2
Xia, Y.3
-
14
-
-
0042238048
-
The evidence for GABAB receptor-mediated regulation of acid-base balance: Involvement of Na+/H+ exchanger and Na+/HCO3-cotransporter
-
Kang TC, An SJ, Park SK, Hwang IK, Bae JC, Won MH. The evidence for GABAB receptor-mediated regulation of acid-base balance: involvement of Na+/H+ exchanger and Na+/HCO3-cotransporter. Brain Res Mol Brain Res 2003;114:86-90.
-
(2003)
Brain Res Mol Brain Res
, vol.114
, pp. 86-90
-
-
Kang, T.C.1
An, S.J.2
Park, S.K.3
Hwang, I.K.4
Bae, J.C.5
Won, M.H.6
-
15
-
-
0028844053
-
Cyclin I: A new cyclin encoded by a gene isolated from human brain
-
Nakamura T, Sanokawa R, Sasaki YF, et al. Cyclin I: a new cyclin encoded by a gene isolated from human brain. Exp Cell Res 1995;221:534-542.
-
(1995)
Exp Cell Res
, vol.221
, pp. 534-542
-
-
Nakamura, T.1
Sanokawa, R.2
Sasaki, Y.F.3
-
16
-
-
0037178863
-
Cyclin G2 associates with protein phosphatase 2A catalytic and regulatory B' subunits in active complexes and induces nuclear aberrations and a G1/S phase cell cycle arrest
-
Bennin DA, Don AS, Brake T, et al. Cyclin G2 associates with protein phosphatase 2A catalytic and regulatory B' subunits in active complexes and induces nuclear aberrations and a G1/S phase cell cycle arrest. J Biol Chem 2002;277:27449-27467.
-
(2002)
J Biol Chem
, vol.277
, pp. 27449-27467
-
-
Bennin, D.A.1
Don, A.S.2
Brake, T.3
-
17
-
-
0019942526
-
Epidemiology of seizure disorders in children
-
Leviton A, Cowan LD. Epidemiology of seizure disorders in children. Neuroepidemiology 1982;1:40-83.
-
(1982)
Neuroepidemiology
, vol.1
, pp. 40-83
-
-
Leviton, A.1
Cowan, L.D.2
-
19
-
-
85030524057
-
A new locus for familial temporal lobe epilepsy
-
Pandolfo M, Chahine L, Abou-Khalil B, et al. A new locus for familial temporal lobe epilepsy. Neurology 2006;66(suppl 2):A138.
-
(2006)
Neurology
, vol.66
, Issue.SUPPL. 2
-
-
Pandolfo, M.1
Chahine, L.2
Abou-Khalil, B.3
|