-
1
-
-
12144288765
-
Terminology and classification of the cortical dysplasias
-
Palmini A, Najm I, Babb T, Guerrini R, Foldvary-Schaefer N, Jackson G, et al. Terminology and classification of the cortical dysplasias. Neurology (2004) 62:S2-8. doi: 10.1212/01.WNL.0000114507.30388.7E
-
(2004)
Neurology
, vol.62
, pp. S2-S8
-
-
Palmini, A.1
Najm, I.2
Babb, T.3
Guerrini, R.4
Foldvary-Schaefer, N.5
Jackson, G.6
-
2
-
-
84921635928
-
High-throughput, automated quantification of white matter neurons in mild malformation of cortical development in epilepsy
-
Liu J, Ellis M, Brooke-Ball H, de Tisis J, Eriksson S, Brandner S, et al. High-throughput, automated quantification of white matter neurons in mild malformation of cortical development in epilepsy. Acta Neuropathol Commun (2014) 2:72. doi:10.1186/2051-5960-2-72
-
(2014)
Acta Neuropathol Commun
, vol.2
, pp. 72
-
-
Liu, J.1
Ellis, M.2
Brooke-Ball, H.3
de Tisis, J.4
Eriksson, S.5
Brandner, S.6
-
3
-
-
84879793001
-
International consensus classification of hippocampal sclerosis in temporal lobe epilepsy; a task force report from the ILEA commision on diagnostic methods
-
Blümcke I, Thom MJ, Aronica E, Armstrong D, Bartolomei F, Bernasconi A, et al. International consensus classification of hippocampal sclerosis in temporal lobe epilepsy; a task force report from the ILEA commision on diagnostic methods. Epilepsia (2013) 54:1315-29. doi:10.1111/epi.12220
-
(2013)
Epilepsia
, vol.54
, pp. 1315-1329
-
-
Blümcke, I.1
Thom, M.J.2
Aronica, E.3
Armstrong, D.4
Bartolomei, F.5
Bernasconi, A.6
-
4
-
-
0032536030
-
A potassium channel mutation in neonatal human epilepsy
-
Biervert C, Schroeder BC, Kubisch C, Berkovic S, Propping P, Jentsch J, et al. A potassium channel mutation in neonatal human epilepsy. Science (1998) 279:403-6. doi:10.1126/science.279.5349.403
-
(1998)
Science
, vol.279
, pp. 403-406
-
-
Biervert, C.1
Schroeder, B.C.2
Kubisch, C.3
Berkovic, S.4
Propping, P.5
Jentsch, J.6
-
5
-
-
0028077462
-
Classification of familial neonatal convulsions
-
Wakai S, Kamasaki H, Itoh N, Sueoka H, Kawamoto Y, Hayasaka H, et al. Classification of familial neonatal convulsions. Lancet (1994) 344:1376. doi:10.1016/S0140-6736(94)90742-0
-
(1994)
Lancet
, vol.344
, pp. 1376
-
-
Wakai, S.1
Kamasaki, H.2
Itoh, N.3
Sueoka, H.4
Kawamoto, Y.5
Hayasaka, H.6
-
6
-
-
33847216238
-
Benign familial neonatal convulsions: always benign?
-
Steinlein O, Conrad C, Weidner B. Benign familial neonatal convulsions: always benign? Epilepsy Res (2007) 73:245-9. doi:10.1016/j.eplepsyres.2006.10.010
-
(2007)
Epilepsy Res
, vol.73
, pp. 245-249
-
-
Steinlein, O.1
Conrad, C.2
Weidner, B.3
-
7
-
-
0344012023
-
KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum
-
Singh NA, Westenskow P, Charlier C, Pappas C, Leslie J, Dillon J, et al. KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum. Brain (2003) 126:2726-37. doi:10.1093/brain/awg286
-
(2003)
Brain
, vol.126
, pp. 2726-2737
-
-
Singh, N.A.1
Westenskow, P.2
Charlier, C.3
Pappas, C.4
Leslie, J.5
Dillon, J.6
-
8
-
-
84879757310
-
Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation
-
Kato M, Yamagat T, Kubota M, Arai H, Yamashita S, Nakagawa T, et al. Clinical spectrum of early onset epileptic encephalopathies caused by KCNQ2 mutation. Epilepsia (2013) 54:1282-7. doi:10.1111/epi.12200
-
(2013)
Epilepsia
, vol.54
, pp. 1282-1287
-
-
Kato, M.1
Yamagat, T.2
Kubota, M.3
Arai, H.4
Yamashita, S.5
Nakagawa, T.6
-
9
-
-
3242701298
-
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation
-
Borgatti R, Zucca C, Cavallin A, Ferrario M, Panzeri C, Castaldo P, et al. A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation. Neurology (2004) 63(1):57-65. doi:10.1212/01.WNL.0000132979.08394.6D
-
(2004)
Neurology
, vol.63
, Issue.1
, pp. 57-65
-
-
Borgatti, R.1
Zucca, C.2
Cavallin, A.3
Ferrario, M.4
Panzeri, C.5
Castaldo, P.6
-
10
-
-
0038059165
-
Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2
-
Dedek K, Fusco L, Teloy N, Steinlein O. Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2. Epilepsy Res (2003) 54:21-7. doi:10.1016/S0920-1211(03)00037-8
-
(2003)
Epilepsy Res
, vol.54
, pp. 21-27
-
-
Dedek, K.1
Fusco, L.2
Teloy, N.3
Steinlein, O.4
-
11
-
-
23944521562
-
Neonatal seizures with tonic clonic sequences and poor developmental outcome
-
Schmitt B, Wohlrab G, Sander T, Steinlein O, Hajnal B. Neonatal seizures with tonic clonic sequences and poor developmental outcome. Epilepsy Res (2005) 65:161-8. doi:10.1016/j.eplepsyres.2005.05.009
-
(2005)
Epilepsy Res
, vol.65
, pp. 161-168
-
-
Schmitt, B.1
Wohlrab, G.2
Sander, T.3
Steinlein, O.4
Hajnal, B.5
-
12
-
-
0017655817
-
Ectopic neurons in the hippocampus of the postnatal rat exposed to methylazoxymethanol during foetal development
-
Singh S. Ectopic neurons in the hippocampus of the postnatal rat exposed to methylazoxymethanol during foetal development. Acta Neuropathol (1977) 40:111-6. doi:10.1007/BF00688698
-
(1977)
Acta Neuropathol
, vol.40
, pp. 111-116
-
-
Singh, S.1
-
13
-
-
0035449480
-
Hippocampal heterotopia lack of functional Kv4.2 potassium channels in the methylazoxymethanol model of cortical malformation and epilepsy
-
Castro P, Cooper E, Lowenstein D, Baraban S. Hippocampal heterotopia lack of functional Kv4.2 potassium channels in the methylazoxymethanol model of cortical malformation and epilepsy. J Neurosci (2001) 21:6626-34
-
(2001)
J Neurosci
, vol.21
, pp. 6626-6634
-
-
Castro, P.1
Cooper, E.2
Lowenstein, D.3
Baraban, S.4
-
14
-
-
84856147573
-
KCNQ2 Encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy
-
Weckhuysen S, Mandelstam S, Suls A, Audenaert D, Deconinck T, Claes L, et al. KCNQ2 Encephalopathy: emerging phenotype of a neonatal epileptic encephalopathy. Ann Neurol (2012) 71:15-25. doi:10.1002/ana.22644
-
(2012)
Ann Neurol
, vol.71
, pp. 15-25
-
-
Weckhuysen, S.1
Mandelstam, S.2
Suls, A.3
Audenaert, D.4
Deconinck, T.5
Claes, L.6
-
15
-
-
84865611065
-
Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome
-
Saitsu H, Kato M, Koide A, Goto T, Fujita T, Nishiyama K, et al. Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome. Ann Neurol (2012) 72:298-300. doi:10.1002/ana.23620
-
(2012)
Ann Neurol
, vol.72
, pp. 298-300
-
-
Saitsu, H.1
Kato, M.2
Koide, A.3
Goto, T.4
Fujita, T.5
Nishiyama, K.6
-
16
-
-
84895767176
-
KCNQ2 encephalopathy; delineation of the electroclinical phenotype and treatment response
-
Numis A, Angriman M, Sullivan J, Lewis A, Striano P, Nabbout R, et al. KCNQ2 encephalopathy; delineation of the electroclinical phenotype and treatment response. Neurology (2014) 82:368-70. doi:10.1212/WNL.0000000000000060
-
(2014)
Neurology
, vol.82
, pp. 368-370
-
-
Numis, A.1
Angriman, M.2
Sullivan, J.3
Lewis, A.4
Striano, P.5
Nabbout, R.6
-
17
-
-
84880461745
-
Video/EEG findings in a KCNQ2 epileptic encephalopathy: a case report and revision of literature data
-
Serino D, Specchio N, Pontrelli G, Vigevano F, Fusco L. Video/EEG findings in a KCNQ2 epileptic encephalopathy: a case report and revision of literature data. Epileptic Disord (2013) 15:158-65. doi:10.1684/epd.2013.0578
-
(2013)
Epileptic Disord
, vol.15
, pp. 158-165
-
-
Serino, D.1
Specchio, N.2
Pontrelli, G.3
Vigevano, F.4
Fusco, L.5
-
18
-
-
84878005306
-
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2
-
Milh M, Boutry-Kryza N, Sutera-sardo J, Mognot C, Auvin S, Lacoste C, et al. Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2. Orphanet J Rare Dis (2013) 8:80. doi:10.1186/1750-1172-8-80
-
(2013)
Orphanet J Rare Dis
, vol.8
, pp. 80
-
-
Milh, M.1
Boutry-Kryza, N.2
Sutera-sardo, J.3
Mognot, C.4
Auvin, S.5
Lacoste, C.6
-
19
-
-
34548620484
-
Properties of persistent postnatal cortical subplate neurons
-
Torres-Reveron J, Friedlander MJ. Properties of persistent postnatal cortical subplate neurons. J Neurosci (2007) 27:9962-74. doi:10.1523/JNEUROSCI.1536-07.2007
-
(2007)
J Neurosci
, vol.27
, pp. 9962-9974
-
-
Torres-Reveron, J.1
Friedlander, M.J.2
-
20
-
-
70449675022
-
Malformations of cortical development and epilepsies: neuropathological findings with emphasis on focal cortical dysplasia
-
Blümcke I, Vinters HV, Armstrong D, Aronica E, Thom M, Spreaficio R. Malformations of cortical development and epilepsies: neuropathological findings with emphasis on focal cortical dysplasia. Epileptic Disord (2009) 11:181-93. doi:10.1684/epd.2009.0261
-
(2009)
Epileptic Disord
, vol.11
, pp. 181-193
-
-
Blümcke, I.1
Vinters, H.V.2
Armstrong, D.3
Aronica, E.4
Thom, M.5
Spreaficio, R.6
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