-
2
-
-
0028011992
-
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder
-
Scheffer IE, Bhatia KP, Lopes-Cendes I, et al. Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder. Lancet 1994; 343:515-7.
-
(1994)
Lancet
, vol.343
, pp. 515-517
-
-
Scheffer, I.E.1
Bhatia, K.P.2
Lopes-Cendes, I.3
-
3
-
-
0028900303
-
Autosomal dominant nocturnal frontal lobe epilepsy: A distinctive clinical disorder
-
Scheffer IE, Bhatia KP, Lopes-Cendes I, et al. Autosomal dominant nocturnal frontal lobe epilepsy: a distinctive clinical disorder. Brain 1995; 118:61-73.
-
(1995)
Brain
, vol.118
, pp. 61-73
-
-
Scheffer, I.E.1
Bhatia, K.P.2
Lopes-Cendes, I.3
-
4
-
-
0029045967
-
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2
-
Phillips HA, Scheffer IE, Bercovic SF, Hollway GE. Sutherland GR, Mulley JC. Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2. Nature Genet 1995;10:117-8.
-
(1995)
Nature Genet
, vol.10
, pp. 117-118
-
-
Phillips, H.A.1
Scheffer, I.E.2
Bercovic, S.F.3
Hollway, G.E.4
Sutherland, G.R.5
Mulley, J.C.6
-
5
-
-
0028980028
-
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
-
Steinlein OK, Mulley JC, Propping P, et al. A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy. Nature Genet 1995;11:201-3.
-
(1995)
Nature Genet
, vol.11
, pp. 201-203
-
-
Steinlein, O.K.1
Mulley, J.C.2
Propping, P.3
-
6
-
-
0029788681
-
Autosomal dominant nocturnal frontal lobe epilepsy: Electroclinical picture
-
Oldani A, Zucconi M, Ferini-Strambi L, Bizzozero D, Smirne S. Autosomal dominant nocturnal frontal lobe epilepsy: electroclinical picture. Epilepsia 1996;37:964-76.
-
(1996)
Epilepsia
, vol.37
, pp. 964-976
-
-
Oldani, A.1
Zucconi, M.2
Ferini-Strambi, L.3
Bizzozero, D.4
Smirne, S.5
-
7
-
-
0030916583
-
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
-
Steinlein OK, Magnusson A, Stoodt J, et al. An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy. Human Mol Genet 1997;6:943-7.
-
(1997)
Human Mol Genet
, vol.6
, pp. 943-947
-
-
Steinlein, O.K.1
Magnusson, A.2
Stoodt, J.3
-
8
-
-
0030602149
-
An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics
-
Weiland S, Witzemann V, Villarroel A, Propping P, Steinlein OK. An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics. FEBS Lett 1996;398:91-6.
-
(1996)
FEBS Lett
, vol.398
, pp. 91-96
-
-
Weiland, S.1
Witzemann, V.2
Villarroel, A.3
Propping, P.4
Steinlein, O.K.5
-
10
-
-
0029206702
-
Frontal lobe epilepsy: Some clinical characteristics
-
Jasper HH, Riggio S, Goldman-Rakic PS, eds. Adv Neurol; New York: Raven Press
-
Williamson PD. Frontal lobe epilepsy: some clinical characteristics. In: Jasper HH, Riggio S, Goldman-Rakic PS, eds. Epilepsy and the functional anatomy of the frontal lobe. (Adv Neurol; vol 66). New York: Raven Press, 1995:127-52.
-
(1995)
Epilepsy and the Functional Anatomy of the Frontal Lobe
, vol.66
, pp. 127-152
-
-
Williamson, P.D.1
-
11
-
-
0025613019
-
Mesial frontal lobe epilepsy: A clinical entity not sufficiently described
-
Fusco L, Iani C, Faedda MT, et al. Mesial frontal lobe epilepsy: a clinical entity not sufficiently described. J Epilepsy 1990;3:123-35.
-
(1990)
J Epilepsy
, vol.3
, pp. 123-135
-
-
Fusco, L.1
Iani, C.2
Faedda, M.T.3
-
12
-
-
0027406988
-
Hypnic tonic postural seizures in healthy children provide evidence for a partial epileptic syndrome of frontal lobe origin
-
Vigevano F, Fusco L. Hypnic tonic postural seizures in healthy children provide evidence for a partial epileptic syndrome of frontal lobe origin. Epilepsia 1993;39:110-9.
-
(1993)
Epilepsia
, vol.39
, pp. 110-119
-
-
Vigevano, F.1
Fusco, L.2
-
13
-
-
0026543705
-
Is nocturnal paroxysmal dystonia a form of frontal lobe epilepsy?
-
Meiercord H, Fish DR, Smith SJM, Scott CA, Shorvon SD, Marsden CD. Is nocturnal paroxysmal dystonia a form of frontal lobe epilepsy? Mov Disord 1992;7:38-42.
-
(1992)
Mov Disord
, vol.7
, pp. 38-42
-
-
Meiercord, H.1
Fish, D.R.2
Smith, S.J.M.3
Scott, C.A.4
Shorvon, S.D.5
Marsden, C.D.6
-
14
-
-
0028319184
-
Nocturnal paroxysmal dystonia: A clinical form of focal epilepsy
-
Hirsch E, Sellal F, Maton B, Rumbach L, Marescaux C. Nocturnal paroxysmal dystonia: a clinical form of focal epilepsy. Neurophysiol Clin 1994;24:207-17.
-
(1994)
Neurophysiol Clin
, vol.24
, pp. 207-217
-
-
Hirsch, E.1
Sellal, F.2
Maton, B.3
Rumbach, L.4
Marescaux, C.5
-
15
-
-
0026456748
-
Electroclinical symptomatology of partial seizures of orbital frontal origin
-
Chauvel P, Delgado-Escueta AV, Halgren E, Bancaud J, eds. Adv Neurol; New York: Raven Press
-
Munari C, Bancaud J. Electroclinical symptomatology of partial seizures of orbital frontal origin. In: Chauvel P, Delgado-Escueta AV, Halgren E, Bancaud J, eds. Frontal lobe seizures and epilepsies. (Adv Neurol; vol 57). New York: Raven Press, 1992:257-66.
-
(1992)
Frontal Lobe Seizures and Epilepsies
, vol.57
, pp. 257-266
-
-
Munari, C.1
Bancaud, J.2
-
16
-
-
0029083471
-
Frontal lobe epilepsy: Clinical syndromes and presurgical evaluation
-
Riggio S. Frontal lobe epilepsy: clinical syndromes and presurgical evaluation. J Epilepsy 1995;8:178-89.
-
(1995)
J Epilepsy
, vol.8
, pp. 178-189
-
-
Riggio, S.1
-
17
-
-
0027445242
-
Thalamocortical oscillations in the sleeping and aroused brain
-
Steriade M, McCormick DA, Sejnowski TJ. Thalamocortical oscillations in the sleeping and aroused brain. Science 1993;262:679-85.
-
(1993)
Science
, vol.262
, pp. 679-685
-
-
Steriade, M.1
McCormick, D.A.2
Sejnowski, T.J.3
-
18
-
-
8544254723
-
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
-
Elmslie FV, Rees M, Williamson MP, et al. Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. Hum Mol Genet 1997;6:1329-34.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1329-1334
-
-
Elmslie, F.V.1
Rees, M.2
Williamson, M.P.3
-
19
-
-
0030116489
-
The genetics of idiopathic generalized epilepsy: Implications for the understanding of its aetiology
-
Sander T. The genetics of idiopathic generalized epilepsy: implications for the understanding of its aetiology. Mol Med Today 1996;2:173-80.
-
(1996)
Mol Med Today
, vol.2
, pp. 173-180
-
-
Sander, T.1
-
20
-
-
0031594666
-
1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy
-
1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy. Epilepsy Res 1998;29:115-22.
-
(1998)
Epilepsy Res
, vol.29
, pp. 115-122
-
-
Sander, T.1
Peters, C.2
Janz, D.3
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