-
1
-
-
13044266230
-
Classification of the epilepsies
-
Edited by Wyllie E. Baltimore: Williams & Wilkins;
-
Wyllie E, Lüders H: Classification of the epilepsies. In The Treatment of Epilepsy: Principles and Practice. Edited by Wyllie E. Baltimore: Williams & Wilkins; 1997:364-366.
-
(1997)
The Treatment of Epilepsy: Principles and Practice
, pp. 364-366
-
-
Wyllie, E.1
Lüders, H.2
-
2
-
-
0001980025
-
Infantile spasms and West syndrome
-
Edited by Engel JJ, Pedley TA. Philadelphia: Lippincott-Raven
-
Dulac O: Infantile spasms and West syndrome. In Epilepsy: A Comprehensive Textbook. Edited by Engel JJ, Pedley TA. Philadelphia: Lippincott-Raven, 1989:2277-2283.
-
(1989)
Epilepsy: A Comprehensive Textbook
, pp. 2277-2283
-
-
Dulac, O.1
-
3
-
-
0031938905
-
West syndrome: Etiological and prognostic aspects
-
Watanabe K: West syndrome: etiological and prognostic aspects. Brain Devel 1998, 20:1-8. An excellent and comprehensive review on the pathogenesis of one of the serious catastrophic epilepsies of early infancy.
-
(1998)
Brain Devel
, vol.20
, pp. 1-8
-
-
Watanabe, K.1
-
4
-
-
0000832868
-
Lennox-Gastaut syndrome and other childhood epileptic encephalopathies
-
Edited by Engel JJ, Pedley TA. Philadelphia: Lippincott-Raven
-
Genton P, Dravet C: Lennox-Gastaut syndrome and other childhood epileptic encephalopathies. In Epilepsy: A Comprehensive Textbook. Edited by Engel JJ, Pedley TA. Philadelphia: Lippincott-Raven, 1998: 2355-2366.
-
(1998)
Epilepsy: A Comprehensive Textbook
, pp. 2355-2366
-
-
Genton, P.1
Dravet, C.2
-
6
-
-
0031066631
-
Local-clonal expansion of infiltrating T lymphocytes in chronic encephalitis of Rasmussen
-
Li Y, Uccelli A, Laxer KD, Jeong MC, Vinters HV, Tourtellotte WW, et al.: Local-clonal expansion of infiltrating T lymphocytes in chronic encephalitis of Rasmussen. J Immunol 1997, 158:1428-1437.
-
(1997)
J Immunol
, vol.158
, pp. 1428-1437
-
-
Li, Y.1
Uccelli, A.2
Laxer, K.D.3
Jeong, M.C.4
Vinters, H.V.5
Tourtellotte, W.W.6
-
7
-
-
0031897349
-
Double pathology in Rasmussen's syndrome: A window on the etiology?
-
Hart YM, Andermann F, Robitaille Y, Laxer KD, Rasmussen T, Davis R: Double pathology in Rasmussen's syndrome: a window on the etiology? Neurology 1998, 50:731-735.
-
(1998)
Neurology
, vol.50
, pp. 731-735
-
-
Hart, Y.M.1
Andermann, F.2
Robitaille, Y.3
Laxer, K.D.4
Rasmussen, T.5
Davis, R.6
-
8
-
-
0030721561
-
Temporal lobe epilepsy in childhood: Clinical, EEG, and neuroimaging findings and syndrome classification in a cohort with new-onset seizures
-
Harvey AS, Berkovic SF, Wrennall JA, Hopkins U: Temporal lobe epilepsy in childhood: clinical, EEG, and neuroimaging findings and syndrome classification in a cohort with new-onset seizures. Neurology 1997, 49:960-968. A good correlative paper that is helpful to the clinician in approaching TLE in childhood.
-
(1997)
Neurology
, vol.49
, pp. 960-968
-
-
Harvey, A.S.1
Berkovic, S.F.2
Wrennall, J.A.3
Hopkins, U.4
-
9
-
-
0031942864
-
Temporal lobe developmental malformations and epilepsy: Dual pathology and bilateral hippocampal abnormalities
-
Ho SS, Kuzniecky RI, Gilliam F, Faught E, Morawetz R: Temporal lobe developmental malformations and epilepsy: dual pathology and bilateral hippocampal abnormalities. Neurology 1998, 50:748-754.
-
(1998)
Neurology
, vol.50
, pp. 748-754
-
-
Ho, S.S.1
Kuzniecky, R.I.2
Gilliam, F.3
Faught, E.4
Morawetz, R.5
-
10
-
-
0030907041
-
Dentate granule cell neurogenesis is increased by seizures and contributes to aberrant network reorganization in the adult rat hippocampus
-
Parent JM, Yu TW, Leibowitz RT, Geschwind DH, Slovrter RS, Lowenstein DH: Dentate granule cell neurogenesis is increased by seizures and contributes to aberrant network reorganization in the adult rat hippocampus. J Neurosci 1997, 17:3727-3738. This paper describes granule cell neurogenesis and migration in the mature rat hippocampus as a consequence of seizures thus stimulating radically new ways of thinking about mechanisms of epileptogenesis.
-
(1997)
J Neurosci
, vol.17
, pp. 3727-3738
-
-
Parent, J.M.1
Yu, T.W.2
Leibowitz, R.T.3
Geschwind, D.H.4
Slovrter, R.S.5
Lowenstein, D.H.6
-
11
-
-
0030835301
-
The clinical syndrome of early-life bilateral hippocampal sclerosis
-
DeLong GR, Heinz ER: The clinical syndrome of early-life bilateral hippocampal sclerosis. Ann Neurol 1997, 42:11-17.
-
(1997)
Ann Neurol
, vol.42
, pp. 11-17
-
-
DeLong, G.R.1
Heinz, E.R.2
-
12
-
-
0030822047
-
Pediatric congenital bilateral perisylvian syndrome: Clinical and MRI features in 12 patients
-
Gropman AL, Barkovich AJ, Vezina LG, Conry JA, Dubovsky EC, Packer RJ: Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients. Neuropediatrics 1997, 28:198-203.
-
(1997)
Neuropediatrics
, vol.28
, pp. 198-203
-
-
Gropman, A.L.1
Barkovich, A.J.2
Vezina, L.G.3
Conry, J.A.4
Dubovsky, E.C.5
Packer, R.J.6
-
13
-
-
18244413664
-
Bilateral parasagittal parietooccipital polymicrogyria and epilepsy
-
Guerrini R, Dubeau F, Dulac O, Barkovich AJ, Kuzniecky R, Fett C, et al.: Bilateral parasagittal parietooccipital polymicrogyria and epilepsy [see comments]. Ann Neurol 1997, 41:65-73.
-
(1997)
Ann Neurol
, vol.41
, pp. 65-73
-
-
Guerrini, R.1
Dubeau, F.2
Dulac, O.3
Barkovich, A.J.4
Kuzniecky, R.5
Fett, C.6
-
14
-
-
0032536030
-
A potassium channel mutation in neonatal human epilepsy
-
Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, et al.: A potassium channel mutation in neonatal human epilepsy. Science 1998, 279:403-406. The authors have isolated the first gene specifically identifiable with human IGE and demonstrate with an in vitro expression system that the gene product may impair cellular repolarization leading to neuronal hyperexcitability (see also Singh et al., Not Genet 1998, 18:25-29).
-
(1998)
Science
, vol.279
, pp. 403-406
-
-
Biervert, C.1
Schroeder, B.C.2
Kubisch, C.3
Berkovic, S.F.4
Propping, P.5
Jentsch, T.J.6
-
15
-
-
17344372328
-
-
Biervert C, Schroeder BC, Kubisch C, Berkovic SF, Propping P, Jentsch TJ, et al.: A potassium channel mutation in neonatal human epilepsy. Science 1998, 279:403-406. The authors have isolated the first gene specifically identifiable with human IGE and demonstrate with an in vitro expression system that the gene product may impair cellular repolarization leading to neuronal hyperexcitability (see also Singh et al., Not Genet 1998, 18:25-29).
-
(1998)
Not Genet
, vol.18
, pp. 25-29
-
-
Singh1
-
16
-
-
17344372328
-
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
-
Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, et al.: A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns [see comments]. Nat Genet 1998, 18:25-29. Concurrent (See also Biervert et al., Science 1998, 279:403-406) description of the first gene specifically identifiable with an idiopathic generalized human epilepsy, and identification of various individual mutations of this gene in affected persons.
-
(1998)
Nat Genet
, vol.18
, pp. 25-29
-
-
Singh, N.A.1
Charlier, C.2
Stauffer, D.3
DuPont, B.R.4
Leach, R.J.5
Melis, R.6
-
17
-
-
0032536030
-
-
Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, et al.: A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns [see comments]. Nat Genet 1998, 18:25-29. Concurrent (See also Biervert et al., Science 1998, 279:403-406) description of the first gene specifically identifiable with an idiopathic generalized human epilepsy, and identification of various individual mutations of this gene in affected persons.
-
(1998)
Science
, vol.279
, pp. 403-406
-
-
Biervert1
-
18
-
-
0031974209
-
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
-
Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, et al.: A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family [see comments]. Nat Genet 1998, 18:53-55.
-
(1998)
Nat Genet
, vol.18
, pp. 53-55
-
-
Charlier, C.1
Singh, N.A.2
Ryan, S.G.3
Lewis, T.B.4
Reus, B.E.5
Leach, R.J.6
-
19
-
-
0031974740
-
Epilepsy genes: Excitement traced to potassium channels
-
Stoffel M, Jan LY: Epilepsy genes: excitement traced to potassium channels [news; comment]. Nat Genet 1998, 18:6-8.
-
(1998)
Nat Genet
, vol.18
, pp. 6-8
-
-
Stoffel, M.1
Jan, L.Y.2
-
20
-
-
0031016163
-
Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2
-
Signorini S, Liao YJ, Duncan SA, Jan LY, Stoffel M: Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2. Proc Nat Acad Sci U S A 1997, 94:923-927.
-
(1997)
Proc Nat Acad Sci U S A
, vol.94
, pp. 923-927
-
-
Signorini, S.1
Liao, Y.J.2
Duncan, S.A.3
Jan, L.Y.4
Stoffel, M.5
-
21
-
-
0030614535
-
Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (Ih) mouse
-
Burgess DL, Jones JM, Meisler MH, Noebels JL: Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (Ih) mouse. Cell 1997, 88:385-392.
-
(1997)
Cell
, vol.88
, pp. 385-392
-
-
Burgess, D.L.1
Jones, J.M.2
Meisler, M.H.3
Noebels, J.L.4
-
22
-
-
0030584085
-
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
-
Fletcher CF, Lutz CM, O'Sullivan TN, Shaughnessy JD Jr, Hawkes R, Frankel WW, et al.: Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell 1996, 87:607-617.
-
(1996)
Cell
, vol.87
, pp. 607-617
-
-
Fletcher, C.F.1
Lutz, C.M.2
O'Sullivan, T.N.3
Shaughnessy Jr., J.D.4
Hawkes, R.5
Frankel, W.W.6
-
23
-
-
12644290240
-
Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior
-
Homanics GE, DeLorey TM, Firestone LL, Quinlan JJ, Handforth A, Harrison NL, et al.: Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior. Proc Nat Acad Sci U S A 1997, 94:4143-4148.
-
(1997)
Proc Nat Acad Sci U S A
, vol.94
, pp. 4143-4148
-
-
Homanics, G.E.1
DeLorey, T.M.2
Firestone, L.L.3
Quinlan, J.J.4
Handforth, A.5
Harrison, N.L.6
-
24
-
-
0031594666
-
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy
-
Sander T, Peters C, Janz D, Bianchi A, Bauer G, Wienker TF, et al.: The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy. Epilepsy Res 1998, 29:115-122.
-
(1998)
Epilepsy Res
, vol.29
, pp. 115-122
-
-
Sander, T.1
Peters, C.2
Janz, D.3
Bianchi, A.4
Bauer, G.5
Wienker, T.F.6
-
25
-
-
0030670298
-
Epilepsy genes and the genetics of epilepsy syndromes: The promise of new therapies based on genetic knowledge
-
Berkovic SF: Epilepsy genes and the genetics of epilepsy syndromes: the promise of new therapies based on genetic knowledge. Epilepsia 1997, 38(suppl 9):S32-S36.
-
(1997)
Epilepsia
, vol.38
, Issue.9 SUPPL.
-
-
Berkovic, S.F.1
-
26
-
-
8544269355
-
Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alphas, beta3 and gamma3 subunit gene cluster on chromosome 15
-
Sander T, Kretz R, Williamson MP, Elmslie FV, Rees M, Hildmann T, et al.: Linkage analysis between idiopathic generalized epilepsies and the GABA(A) receptor alphas, beta3 and gamma3 subunit gene cluster on chromosome 15. Acta Neurol Scand 1997, 96:1-7.
-
(1997)
Acta Neurol Scand
, vol.96
, pp. 1-7
-
-
Sander, T.1
Kretz, R.2
Williamson, M.P.3
Elmslie, F.V.4
Rees, M.5
Hildmann, T.6
-
27
-
-
0030749655
-
Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies
-
Steinlein O, Sander T, Stoodt J, Kretz R, Janz D, Propping P: Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies. Am J Med Genet 1997, 74:445-449.
-
(1997)
Am J Med Genet
, vol.74
, pp. 445-449
-
-
Steinlein, O.1
Sander, T.2
Stoodt, J.3
Kretz, R.4
Janz, D.5
Propping, P.6
-
28
-
-
0031978045
-
Segregation analysis in typical absence epilepsy
-
Buoni S, Grosso S, Di Cosmo G, Di Bartolo RM, Di Marco V, Fois A: Segregation analysis in typical absence epilepsy. J Child Neurol 1998, 13:89-93.
-
(1998)
J Child Neurol
, vol.13
, pp. 89-93
-
-
Buoni, S.1
Grosso, S.2
Di Cosmo, G.3
Di Bartolo, R.M.4
Di Marco, V.5
Fois, A.6
-
29
-
-
0030757806
-
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism
-
Sander T, Hildmann T, Kretz R, Fürst R, Sailer U, Bauer G, et al.: Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism. Am J Med Genet 1997, 74:416-421.
-
(1997)
Am J Med Genet
, vol.74
, pp. 416-421
-
-
Sander, T.1
Hildmann, T.2
Kretz, R.3
Fürst, R.4
Sailer, U.5
Bauer, G.6
-
30
-
-
8544254723
-
Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q
-
Elmslie FV, Rees M, Williamson MP, Kerr M, Kjeldsen MJ, Pang KA, et al.: Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. Hum Mol Genet 1997, 6:1329-1334.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1329-1334
-
-
Elmslie, F.V.1
Rees, M.2
Williamson, M.P.3
Kerr, M.4
Kjeldsen, M.J.5
Pang, K.A.6
-
31
-
-
8044248429
-
Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q
-
Guipponi M, Rivier F, Vigevano F, Beck C, Crespel A, Echenne B, et al.: Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q. Hum Mol Genet 1997, 6:473-477.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 473-477
-
-
Guipponi, M.1
Rivier, F.2
Vigevano, F.3
Beck, C.4
Crespel, A.5
Echenne, B.6
-
32
-
-
0028980028
-
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
-
Steinlein OK, Mulley JC, Propping P, Wallace RH, Phillips HA, Sutherland GR, et al.: A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy. Nat Genet 1995, 11:201-203.
-
(1995)
Nat Genet
, vol.11
, pp. 201-203
-
-
Steinlein, O.K.1
Mulley, J.C.2
Propping, P.3
Wallace, R.H.4
Phillips, H.A.5
Sutherland, G.R.6
-
33
-
-
0030916583
-
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
-
Steinlein OK, Magnusson A, Stoodt J, Bertrand S, Weiland S, Berkovic SF, et al.: An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy. Hum Mol Genet 1997, 6:943-947.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 943-947
-
-
Steinlein, O.K.1
Magnusson, A.2
Stoodt, J.3
Bertrand, S.4
Weiland, S.5
Berkovic, S.F.6
-
34
-
-
0031931373
-
Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome
-
Oldani A, Zucconi M, Asselta R, Modugno M, Bonati MT, Dalprà L, et al.: Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome. Brain 1998, 121:205-223.
-
(1998)
Brain
, vol.121
, pp. 205-223
-
-
Oldani, A.1
Zucconi, M.2
Asselta, R.3
Modugno, M.4
Bonati, M.T.5
Dalprà, L.6
-
35
-
-
0030697469
-
Autosomal dominant nocturnal frontal lobe epilepsy: Demonstration of focal frontal onset and intrafamilial variation
-
Hayman M, Scheffer IE, Chinvarun Y, Berlangieri SU, Berkovic SF: Autosomal dominant nocturnal frontal lobe epilepsy: demonstration of focal frontal onset and intrafamilial variation. Neurology 1997, 49:969-975.
-
(1997)
Neurology
, vol.49
, pp. 969-975
-
-
Hayman, M.1
Scheffer, I.E.2
Chinvarun, Y.3
Berlangieri, S.U.4
Berkovic, S.F.5
-
36
-
-
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. Describes clinical heterogeneity in the familial form of an important epilepsy syndrome.
-
(1998)
Neurology
, vol.50
, pp. 554-557
-
-
Cendes, F.1
Lopes-Cendes, I.2
Andermann, E.3
Andermann, F.4
-
37
-
-
0344765463
-
Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis
-
Fernández G, Effenberger O, Vinz B, Steinlein O, Elger CE, Döhring W, et al.: Hippocampal malformation as a cause of familial febrile convulsions and subsequent hippocampal sclerosis [see comments]. Neurology 1998, 50:909-917. Using magnetic resonance imaging data, this paper addresses a long-standing controversy in epileptogenesis pertaining to the relationship between genetics, febrile seizures and hippocampal sclerosis.
-
(1998)
Neurology
, vol.50
, pp. 909-917
-
-
Fernández, G.1
Effenberger, O.2
Vinz, B.3
Steinlein, O.4
Elger, C.E.5
Döhring, W.6
-
38
-
-
0030854063
-
Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions
-
Neubauer BA, Moises HW, Lässker U, Waltz S, Diebold U, Stephani U: Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions. Epilepsia 1997, 38:782-787.
-
(1997)
Epilepsia
, vol.38
, pp. 782-787
-
-
Neubauer, B.A.1
Moises, H.W.2
Lässker, U.3
Waltz, S.4
Diebold, U.5
Stephani, U.6
-
39
-
-
0030894065
-
Benign rolandic epilepsy and chromosome 7q deletion
-
Burke MS, Carroll JE, Burket RC: Benign rolandic epilepsy and chromosome 7q deletion. J Child Neurol 1997, 12:148-149.
-
(1997)
J Child Neurol
, vol.12
, pp. 148-149
-
-
Burke, M.S.1
Carroll, J.E.2
Burket, R.C.3
-
40
-
-
0031945667
-
Febrile seizures: Genetics and relationship to other epilepsy syndromes
-
Berkovic SF, Scheffer IE: Febrile seizures: genetics and relationship to other epilepsy syndromes. Curr Opin Neurol 1998, 11:129-134. This paper provides a concise overview of the genetics of febrile seizures and their relationship to other epileptic syndromes that develop later in life, including TLE. The authors argue the possibility that febrile seizures may not simply be a nonspecific marker of a lowered seizure threshold and that specific types of epilepsy may follow febrile seizures.
-
(1998)
Curr Opin Neurol
, vol.11
, pp. 129-134
-
-
Berkovic, S.F.1
Scheffer, I.E.2
-
41
-
-
0029881889
-
Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21
-
Wallace RH, Berkovic SF, Howell RA, Sutherland GR, Mulley JC: Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21. J Med Genet 1996, 33:308-312.
-
(1996)
J Med Genet
, vol.33
, pp. 308-312
-
-
Wallace, R.H.1
Berkovic, S.F.2
Howell, R.A.3
Sutherland, G.R.4
Mulley, J.C.5
-
42
-
-
6844240853
-
Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest
-
Johnson EW, Dubovsky J, Rich SS, O'Donovan CA, Orr HT, Anderson VE, et al.: Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest. Hum Mol Genet 1998, 7:63-67.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 63-67
-
-
Johnson, E.W.1
Dubovsky, J.2
Rich, S.S.3
O'Donovan, C.A.4
Orr, H.T.5
Anderson, V.E.6
-
43
-
-
0030943313
-
Generalized epilepsy with febrile seizures plus: A genetic disorder with heterogeneous clinical phenotypes
-
Scheffer IE, Berkovic SF: Generalized epilepsy with febrile seizures plus: a genetic disorder with heterogeneous clinical phenotypes. Brain 1997, 120:479-490.
-
(1997)
Brain
, vol.120
, pp. 479-490
-
-
Scheffer, I.E.1
Berkovic, S.F.2
-
44
-
-
17444444915
-
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
-
des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakolf A, Carrié A, et al.: A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 1998, 92:51-61.
-
(1998)
Cell
, vol.92
, pp. 51-61
-
-
Des Portes, V.1
Pinard, J.M.2
Billuart, P.3
Vinet, M.C.4
Koulakolf, A.5
Carrié, A.6
-
45
-
-
0032498306
-
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
-
Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Schelfer I, et al.: Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 1998, 92:63-72.
-
(1998)
Cell
, vol.92
, pp. 63-72
-
-
Gleeson, J.G.1
Allen, K.M.2
Fox, J.W.3
Lamperti, E.D.4
Berkovic, S.5
Schelfer, I.6
-
46
-
-
8244247118
-
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): A gene causing neuronal migration defects in human brain
-
Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, et al.: Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain. Hum Mol Genet 1997, 6:555-562.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 555-562
-
-
Ross, M.E.1
Allen, K.M.2
Srivastava, A.K.3
Featherstone, T.4
Gleeson, J.G.5
Hirsch, B.6
-
47
-
-
0030826427
-
Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia
-
Fink JM, Dobyns WB, Guerrini R, Hirsch BA: Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia. Am J Hum Genet 1997, 61:379-387.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 379-387
-
-
Fink, J.M.1
Dobyns, W.B.2
Guerrini, R.3
Hirsch, B.A.4
-
48
-
-
0031722380
-
Mechanisms of cerebral dysgenesis
-
Gressens P: Mechanisms of cerebral dysgenesis. Curr Opin Pediatr 1998, 10:556-560.
-
(1998)
Curr Opin Pediatr
, vol.10
, pp. 556-560
-
-
Gressens, P.1
-
49
-
-
0030879277
-
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34
-
van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, et al.: Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34. Science 1997, 277:805-808.
-
(1997)
Science
, vol.277
, pp. 805-808
-
-
Van Slegtenhorst, M.1
De Hoogt, R.2
Hermans, C.3
Nellist, M.4
Janssen, B.5
Verhoef, S.6
-
50
-
-
0030663735
-
Role of the tuberous sclerosis gene-2 product in cell cycle control: Loss of the tuberous sclerosis gene-2 induces quiescent cells to enter S phase
-
Soucek T, Pusch O, Wienecke R, DeClue JE, Hengstschläger M: Role of the tuberous sclerosis gene-2 product in cell cycle control: loss of the tuberous sclerosis gene-2 induces quiescent cells to enter S phase. J Biol Chem 1997, 272:29301-29308.
-
(1997)
J Biol Chem
, vol.272
, pp. 29301-29308
-
-
Soucek, T.1
Pusch, O.2
Wienecke, R.3
DeClue, J.E.4
Hengstschläger, M.5
|