-
1
-
-
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;343:515-517
-
(1994)
Lancet
, vol.343
, pp. 515-517
-
-
Scheffer, I.E.1
Bhatia, K.P.2
Lopes-Cendes, I.3
-
2
-
-
0029059069
-
Localization of a gene for partial epilepsy to chromosome 10q
-
Ottman R, Risch N, Hauser WA, et al. Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet 1995;10: 56-60
-
(1995)
Nat Genet
, vol.10
, pp. 56-60
-
-
Ottman, R.1
Risch, N.2
Hauser, W.A.3
-
3
-
-
0029084895
-
Autosomal dominant Rolandic epilepsy and speech dyspraxia: A new syndrome with anticipation
-
Scheffer IE, Jones L, Pozzebon M, et al. Autosomal dominant Rolandic epilepsy and speech dyspraxia: a new syndrome with anticipation. Ann Neurol 1995;38:633-642
-
(1995)
Ann Neurol
, vol.38
, pp. 633-642
-
-
Scheffer, I.E.1
Jones, L.2
Pozzebon, M.3
-
4
-
-
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
-
6
-
-
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
-
7
-
-
0030697469
-
Autosomal dominant nocturnal frontal lobe epilepsy: Demonstration of focal frontal onset and intrafamilial variation
-
Hayman M, Scheffer IE, Chinvarun Y, et al. 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
-
8
-
-
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. 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
-
9
-
-
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. Hum Mol Genet 1997;6: 943-948
-
(1997)
Hum Mol Genet
, vol.6
, pp. 943-948
-
-
Steinlein, O.K.1
Magnusson, A.2
Stoodt, J.3
-
10
-
-
0000025825
-
Genetic heterogeneity in autosomal dominant nocturnal frontal lobe epilepsy
-
Abstract
-
Berkovic SF, Phillips HA, Scheffer IE, et al. Genetic heterogeneity in autosomal dominant nocturnal frontal lobe epilepsy. Epilepsia 1995;36:147 (Abstract)
-
(1995)
Epilepsia
, vol.36
, pp. 147
-
-
Berkovic, S.F.1
Phillips, H.A.2
Scheffer, I.E.3
-
12
-
-
0342435720
-
Autosomal dominant partial epilepsy with variable foci is not allelic with autosomal dominant nocturnal frontal lobe epilepsy
-
Abstract
-
Scheffer IE, Phillips H, Mulley J, et al. Autosomal dominant partial epilepsy with variable foci is not allelic with autosomal dominant nocturnal frontal lobe epilepsy. Epilepsia 1995;36: S28 (Abstract)
-
(1995)
Epilepsia
, vol.36
-
-
Scheffer, I.E.1
Phillips, H.2
Mulley, J.3
-
15
-
-
0025024657
-
Prediction of verbal, performance, and full scale IQs from seven subtests of the WAIS-R
-
Ward C. Prediction of verbal, performance, and full scale IQs from seven subtests of the WAIS-R. J Clin Psychol 1990;46: 436-440
-
(1990)
J Clin Psychol
, vol.46
, pp. 436-440
-
-
Ward, C.1
-
16
-
-
0030044668
-
Pedigree analysis in families with febrile seizures
-
Johnson WG, Kugler SL, Stenroos ES, et al. Pedigree analysis in families with febrile seizures. Am J Med Genet 1996;61: 345-352
-
(1996)
Am J Med Genet
, vol.61
, pp. 345-352
-
-
Johnson, W.G.1
Kugler, S.L.2
Stenroos, E.S.3
-
17
-
-
0000801438
-
SLINK: A general simulation program for linkage analysis
-
Abstract
-
Weeks DE, Ott J, Lathrop GM. SLINK: a general simulation program for linkage analysis. Am J Hum Genet 1990;47:A204 (Abstract)
-
(1990)
Am J Hum Genet
, vol.47
-
-
Weeks, D.E.1
Ott, J.2
Lathrop, G.M.3
-
18
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996;380:152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
-
19
-
-
0029045967
-
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2
-
Phillips HA, Scheffer IE, Berkovic SF, et al. Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2. Nat Genet 1995;10:117-118
-
(1995)
Nat Genet
, vol.10
, pp. 117-118
-
-
Phillips, H.A.1
Scheffer, I.E.2
Berkovic, S.F.3
-
20
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop GM, Lalouel JM. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 1984;36: 460-465
-
(1984)
Am J Hum Genet
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
21
-
-
0027432652
-
Incorrect specification of marker allele frequencies: Effects on linkage analysis
-
Freimer NB, Sandkuijl LA, Blower SM. Incorrect specification of marker allele frequencies: Effects on linkage analysis. Am J Hum Genet 1993;52:1102-1110
-
(1993)
Am J Hum Genet
, vol.52
, pp. 1102-1110
-
-
Freimer, N.B.1
Sandkuijl, L.A.2
Blower, S.M.3
-
22
-
-
0023205323
-
Exclusion mapping
-
Edwards JH. Exclusion mapping. J Med Genet 1987;24:539-543
-
(1987)
J Med Genet
, vol.24
, pp. 539-543
-
-
Edwards, J.H.1
-
23
-
-
0031050270
-
Epilepsies with single gene inheritance
-
Berkovic SF, Scheffer IE. Epilepsies with single gene inheritance. Brain Dev 1997;19:13-18
-
(1997)
Brain Dev
, vol.19
, pp. 13-18
-
-
Berkovic, S.F.1
Scheffer, I.E.2
-
25
-
-
0008302433
-
Verbal memory in temporal lobe epilepsy: Cognitive influences and task-specific effects
-
Saling MM, O'Shea MF, Berkovic SF. Verbal memory in temporal lobe epilepsy: cognitive influences and task-specific effects. Epilepsia 1995;36:93-94
-
(1995)
Epilepsia
, vol.36
, pp. 93-94
-
-
Saling, M.M.1
O'Shea, M.F.2
Berkovic, S.F.3
-
26
-
-
0016808239
-
Benign epilepsy of childhood with centrotemporal EEG foci: A genetic study
-
Heijbel J, Blom S, Rasmuson M. Benign epilepsy of childhood with centrotemporal EEG foci: a genetic study. Epilepsia 1975; 16:285-293
-
(1975)
Epilepsia
, vol.16
, pp. 285-293
-
-
Heijbel, J.1
Blom, S.2
Rasmuson, M.3
-
28
-
-
85038547283
-
Characterization of a new ion channel gene candidate for benign familial neonatal convulsions
-
Abstract
-
Charlier C, Singh N, Stauffer D, et al. Characterization of a new ion channel gene candidate for benign familial neonatal convulsions. Am J Hum Genet 1997;61:A271 (Abstract)
-
(1997)
Am J Hum Genet
, vol.61
-
-
Charlier, C.1
Singh, N.2
Stauffer, D.3
-
29
-
-
0032536030
-
A potassium channel mutation in neonatal human epilepsy
-
Biervert C, Schroeder BC, Kubisch C, et al. A potassium channel mutation in neonatal human epilepsy. Science 1998;279: 403-406
-
(1998)
Science
, vol.279
, pp. 403-406
-
-
Biervert, C.1
Schroeder, B.C.2
Kubisch, C.3
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