-
1
-
-
0023117724
-
Factors prognostic of unprovoked seizures after febrile convulsions
-
Annegers, J.F., Hauser, W.A., Shirts, S.B., and Kurland, L.T. (1987). Factors prognostic of unprovoked seizures after febrile convulsions. N. Engl. J. Med. 316, 493-498. (Pubitemid 17035550)
-
(1987)
New England Journal of Medicine
, vol.316
, Issue.9
, pp. 493-498
-
-
Annegers, J.F.1
Hauser, W.A.2
Shirts, S.B.3
Kurland, L.T.4
-
2
-
-
0025234572
-
Recurrence of febrile convulsions in a population-based cohort
-
DOI 10.1016/0920-1211(90)90040-3
-
Annegers, J.F., Blakley, S.A., Allen Hauser, W., and Kurland, L.T. (1990). Recurrence of febrile convulsions in a population-based cohort. Epilepsy Res. 5, 209-216. (Pubitemid 20125550)
-
(1990)
Epilepsy Research
, vol.5
, Issue.3
, pp. 209-216
-
-
Annegers, J.F.1
Blakley, S.A.2
Hauser, W.A.3
Kurland, L.T.4
-
3
-
-
33747707462
-
A novel GABRG2 mutation associated with febrile seizures
-
DOI 10.1212/01.wnl.0000230145.73496.a2, PII 0000611420060822000033
-
Audenaert, D., Schwartz, E., Claeys, K.G., Claes, L., Deprez, L., Suls, A., Van Dyck, T., Lagae, L., Van Broeckhoven, C., Macdonald, R.L., et al. (2006). A novel GABRG2 mutation associated with febrile seizures. Neurology 67, 687-690. (Pubitemid 44273621)
-
(2006)
Neurology
, vol.67
, Issue.4
, pp. 687-690
-
-
Audenaert, D.1
Schwartz, E.2
Claeys, K.G.3
Claes, L.4
Deprez, L.5
Suls, A.6
Van Dyck, T.7
Lagae, L.8
Van Broeckhoven, C.9
Macdonald, R.L.10
De Jonghe, P.11
-
4
-
-
84866165696
-
Failure to find association between febrile seizures and SCN1A rs3812718 polymorphism in south Indian patients with mesial temporal lobe epilepsy and hippocampal sclerosis
-
Balan, S., Vellichirammal, N.N., Banerjee, M., and Radhakrishnan, K. (2012). Failure to find association between febrile seizures and SCN1A rs3812718 polymorphism in south Indian patients with mesial temporal lobe epilepsy and hippocampal sclerosis. Epilepsy Res. 101, 288-292.
-
(2012)
Epilepsy Res.
, vol.101
, pp. 288-292
-
-
Balan, S.1
Vellichirammal, N.N.2
Banerjee, M.3
Radhakrishnan, K.4
-
5
-
-
0033364824
-
A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33
-
DOI 10.1086/302593
-
Baulac, S., Gourfinkel-An, I., Picard, F., Rosenberg-Bourgin, M., Prud'homme, J.-F., Baulac, M., Brice, A., and LeGuern, E. (1999). A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33. Am. J. Hum. Genet. 65, 1078-1085. (Pubitemid 30462965)
-
(1999)
American Journal of Human Genetics
, vol.65
, Issue.4
, pp. 1078-1085
-
-
Baulac, S.1
Gourfinkel-An, I.2
Picard, F.3
Rosenberg-Bourgin, M.4
Prud'homme, J.-F.5
Baulac, M.6
Brice, A.7
LeGuern, E.8
-
6
-
-
0035030766
-
A receptor dysfunction in epilepsy: A mutation in the γ2-subunit gene
-
DOI 10.1038/88254
-
Baulac, S., Huberfeld, G., Gourfinkel-An, I., Mitropoulou, G., Beranger, A., Prud'homme, J.-F., Baulac, M., Brice, A., Bruzzone, R., and Leguern, E. (2001). First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the 2-subunit gene. Nature Genet. 28, 46-48. (Pubitemid 32405815)
-
(2001)
Nature Genetics
, vol.28
, Issue.1
, pp. 46-48
-
-
Baulac, S.1
Huberfeld, G.2
Gourfinkel-An, I.3
Mitropoulou, G.4
Beranger, A.5
Prud'homme, J.-F.6
Baulac, M.7
Brice, A.8
Bruzzone, R.9
LeGuern, E.10
-
7
-
-
0033544408
-
Childhood-onset epilepsy with and without preceding febrile seizures
-
Berg, A.T., Shinnar, S., Levy, S.R., and Testa, F.M. (1999). Childhood-onset epilepsy with and without preceding febrile seizures. Neurology 53, 1742.
-
(1999)
Neurology
, vol.53
, pp. 1742
-
-
Berg, A.T.1
Shinnar, S.2
Levy, S.R.3
Testa, F.M.4
-
8
-
-
0031748082
-
Epilepsies in twins: Genetics of the major epilepsy syndromes
-
DOI 10.1002/ana.410430405
-
Berkovic, S.F., Howell, R.A., Hay, D.A., and Hopper, J.L. (1998). Epilepsies in twins: genetics of the major epilepsy syndromes. Ann. Neurol. 43, 435-445. (Pubitemid 28231717)
-
(1998)
Annals of Neurology
, vol.43
, Issue.4
, pp. 435-445
-
-
Berkovic, S.F.1
Howell, R.A.2
Hay, D.A.3
Hopper, J.L.4
-
9
-
-
0029846598
-
A study of childhood febrile convulsions with particular reference to HHV-6 infection: Pathogenic considerations
-
Bertolani, M., Portolani, M., Marotti, F., Sabbattini, A., Chiossi, C., Bandieri, M., and Cavazzuti, G.B. (1996). A study of childhood febrile convulsions with particular reference to HHV-6 infection: pathogenic considerations. Childs Nerv. Syst. 12, 534-539. (Pubitemid 26341381)
-
(1996)
Child's Nervous System
, vol.12
, Issue.9
, pp. 534-539
-
-
Bertolani, M.F.1
Portolani, M.2
Marotti, F.3
Sabbattini, A.M.4
Chiossi, C.5
Bandieri, M.R.6
Cavazzuti, G.B.7
-
10
-
-
33947576551
-
Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients
-
DOI 10.1111/j.1468-1331.2007.01702.x
-
Blair, M.A., Ma, S., Abou-Khalil, B., and Hedera, P. (2007). Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients. Eur. J. Neurol. 14, 424-427. (Pubitemid 46481173)
-
(2007)
European Journal of Neurology
, vol.14
, Issue.4
, pp. 424-427
-
-
Blair, M.A.1
Ma, S.2
Abou-Khalil, B.3
Hedera, P.4
-
11
-
-
41749097834
-
Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy
-
Bovo, G., Diani, E., Bisulli, F., Di Bonaventura, C., Striano, P., Gambardella, A., Ferlazzo, E., Egeo, G., Mecarelli, O., Elia, M., et al. (2008). Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. Neurosci. Lett. 436, 23-26.
-
(2008)
Neurosci. Lett.
, vol.436
, pp. 23-26
-
-
Bovo, G.1
Diani, E.2
Bisulli, F.3
Di Bonaventura, C.4
Striano, P.5
Gambardella, A.6
Ferlazzo, E.7
Egeo, G.8
Mecarelli, O.9
Elia, M.10
-
12
-
-
75949105642
-
No major clinical impact of Val66Met BDNF gene polymorphism on temporal lobe epilepsy
-
Bragatti, J.A., Schenkel, L.C., Torres, C.M., Manfro, G.G., Blaya, C., Souza, A.C.d., Souza, D.O., Saraiva-Pereira, M.L., Jardim, L.B., Leistner-Segal, S., et al. (2010). No major clinical impact of Val66Met BDNF gene polymorphism on temporal lobe epilepsy. Epilepsy Res. 88, 108-111.
-
(2010)
Epilepsy Res.
, vol.88
, pp. 108-111
-
-
Bragatti, J.A.1
Schenkel, L.C.2
Torres, C.M.3
Manfro, G.G.4
Blaya, C.5
Souza, A.C.D.6
Souza, D.O.7
Saraiva-Pereira, M.L.8
Jardim, L.B.9
Leistner-Segal, S.10
-
13
-
-
0034949135
-
Lack of association between an interleukin 1 beta (IL-1β gene variation and refractory temporal lobe epilepsy
-
DOI 10.1046/j.1528-1157.2001.42900.x
-
Buono, R.J., Ferraro, T.N., O'Connor, M.J., Sperling, M.R., Ryan, S.G., Scattergood, T., Mulholland, N., Gilmore, J., Lohoff, F.W., and Berrettini, W.H. (2001). Lack of association between an interleukin 1 beta (IL-1) gene variation and refractory temporal lobe epilepsy. Epilepsia 42, 782-784. (Pubitemid 32605942)
-
(2001)
Epilepsia
, vol.42
, Issue.6
, pp. 782-784
-
-
Buono, R.J.1
Ferraro, T.N.2
O'Connor, M.J.3
Sperling, M.R.4
Ryan, S.G.5
Scattergood, T.6
Mulholland, N.7
Gilmore, J.8
Lohoff, F.W.9
Berrettini, W.H.10
-
14
-
-
23444437212
-
Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: Where to from here
-
DOI 10.1093/brain/awh524
-
Cavalleri, G.L., Lynch, J.M., Depondt, C., Burley, M.-W., Wood, N.W., Sisodiya, S.M., and Goldstein, D.B. (2005). Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here Brain 128, 1832-1840. (Pubitemid 41373654)
-
(2005)
Brain
, vol.128
, Issue.8
, pp. 1832-1840
-
-
Cavalleri, G.L.1
Lynch, J.M.2
Depondt, C.3
Burley, M.-W.4
Wood, N.W.5
Sisodiya, S.M.6
Goldstein, D.B.7
-
15
-
-
0034606323
-
Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor 4 subunit (CHRNA4) and IGE
-
Chioza, B., Goodwin, H., Blower, J., McCormick, D., Nashef, L., Asherson, P., and Makoff, A.J. (2000). Failure to replicate association between the gene for the neuronal nicotinic acetylcholine receptor 4 subunit (CHRNA4) and IGE. Am. J. Med. Genet. 96, 814-816.
-
(2000)
Am. J. Med. Genet.
, vol.96
, pp. 814-816
-
-
Chioza, B.1
Goodwin, H.2
Blower, J.3
McCormick, D.4
Nashef, L.5
Asherson, P.6
Makoff, A.J.7
-
16
-
-
0036891055
-
Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes
-
DOI 10.1016/S0920-1211(02)00195-X, PII S092012110200195X
-
Chioza, B., Osei-Lah, A., Wilkie, H., Nashef, L., McCormick, D., Asherson, P., and Makoff, A.J. (2002). Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes. Epilepsy Res. 52, 107-116. (Pubitemid 35379797)
-
(2002)
Epilepsy Research
, vol.52
, Issue.2
, pp. 107-116
-
-
Chioza, B.1
Osei-Lah, A.2
Wilkie, H.3
Nashef, L.4
McCormick, D.5
Asherson, P.6
Makoff, A.J.7
-
17
-
-
0035487324
-
Influenza A infection is an important cause of febrile seizures
-
Chiu, S.S., Tse, C.Y.C., Lau, Y.L., and Peiris, M. (2001). Influenza A infection is an important cause of febrile seizures. Pediatrics 108, e63.
-
(2001)
Pediatrics
, vol.108
-
-
Chiu, S.S.1
Tse, C.Y.C.2
Lau, Y.L.3
Peiris, M.4
-
18
-
-
10744228608
-
A Korean Kindred with Autosomal Dominant Nocturnal Frontal Lobe Epilepsy and Mental Retardation
-
DOI 10.1001/archneur.60.11.1625
-
Cho, Y., Motamedi, G.K., Laufenberg, I., Sohn, S.I., Lim, J.G., Lee, H., Yi, S.D., Lee, J.H., Kim, D.K., Reba, R., et al. (2003). A Korean kindred with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation. Arch. Neurol. 60, 1625-1632. (Pubitemid 37443131)
-
(2003)
Archives of Neurology
, vol.60
, Issue.11
, pp. 1625-1632
-
-
Cho, Y.-W.1
Motamedi, G.K.2
Laufenberg, I.3
Sohn, S.-I.4
Lim, J.-G.5
Lee, H.6
Yi, S.-D.7
Lee, J.-H.8
Kim, D.-K.9
Reba, R.10
Gaillard, W.D.11
Theodore, W.H.12
Lesser, R.P.13
Steinlein, O.K.14
-
19
-
-
84896743849
-
Single nucleotide polymorphisms of GABRG2 in febrile seizures and GEFS
-
Cho, S.M., Kim, Y.H., Chung, S.Y., Lee, I.G., Whang, K.T., Lee, B.C., and Lee, K.H. (2005). Single nucleotide polymorphisms of GABRG2 in febrile seizures and GEFS+. J. Korean Child Neurol. Soc. 13, 144-151.
-
(2005)
J. Korean Child Neurol. Soc.
, vol.13
, pp. 144-151
-
-
Cho, S.M.1
Kim, Y.H.2
Chung, S.Y.3
Lee, I.G.4
Whang, K.T.5
Lee, B.C.6
Lee, K.H.7
-
20
-
-
0037191355
-
The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions
-
Chou, I.C., Tsai, F.J., Huang, C.C., Lin, C.C., and Tsai, C.H. (2002). The voltage-gated potassium channel KCNQ2 in Taiwanese children with febrile convulsions. Neuroreport 13, 1971-1973. (Pubitemid 35398970)
-
(2002)
NeuroReport
, vol.13
, Issue.15
, pp. 1971-1973
-
-
Chou, I.-C.1
Tsai, F.-J.2
Huang, C.-C.3
Lin, C.C.4
Tsai, C.H.5
-
21
-
-
0042572286
-
Association of the neuronal nicotinic acetylcholine receptor subunit α4 polymorphisms with febrile convulsions
-
DOI 10.1046/j.1528-1157.2003.t01-1-44702.x
-
Chou, I.C., Lee, C.-C., Huang, C.-C., Wu, J.-Y., Tsai, J.J.P., Tsai, C.-H., and Tsai, F.-J. (2003a). Association of the neuronal nicotinic acetylcholine receptor subunit 4 polymorphisms with febrile convulsions. Epilepsia 44, 1089-1093. (Pubitemid 36959316)
-
(2003)
Epilepsia
, vol.44
, Issue.8
, pp. 1089-1093
-
-
Chou, I.-C.1
Lee, C.-C.2
Huang, C.-C.3
Wu, J.-Y.4
Tsai, J.J.P.5
Tsai, C.-H.6
Tsai, F.-J.7
-
22
-
-
0038648525
-
Association analysis of γ2 subunit of γ-aminobutyric acid type A receptor polymorphisms with febrile seizures
-
DOI 10.1203/01.PDR.0000069696.96041.34
-
Chou, I.C., Peng, C.T., Huang, C.C., Tsai, J.J., Tsai, F.J., and Tsai, C.H. (2003b). Association analysis of 2 subunit of -aminobutyric acid type A receptor polymorphisms with febrile seizures. Pediatr. Res. 54, 26-29. (Pubitemid 36736801)
-
(2003)
Pediatric Research
, vol.54
, Issue.1
, pp. 26-29
-
-
Chou, I.-C.1
Peng, C.-T.2
Huang, C.-C.3
Tsai, J.J.P.4
Tsai, F.-J.5
Tsai, C.-H.6
-
23
-
-
0038735544
-
The lack of association between febrile convulsions and polymorphisms in SCN1A
-
DOI 10.1016/S0920-1211(03)00043-3
-
Chou, I.C., Peng, C.-T., Tsai, F.-J., Huang, C.-C., Shi, Y.-R., and Tsai, C.-H. (2003c). The lack of association between febrile convulsions and polymorphisms in SCN1A. Epilepsy Res. 54, 53-57. (Pubitemid 36556198)
-
(2003)
Epilepsy Research
, vol.54
, Issue.1
, pp. 53-57
-
-
Chou, I.-C.1
Peng, C.-T.2
Tsai, F.-J.3
Huang, C.-C.4
Shi, Y.-R.5
Tsai, C.-H.6
-
24
-
-
0345257307
-
Association between polymorphism of interleukin-1-511 promoter and susceptibility to febrile convulsions in Taiwanese children
-
Chou, I.C., Tsai, C.H., Hsieh, Y.Y., Peng, C.T., and Tsai, F.J. (2003d). Association between polymorphism of interleukin-1-511 promoter and susceptibility to febrile convulsions in Taiwanese children. Acta Paediatr. 92, 1356.
-
(2003)
Acta Paediatr.
, vol.92
, pp. 1356
-
-
Chou, I.C.1
Tsai, C.H.2
Hsieh, Y.Y.3
Peng, C.T.4
Tsai, F.J.5
-
25
-
-
3242757396
-
Brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms in febrile seizures
-
DOI 10.1016/j.eplepsyres.2004.05.001, PII S0920121104000920
-
Chou, I.C., Tsai, C.-H., Lee, C.-C., Lin, S.-S., and Tsai, F.-J. (2004). Brain-derived neurotrophic factor (BDNF) Val66Met polymorphisms in febrile seizures. Epilepsy Res. 60, 27-29. (Pubitemid 38981758)
-
(2004)
Epilepsy Research
, vol.60
, Issue.1
, pp. 27-29
-
-
Chou, I.-C.1
Tsai, C.-H.2
Lee, C.-C.3
Lin, S.-S.4
Tsai, F.-J.5
-
26
-
-
33947224258
-
Association of GABRG2 Polymorphisms With Idiopathic Generalized Epilepsy
-
DOI 10.1016/j.pediatrneurol.2006.09.011, PII S088789940600573X
-
Chou, I.C., Lee, C.-C., Tsai, C.-H., Tsai, Y., Wan, L., Hsu, Y.-A., Li, T.C., and Tsai, F.J. (2007). Association of GABRG2 polymorphisms with idiopathic generalized epilepsy. Pediatr. Neurol. 36, 40-44. (Pubitemid 46427790)
-
(2007)
Pediatric Neurology
, vol.36
, Issue.1
, pp. 40-44
-
-
Chou, I.-C.1
Lee, C.-C.2
Tsai, C.-H.3
Tsai, Y.4
Wan, L.5
Hsu, Y.-A.6
Li, T.-C.7
Tsai, F.-J.8
-
27
-
-
77953488640
-
Interleukin (IL)-1, IL-1 receptor antagonist, IL-6, IL-8, IL-10, and tumor necrosis factor gene polymorphisms in patients with febrile seizures
-
Chou, I.C., Lin, W.-D., Wang, C.-H., Tsai, C.-H., Li, T.-C., and Tsai, F.-J. (2010). Interleukin (IL)-1, IL-1 receptor antagonist, IL-6, IL-8, IL-10, and tumor necrosis factor gene polymorphisms in patients with febrile seizures. J. Clin. Lab. Anal. 24, 154-159.
-
(2010)
J. Clin. Lab. Anal.
, vol.24
, pp. 154-159
-
-
Chou, I.C.1
Lin, W.-D.2
Wang, C.-H.3
Tsai, C.-H.4
Li, T.-C.5
Tsai, F.-J.6
-
28
-
-
84896747867
-
Interleukin-1beta promoter polymorphisms in febrile seizures and GEFS+
-
Chung, S.Y., Park, Y.J., Kim, Y.H., Lee, I.G., Whang, K.T., Lee, J.S., Kim, H.S., Lee, K.H., and Yim, S.V. (2006). Interleukin-1beta promoter polymorphisms in febrile seizures and GEFS+. J. Korean Child Neurol. Soc. 14, 113-120.
-
(2006)
J. Korean Child Neurol. Soc.
, vol.14
, pp. 113-120
-
-
Chung, S.Y.1
Park, Y.J.2
Kim, Y.H.3
Lee, I.G.4
Whang, K.T.5
Lee, J.S.6
Kim, H.S.7
Lee, K.H.8
Yim, S.V.9
-
29
-
-
0027170578
-
Guidelines for epidemiologic studies on epilepsy
-
Commission on Epidemiology and Prognosis, International League Against Epilepsy
-
Commission on Epidemiology and Prognosis, International League Against Epilepsy.(1993). Guidelines for epidemiologic studies on epilepsy. Epilepsia 34, 592-596.
-
(1993)
Epilepsia
, vol.34
, pp. 592-596
-
-
-
30
-
-
2442689512
-
Cytokines and fever
-
d1000-1499
-
Conti, B., Tabarean, I., Andrei, C., and Bartfai, T. (2004). Cytokines and fever. Front. Biosci. 9, 1433-1449. (Pubitemid 39066207)
-
(2004)
Frontiers in Bioscience
, vol.9
, pp. 1433-1449
-
-
Conti, B.1
Tabarean, I.2
Andrei, C.3
Bartfai, T.4
-
31
-
-
0025989275
-
The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins
-
Corey, L.A., Berg, K., Pellock, J.M., Solaas, M.H., Nance, W.E., and DeLorenzo, R.J. (1991). The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins. Neurology 41, 1433.
-
(1991)
Neurology
, vol.41
, pp. 1433
-
-
Corey, L.A.1
Berg, K.2
Pellock, J.M.3
Solaas, M.H.4
Nance, W.E.5
Delorenzo, R.J.6
-
32
-
-
84865773659
-
Fever and fever-related epilepsies
-
Cross, J.H. (2012). Fever and fever-related epilepsies. Epilepsia 53, 3-8.
-
(2012)
Epilepsia
, vol.53
, pp. 3-8
-
-
Cross, J.H.1
-
33
-
-
55749108511
-
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33
-
Dai, X.-H., Chen, W.-W., Wang, X., Zhu, Q.-H., Li, C., Li, L., Liu, M.G., Wang, Q.K., and Liu, J.Y. (2008). A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33. Hum. Genet. 124, 423-429.
-
(2008)
Hum. Genet.
, vol.124
, pp. 423-429
-
-
Dai, X.-H.1
Chen, W.-W.2
Wang, X.3
Zhu, Q.-H.4
Li, C.5
Li, L.6
Liu, M.G.7
Wang, Q.K.8
Liu, J.Y.9
-
34
-
-
77951728544
-
Augmented currents of an HCN2 variant in patients with febrile seizure syndromes
-
Dibbens, L.M., Reid, C.A., Hodgson, B., Thomas, E.A., Phillips, A.M., Gazina, E., Cromer, B.A., Clarke, A.L., Baram, T.Z., Scheffer, I.E., et al. (2010). Augmented currents of an HCN2 variant in patients with febrile seizure syndromes. Ann. Neurol. 67, 542-546.
-
(2010)
Ann. Neurol.
, vol.67
, pp. 542-546
-
-
Dibbens, L.M.1
Reid, C.A.2
Hodgson, B.3
Thomas, E.A.4
Phillips, A.M.5
Gazina, E.6
Cromer, B.A.7
Clarke, A.L.8
Baram, T.Z.9
Scheffer, I.E.10
-
35
-
-
11144237593
-
Interleukin-1β contributes to the generation of experimental febrile seizures
-
DOI 10.1002/ana.20358
-
Dubé, C., Vezzani, A., Behrens, M., Bartfai, T., and Baram, T.Z. (2005). Interleukin-1β contributes to the generation of experimental febrile seizures. Ann. Neurol. 57, 152-155. (Pubitemid 40053330)
-
(2005)
Annals of Neurology
, vol.57
, Issue.1
, pp. 152-155
-
-
Dube, C.1
Vezzani, A.2
Behrens, M.3
Bartfai, T.4
Baram, T.Z.5
-
36
-
-
0024409405
-
Effect of fever on recurrence rate of febrile convulsions
-
el-Radhi, A.S. and Banajeh, S. (1989). Effect of fever on recurrence rate of febrile convulsions. Arch. Dis. Child. 64, 869-870.
-
(1989)
Arch. Dis. Child.
, vol.64
, pp. 869-870
-
-
El-Radhi, A.S.1
Banajeh, S.2
-
37
-
-
0035071143
-
A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus - And prevalence of variants in patients with epilepsy
-
DOI 10.1086/319524
-
Escayg, A., Heils, A., MacDonald, B.T., Haug, K., Sander, T., and Meisler, M.H. (2001). A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus-and prevalence of variants in patients with epilepsy. Am. J. Hum. Genet. 68, 866-873. (Pubitemid 32289732)
-
(2001)
American Journal of Human Genetics
, vol.68
, Issue.4
, pp. 866-873
-
-
Escayg, A.1
Heils, A.2
Macdonald, B.T.3
Haug, K.4
Sander, T.5
Meisler, M.H.6
-
38
-
-
36348984471
-
Assessment of febrile seizures in children
-
DOI 10.1007/s00431-007-0577-x
-
Fetveit, A. (2008). Assessment of febrile seizures in children. Eur. J. Pediatr. 167, 17-27. (Pubitemid 350159829)
-
(2008)
European Journal of Pediatrics
, vol.167
, Issue.1
, pp. 17-27
-
-
Fetveit, A.1
-
39
-
-
77957019872
-
Association of apolipoprotein e polymorphisms with temporal lobe epilepsy in a Chinese Han population
-
Fu, Y.-H., Lv, R.-J., Jin, L.-R., Lu, Q., Shao, X.-Q., He, J.-S., Wu, L.W., Zhang, L.S., and Hu, H.G. (2010). Association of apolipoprotein E polymorphisms with temporal lobe epilepsy in a Chinese Han population. Epilepsy Res. 91, 253-259.
-
(2010)
Epilepsy Res.
, vol.91
, pp. 253-259
-
-
Fu, Y.-H.1
Lv, R.-J.2
Jin, L.-R.3
Lu, Q.4
Shao, X.-Q.5
He, J.-S.6
Wu, L.W.7
Zhang, L.S.8
Hu, H.G.9
-
40
-
-
84896774559
-
A study on the association of polymorphism of IL-10 with febrile convulsion
-
Gao, B., Hu, M.-s., and Zhang, L. (2007). A study on the association of polymorphism of IL-10 with febrile convulsion. Chin. J. Birth Health Hered. 3, 009.
-
(2007)
Chin. J. Birth Health Hered.
, vol.3
, pp. 009
-
-
Gao, B.1
Hu, M.-S.2
Zhang, L.3
-
41
-
-
84896762411
-
Association between polymorphism of exon 7-21C > T in SCN1A and generalized epilepsy with febrile seizures plus patients
-
Gao, M.-m., Qin, B., Shi, Y.-w., Yu, M.-j., Deng, W.-y., and Liao, W.-p. (2010). Association between polymorphism of exon 7-21C > T in SCN1A and generalized epilepsy with febrile seizures plus patients. J. Trop. Med. 5, 027.
-
(2010)
J. Trop. Med.
, vol.5
, pp. 027
-
-
Gao, M.-M.1
Qin, B.2
Shi, Y.-W.3
Yu, M.-J.4
Deng, W.-Y.5
Liao, W.-P.6
-
42
-
-
52049087355
-
Role of apolipoprotein e in febrile convulsion
-
Giray, Ö., Ülgenalp, A., Bora, E., Uran, N., Yilmaz, E., Ünalp, A., and Erçal, D. (2008). Role of apolipoprotein E in febrile convulsion. Pediatr. Neurol. 39, 241-244.
-
(2008)
Pediatr. Neurol.
, vol.39
, pp. 241-244
-
-
Giray, Ö.1
Ülgenalp, A.2
Bora, E.3
Uran, N.4
Yilmaz, E.5
Ünalp, A.6
Erçal, D.7
-
43
-
-
84872189159
-
Lack of association between rs211037 of the GABRG2 gene and juvenile myoclonic epilepsy in Brazilian population
-
Gitaí, L., de Almeida, D., Born, J., Gameleira, F., de Andrade, T., Machado, L., and Gitaí, D.L. (2012). Lack of association between rs211037 of the GABRG2 gene and juvenile myoclonic epilepsy in Brazilian population. Neurol. India 60, 585.
-
(2012)
Neurol. India
, vol.60
, pp. 585
-
-
Gitaí, L.1
De Almeida, D.2
Born, J.3
Gameleira, F.4
De Andrade, T.5
MacHado, L.6
Gitaí, D.L.7
-
44
-
-
27744517989
-
Lack of an association between candidate gene loci and idiopathic generalized epilepsy in Kuwaiti Arab children
-
DOI 10.1007/s11373-005-9009-y
-
Haider, M.Z., Habeeb, Y., Al-Nakkas, E., Al-Anzi, H., Zaki, M., Al-Tawari, A., and Al-Bloushi, M. (2005). Lack of an association between candidate gene loci and idiopathic generalized epilepsy in Kuwaiti Arab children. J. Biomed. Sci. 12, 815-818. (Pubitemid 41625947)
-
(2005)
Journal of Biomedical Science
, vol.12
, Issue.5
, pp. 815-818
-
-
Haider, M.Z.1
Habeeb, Y.2
Al-Nakkas, E.3
Al-Anzi, H.4
Zaki, M.5
Al-Tawari, A.6
Al-Bloushi, M.7
-
45
-
-
0028071131
-
Human herpes virus-6 infection in children: A prospective study of complications and reactivatio
-
Hall, C.B., Long, C.E., Schnabel, K.C., Caserta, M.T., McIntyre, K.M., Costanzo, M.A., Knott, A., Dewhurst, S., Insel, R.A., and Epstein, L.G. (1994). Human herpes virus-6 infection in children: a prospective study of complications and reactivation. N. Engl. J. Med. 331, 432-438.
-
(1994)
N. Engl. J. Med.
, vol.331
, pp. 432-438
-
-
Hall, C.B.1
Long, C.E.2
Schnabel, K.C.3
Caserta, M.T.4
McIntyre, K.M.5
Costanzo, M.A.6
Knott, A.7
Dewhurst, S.8
Insel, R.A.9
Epstein, L.G.10
-
46
-
-
0031948473
-
Epilepsy diagnosis and localization in patients with antecedent childhood febrile convulsions
-
Hamati-Haddad, A. and Abou-Khalil, B. (1998). Epilepsy diagnosis and localization in patients with antecedent childhood febrile convulsions. Neurology 50, 917-922. (Pubitemid 28212815)
-
(1998)
Neurology
, vol.50
, Issue.4
, pp. 917-922
-
-
Hamati-Haddad, A.1
Abou-Khalil, B.2
-
47
-
-
0036772091
-
Interleukin-1β, tumor necrosis factor-α, and nitrite levels in febrile seizures
-
Haspolat, S., Mihçi, E., Cokun, M., Gümüslü, S., Özbenm, T., and Yegin, O. (2002). Interleukin-1β, tumor necrosis factor-α, and nitrite levels in febrile seizures. J. Child Neurol. 17, 749-751. (Pubitemid 36163687)
-
(2002)
Journal of Child Neurology
, vol.17
, Issue.10
, pp. 749-751
-
-
Haspolat, S.1
Mihci, E.2
Coskun, M.3
Gumuslu, S.4
Ozbenm, T.5
Yegin, O.6
-
48
-
-
24344435545
-
Interleukin-1α, interleukin-1β, and interleukin-1Ra polymorphisms in febrile seizures
-
Haspolat, ., Baysal, Y., Duman, Ö., Cokun, M., Tosun, Ö., and Yein, O. (2005). Interleukin-1α, interleukin-1β, and interleukin-1Ra polymorphisms in febrile seizures. J. Child Neurol. 20, 565-568. (Pubitemid 41245796)
-
(2005)
Journal of Child Neurology
, vol.20
, Issue.7
, pp. 565-568
-
-
Haspolat, S.1
Baysal, Y.2
Duman, O.3
Coskun, M.4
Tosun, O.5
Yegin, O.6
-
49
-
-
0035656999
-
The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy
-
DOI 10.1016/S0920-1211(01)00312-6, PII S0920121101003126
-
Haug, K., Hallmann, K., Rebstock, J., Dullinger, J., Muth, S., Haverkamp, F., Pfeiffer, H., Rau, B., Elger, C.E., Propping, P., et al. (2001). The voltage-gated sodium channel gene SCN2A and idiopathic generalized epilepsy. Epilepsy Res. 47, 243-246. (Pubitemid 34008467)
-
(2001)
Epilepsy Research
, vol.47
, Issue.3
, pp. 243-246
-
-
Haug, K.1
Hallmann, K.2
Rebstock, J.3
Dullinger, J.4
Muth, S.5
Haverkamp, F.6
Pfeiffer, H.7
Rau, B.8
Elger, C.E.9
Propping, P.10
Heils, A.11
-
50
-
-
33749684849
-
Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22
-
DOI 10.1111/j.1528-1167.2006.00637.x
-
Hedera, P., Ma, S., Blair, M.A., Taylor, K.A., Hamati, A., Bradford, Y., Abou-Khalil, B., and Haines, J.L. (2006). Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22. Epilepsia 47, 1622-1628. (Pubitemid 44556395)
-
(2006)
Epilepsia
, vol.47
, Issue.10
, pp. 1622-1628
-
-
Hedera, P.1
Ma, S.2
Blair, M.A.3
Taylor, K.A.4
Hamati, A.5
Bradford, Y.6
Abou-Khalil, B.7
Haines, J.L.8
-
51
-
-
33644794932
-
Causal links between brain cytokines and experimental febrile convulsions in the rat
-
DOI 10.1111/j.1528-1167.2005.00294.x
-
Heida, J.G. and Pittman, Q.J. (2005). Causal links between brain cytokines and experimental febrile convulsions in the rat. Epilepsia 46, 1906-1913. (Pubitemid 44922001)
-
(2005)
Epilepsia
, vol.46
, Issue.12
, pp. 1906-1913
-
-
Heida, J.G.1
Pittman, Q.J.2
-
52
-
-
64649085803
-
The role of interleukin-1β in febrile seizures
-
Heida, J.G., Moshé, S.L., and Pittman, Q.J. (2009). The role of interleukin-1β in febrile seizures. Brain Dev. 31, 388-393.
-
(2009)
Brain Dev.
, vol.31
, pp. 388-393
-
-
Heida, J.G.1
Moshé, S.L.2
Pittman, Q.J.3
-
53
-
-
84866091152
-
Design and phenomenology of the FEBSTAT study
-
Hesdorffer, D.C., Shinnar, S., Lewis, D.V., Moshé, S.L., Nordli, D.R., Pellock, J.M., MacFall, J., Shinnar, R.C., Masur, D., Frank, L.M., et al. (2012). Design and phenomenology of the FEBSTAT study. Epilepsia 53, 1471-1480.
-
(2012)
Epilepsia
, vol.53
, pp. 1471-1480
-
-
Hesdorffer, D.C.1
Shinnar, S.2
Lewis, D.V.3
Moshé, S.L.4
Nordli, D.R.5
Pellock, J.M.6
MacFall, J.7
Shinnar, R.C.8
Masur, D.9
Frank, L.M.10
-
54
-
-
77955341050
-
Temporal Lobe epilepsy and matrix metalloproteinase 9: A tempting relation but negative genetic association
-
Heuser, K., Hoddevik, E.H., Taubøll, E., Gjerstad, L., Indahl, U., Kaczmarek, L., Berg, P.R., Lien, S., Nagelhus, E.A., and Ottersen, O.P. (2010a). Temporal Lobe epilepsy and matrix metalloproteinase 9: a tempting relation but negative genetic association. Seizure 19, 335-338.
-
(2010)
Seizure
, vol.19
, pp. 335-338
-
-
Heuser, K.1
Hoddevik, E.H.2
Taubøll, E.3
Gjerstad, L.4
Indahl, U.5
Kaczmarek, L.6
Berg, P.R.7
Lien, S.8
Nagelhus, E.A.9
Ottersen, O.P.10
-
55
-
-
72549112818
-
Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy
-
Heuser, K., Nagelhus, E.A., Taubøll, E., Indahl, U., Berg, P.R., Lien, S., Nakken, S., Gjerstad, L., and Ottersen, O.P. (2010b). Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy. Epilepsy Res. 88, 55-64.
-
(2010)
Epilepsy Res.
, vol.88
, pp. 55-64
-
-
Heuser, K.1
Nagelhus, E.A.2
Taubøll, E.3
Indahl, U.4
Berg, P.R.5
Lien, S.6
Nakken, S.7
Gjerstad, L.8
Ottersen, O.P.9
-
56
-
-
0033544326
-
A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy
-
Hirose, S., Iwata, H., Akiyoshi, H., Kobayashi, K., Ito, M., Wada, K., Kaneko, S., and Mitsudome, A. (1999). A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy. Neurology 53, 1749-1753. (Pubitemid 29530350)
-
(1999)
Neurology
, vol.53
, Issue.8
, pp. 1749-1753
-
-
Hirose, S.1
Iwata, H.2
Akiyoshi, H.3
Kobayashi, K.4
Ito, M.5
Wada, K.6
Kaneko, S.7
Mitsudome, A.8
-
57
-
-
84876915067
-
SCN1A testing for epilepsy: Application in clinical practice
-
Hirose, S., Scheffer, I.E., Marini, C., De Jonghe, P., Andermann, E., Goldman, A.M., Kauffman, M., Tan, N.C., Lowenstein, D.H., Sisodiya, S.M., et al. (2013). SCN1A testing for epilepsy: application in clinical practice. Epilepsia 54, 946-952.
-
(2013)
Epilepsia
, vol.54
, pp. 946-952
-
-
Hirose, S.1
Scheffer, I.E.2
Marini, C.3
De Jonghe, P.4
Andermann, E.5
Goldman, A.M.6
Kauffman, M.7
Tan, N.C.8
Lowenstein, D.H.9
Sisodiya, S.M.10
-
58
-
-
0033014962
-
Risk factors for a first febrile convulsion in children: A population study in southern Taiwan
-
DOI 10.1111/j.1528-1157.1999.tb00769.x
-
Huang, C.-C., Wang, S.-T., Chang, Y.-C., Huang, M.-C., Chi, Y.-C., and Tsai, J.-J. (1999). Risk factors for a first febrile convulsion in children: a population study in Southern Taiwan. Epilepsia 40, 719-725. (Pubitemid 29260710)
-
(1999)
Epilepsia
, vol.40
, Issue.6
, pp. 719-725
-
-
Huang, C.-C.1
Wang, S.-T.2
Chang, Y.-C.3
Huang, M.-C.4
Chi, Y.-C.5
Tsai, J.-J.6
-
59
-
-
63849160979
-
Interleukin-10 is associated with resistance to febrile seizures: Genetic association and experimental animal studies
-
Ishizaki, Y., Kira, R., Fukuda, M., Torisu, H., Sakai, Y., Sanefuji, M., Yukaya, N., and Hara, T. (2009). Interleukin-10 is associated with resistance to febrile seizures: genetic association and experimental animal studies. Epilepsia 50, 761-767.
-
(2009)
Epilepsia
, vol.50
, pp. 761-767
-
-
Ishizaki, Y.1
Kira, R.2
Fukuda, M.3
Torisu, H.4
Sakai, Y.5
Sanefuji, M.6
Yukaya, N.7
Hara, T.8
-
60
-
-
77958550127
-
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures
-
Jamali, S., Salzmann, A., Perroud, N., Ponsole-Lenfant, M., Cillario, J., Roll, P., Roeckel-Trevisiol, N., Crespel, A., Balzar, J., Schlachter, K., et al. (2010). Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures. PloS One 5, e12740.
-
(2010)
PloS One
, vol.5
-
-
Jamali, S.1
Salzmann, A.2
Perroud, N.3
Ponsole-Lenfant, M.4
Cillario, J.5
Roll, P.6
Roeckel-Trevisiol, N.7
Crespel, A.8
Balzar, J.9
Schlachter, K.10
-
61
-
-
84871719298
-
-
Oxford University Press
-
Jasper, H.H., Noebels, J.L., Noebels, J., Avoli, M., Rogawski, M., and Olsen, R. (2012). Jasper's Basic Mechanisms of the Epilepsies (Oxford University Press).
-
(2012)
Jasper's Basic Mechanisms of the Epilepsies
-
-
Jasper, H.H.1
Noebels, J.L.2
Noebels, J.3
Avoli, M.4
Rogawski, M.5
Olsen, R.6
-
62
-
-
0142104320
-
Association Analysis of a Polymorphism of Interleukin 1β (IL-1β) Gene with Temporal Lobe Epilepsy in a Chinese Population
-
DOI 10.1046/j.1528-1157.2003.11003.x
-
Jin, L., Jia, Y., Zhang, B., Xu, Q., Fan, Y., Wu, L., Shen, Y. (2003). Association analysis of a polymorphism of interleukin 1(IL-1) gene with temporal lobe epilepsy in a Chinese population. Epilepsia 44, 1306-1309. (Pubitemid 37280375)
-
(2003)
Epilepsia
, vol.44
, Issue.10
, pp. 1306-1309
-
-
Jin, L.1
Jia, Y.2
Zhang, B.3
Xu, Q.4
Fan, Y.5
Wu, L.6
Shen, Y.7
-
63
-
-
6844240853
-
Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest
-
DOI 10.1093/hmg/7.1.63
-
Johnson, E.W., Dubovsky, J., Rich, S.S., O'Donovan, C.A., Orr, H.T., Anderson, V.E., Gil-Nagel, A., Ahmann, P., Dokken, C.G., Schneider, D.T., et al. (1998). Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest. Hum. Mol. Gen. 7, 63-67. (Pubitemid 28040738)
-
(1998)
Human Molecular Genetics
, vol.7
, Issue.1
, 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
Gil-Nagel, A.7
Ahmann, P.8
Dokken, C.G.9
Schneider, D.T.10
Weber, J.L.11
-
64
-
-
0036318060
-
A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions
-
DOI 10.1001/archneur.59.7.1137
-
Kananura, C., Haug, K., Sander, T., Runge, U., Gu, W., Hallmann, K., Rebstock, J., Heils, A., and Steinlein, O.K. (2002). A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions. Arch. Neurol. 59, 1137-1141. (Pubitemid 34755827)
-
(2002)
Archives of Neurology
, vol.59
, Issue.7
, pp. 1137-1141
-
-
Kananura, C.1
Haug, K.2
Sander, T.3
Runge, U.4
Gu, W.5
Hallmann, K.6
Rebstock, J.7
Heils, A.8
Steinlein, O.K.9
-
65
-
-
0033625146
-
Interleukin (IL)-1β, IL-1α, and IL-1 receptor antagonist gene polymorphisms in patients with temporal lobe epilepsy
-
DOI 10.1002/1531-8249(200005)47:5<571::AID-ANA3>3.0.CO;2-A
-
Kanemoto, K., Kawasaki, J., Miyamoto, T., Obayashi, H., and Nishimura, M. (2000). Interleukin (IL)-1, IL-1, and IL-1 receptor antagonist gene polymorphisms in patients with temporal lobe epilepsy. Ann. Neurol. 47, 571-574. (Pubitemid 30261891)
-
(2000)
Annals of Neurology
, vol.47
, Issue.5
, pp. 571-574
-
-
Kanemoto, K.1
Kawasaki, J.2
Miyamoto, T.3
Obayashi, H.4
Nishimura, M.5
-
66
-
-
0347298828
-
Association of partial epilepsy with brain-derived neurotrophic factor (BDNF) gene polymorphisms
-
DOI 10.1016/S0920-1211(03)00032-9
-
Kanemoto, K., Kawasaki, J., Tarao, Y., Kumaki, T., Oshima, T., Kaji, R., and Nishimura, M. (2003a). Association of partial epilepsy with brain-derived neurotrophic factor (BDNF) gene polymorphisms. Epilepsy Res. 53, 255-258. (Pubitemid 36419620)
-
(2003)
Epilepsy Research
, vol.53
, Issue.3
, pp. 255-258
-
-
Kanemoto, K.1
Kawasaki, J.2
Tarao, Y.3
Kumaki, T.4
Oshima, T.5
Kaji, R.6
Nishimura, M.7
-
67
-
-
0038644567
-
Increased frequency of interleukin-1β-511T allele in patients with temporal lobe epilepsy, hippocampal sclerosis, and prolonged febrile convulsion
-
DOI 10.1046/j.1528-1157.2003.43302.x
-
Kanemoto, K., Kawasaki, J., Yuasa, S., Kumaki, T., Tomohiro, O., Kaji, R., and Nishimura, M. (2003b). Increased frequency of interleukin-1-511T allele in patients with temporal lobe epilepsy, hippocampal sclerosis, and prolonged febrile convulsion. Epilepsia 44, 796-799. (Pubitemid 36754004)
-
(2003)
Epilepsia
, vol.44
, Issue.6
, pp. 796-799
-
-
Kanemoto, K.1
Kawasaki, J.2
Yuasa, S.3
Kumaki, T.4
Tomohiro, O.5
Kaji, R.6
Nishimura, M.7
-
68
-
-
0141835899
-
Systemic cytokine responses in patients with influenza-associated encephalopathy
-
DOI 10.1086/377101
-
Kawada, J.-i., Kimura, H., Ito, Y., Hara, S., Iriyama, M., Yoshikawa, T., and Morishima, T. (2003). Systemic cytokine responses in patients with influenza-associated encephalopathy. J. Infect. Dis. 188, 690-698. (Pubitemid 37115182)
-
(2003)
Journal of Infectious Diseases
, vol.188
, Issue.5
, pp. 690-698
-
-
Kawada, J.-I.1
Kimura, H.2
Ito, Y.3
Hara, S.4
Iriyama, M.5
Yoshikawa, T.6
Morishima, T.7
-
69
-
-
84896785811
-
Lack of association between TNF-gene polymorphisms at position-308 A,-850T and risk of simple febrile convulsion in pediatric patients
-
Khoshdel, A., Kheiri, S., Habibian, R., Nozari, A., and Baradaran, A. (2012). Lack of association between TNF-gene polymorphisms at position-308 A,-850T and risk of simple febrile convulsion in pediatric patients. Adv. Biomed. Res. 1, 85.
-
(2012)
Adv. Biomed. Res.
, vol.1
, pp. 85
-
-
Khoshdel, A.1
Kheiri, S.2
Habibian, R.3
Nozari, A.4
Baradaran, A.5
-
70
-
-
84896765110
-
Brain-derived neurotrophic factor (BDNF) SNP 6265 polymorphisms in febrile seizure and GEFS+
-
Kim, S.E., Kim, H.G., Kim, Y.H., Choi, B.J., Hwang, H.S., Bin, J.H., Chung, S.Y., and Lee, I.G. (2008). Brain-derived neurotrophic factor (BDNF) SNP 6265 polymorphisms in febrile seizure and GEFS+. J. Korean Child Neurol. Soc. 16, 114-120.
-
(2008)
J. Korean Child Neurol. Soc.
, vol.16
, pp. 114-120
-
-
Kim, S.E.1
Kim, H.G.2
Kim, Y.H.3
Choi, B.J.4
Hwang, H.S.5
Bin, J.H.6
Chung, S.Y.7
Lee, I.G.8
-
71
-
-
84872222070
-
Mutation screening of the -aminobutyric acid type-A receptor subunit 2 gene in Korean patients with childhood absence epilepsy
-
Kim, Y.O., Kim, M.-K., Nam, T.-S., Jang, S.Y., Park, K.W., Kim, E.Y., Rho, Y.I., and Woo, Y.J. (2012). Mutation screening of the -aminobutyric acid type-A receptor subunit 2 gene in Korean patients with childhood absence epilepsy. J. Clin. Neurol. 8, 271-275.
-
(2012)
J. Clin. Neurol.
, vol.8
, pp. 271-275
-
-
Kim, Y.O.1
Kim, M.-K.2
Nam, T.-S.3
Jang, S.Y.4
Park, K.W.5
Kim, E.Y.6
Rho, Y.I.7
Woo, Y.J.8
-
72
-
-
33746934227
-
A receptor in epilepsy using tagging SNPs
-
DOI 10.1016/j.eplepsyres.2006.05.009, PII S0920121106001471
-
Kinirons, P., Cavalleri, G.L., Shahwan, A., Wood, N.W., Goldstein, D.B., Sisodiya, S.M., Delanty N., and Doherty, C.P. (2006). Examining the role of common genetic variation in the 2 subunit of the GABAA receptor in epilepsy using tagging SNPs. Epilepsy Res. 70, 229-238. (Pubitemid 44189186)
-
(2006)
Epilepsy Research
, vol.70
, Issue.2-3
, pp. 229-238
-
-
Kinirons, P.1
Cavalleri, G.L.2
Shahwan, A.3
Wood, N.W.4
Goldstein, D.B.5
Sisodiya, S.M.6
Delanty, N.7
Doherty, C.P.8
-
73
-
-
20644438439
-
Genetic susceptibility to simple febrile seizures: Interleukin-1β promoter polymorphisms are associated with sporadic cases
-
DOI 10.1016/j.neulet.2005.04.097, PII S0304394005005045
-
Kira, R., Torisu, H., Takemoto, M., Nomura, A., Sakai, Y., Sanefuji, M., Sakamoto, K., Matsumoto, S., Gondo, K., and Hara, T. (2005). Genetic susceptibility to simple febrile seizures: interleukin-1 promoter polymorphisms are associated with sporadic cases. Neurosci. Lett. 384, 239-244. (Pubitemid 40836007)
-
(2005)
Neuroscience Letters
, vol.384
, Issue.3
, pp. 239-244
-
-
Kira, R.1
Torisu, H.2
Takemoto, M.3
Nomura, A.4
Sakai, Y.5
Sanefuji, M.6
Sakamoto, K.7
Matsumoto, S.8
Gondo, K.9
Hara, T.10
-
74
-
-
71849094963
-
Genetic susceptibility to febrile seizures: Case-control association studies
-
Kira, R., Ishizaki, Y., Torisu, H., Sanefuji, M., Takemoto, M., Sakamoto, K., Matsumoto, S., Yamaguchi, Y., Yukaya, N., Sakai, Y., et al. (2010). Genetic susceptibility to febrile seizures: case-control association studies. Brain Dev. 32, 57-63.
-
(2010)
Brain Dev.
, vol.32
, pp. 57-63
-
-
Kira, R.1
Ishizaki, Y.2
Torisu, H.3
Sanefuji, M.4
Takemoto, M.5
Sakamoto, K.6
Matsumoto, S.7
Yamaguchi, Y.8
Yukaya, N.9
Sakai, Y.10
-
75
-
-
0036752812
-
Genetic and environmental factors in febrile seizures: A Danish population-based twin study
-
DOI 10.1016/S0920-1211(02)00121-3, PII S0920121102001213
-
Kjeldsen, M.J., Kyvik, K.O., Friis, M.L., and Christensen, K. (2002). Genetic and environmental factors in febrile seizures: a Danish population-based twin study. Epilepsy Res. 51, 167-177. (Pubitemid 35283887)
-
(2002)
Epilepsy Research
, vol.51
, Issue.1-2
, pp. 167-177
-
-
Kjeldsen, M.J.1
Kyvik, K.O.2
Friis, M.L.3
Christensen, K.4
-
76
-
-
17844366327
-
Genetic factors in seizures: A population-based study of 47,626 US, Norwegian and Danish twin pairs
-
DOI 10.1375/1832427053738836
-
Kjeldsen, M.J., Corey, L.A., Solaas, M.H., Friis, M.L., Harris, J.R., Kyvik, K.O., Christensen, K., and Pellock, J.M. (2005). Genetic factors in seizures: a population-based study of 47,626 US, Norwegian and Danish twin pairs. Twin Res. Hum. Genet. 8, 138-147. (Pubitemid 40593395)
-
(2005)
Twin Research and Human Genetics
, vol.8
, Issue.2
, pp. 138-147
-
-
Kjeldsen, M.J.1
Corey, L.A.2
Solaas, M.H.3
Friis, M.L.4
Harris, J.R.5
Kyvik, K.O.6
Christensen, K.7
Pellock, J.M.8
-
77
-
-
0025960495
-
Fever: Role of pyrogens and cryogens
-
Kluger, M.J. (1991). Fever: role of pyrogens and cryogens. Physiol. Rev. 71, 93-127.
-
(1991)
Physiol. Rev.
, vol.71
, pp. 93-127
-
-
Kluger, M.J.1
-
78
-
-
0022382798
-
Recurrence risk after first febrile seizure and effect of short term diazepam prophylaxi
-
Knudsen, F.U. (1985). Recurrence risk after first febrile seizure and effect of short term diazepam prophylaxis. Arch. Dis. Child. 60, 1045-1049.
-
(1985)
Arch. Dis. Child.
, vol.60
, pp. 1045-1049
-
-
Knudsen, F.U.1
-
79
-
-
77950594101
-
Association of subunit of GABAA receptor subtype gene polymorphisms with epilepsy susceptibility and drug resistance in north Indian population
-
Kumari, R., Lakhan, R., Kalita, J., Misra, U.K., and Mittal, B. (2010). Association of subunit of GABAA receptor subtype gene polymorphisms with epilepsy susceptibility and drug resistance in north Indian population. Seizure 19, 237-241.
-
(2010)
Seizure
, vol.19
, pp. 237-241
-
-
Kumari, R.1
Lakhan, R.2
Kalita, J.3
Misra, U.K.4
Mittal, B.5
-
80
-
-
68449100608
-
Differential role of sodium channels SCN1A and SCN2A gene polymorphisms with epilepsy and multiple drug resistance in the north Indian population
-
Lakhan, R., Kumari, R., Misra, U.K., Kalita, J., Pradhan, S., and Mittal, B. (2009). Differential role of sodium channels SCN1A and SCN2A gene polymorphisms with epilepsy and multiple drug resistance in the north Indian population. Br. J. Clin. Pharmacol. 68, 214-220.
-
(2009)
Br. J. Clin. Pharmacol.
, vol.68
, pp. 214-220
-
-
Lakhan, R.1
Kumari, R.2
Misra, U.K.3
Kalita, J.4
Pradhan, S.5
Mittal, B.6
-
81
-
-
80053562342
-
Replication of association between a SCN1A splice variant and febrile seizures
-
Le Gal, F., Salzmann, A., Crespel, A., and Malafosse, A. (2011). Replication of association between a SCN1A splice variant and febrile seizures. Epilepsia 52, e135-e138.
-
(2011)
Epilepsia
, vol.52
-
-
Le Gal, F.1
Salzmann, A.2
Crespel, A.3
Malafosse, A.4
-
82
-
-
0034100615
-
A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family
-
DOI 10.1055/s-2000-15290
-
Lee, W.L., Biervert, C., Hallmann, K., Tay, A., Dean, J.C., and Steinlein, O.K. (2000). A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family. Neuropediatrics 31, 9-12. (Pubitemid 30172979)
-
(2000)
Neuropediatrics
, vol.31
, Issue.1
, pp. 9-12
-
-
Lee, W.L.1
Biervert, C.2
Hallmann, K.3
Tay, A.4
Dean, J.C.S.5
Steinlein, O.K.6
-
83
-
-
34047210359
-
Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits
-
DOI 10.1002/jcla.20155
-
Lee, C.-C., Chou, I.C., Tsai, C.-H., Wan, L., Shu, Y.-A., Tsai, Y., Li, T.C., and Tsai, F.J. (2007). Association of idiopathic generalized epilepsy with polymorphisms in the neuronal nicotinic acetylcholine receptor subunits. J. Clin. Lab. Anal. 21, 67-70. (Pubitemid 46536876)
-
(2007)
Journal of Clinical Laboratory Analysis
, vol.21
, Issue.2
, pp. 67-70
-
-
Lee, C.-C.1
Chou, I.-C.2
Tsai, C.-H.3
Wan, L.4
Shu, Y.-A.5
Tsai, Y.6
Li, T.-C.7
Tsai, F.-J.8
-
84
-
-
0038491560
-
A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy
-
DOI 10.1046/j.1528-1157.2003.61102.x
-
Leniger, T., Kananura, C., Hufnagel, A., Bertrand, S., Bertrand, D., and Steinlein, O.K. (2003). A new Chrna4 mutation with low penetrance in nocturnal frontal lobe epilepsy. Epilepsia 44, 981-985. (Pubitemid 36842192)
-
(2003)
Epilepsia
, vol.44
, Issue.7
, pp. 981-985
-
-
Leniger, T.1
Kananura, C.2
Hufnagel, A.3
Bertrand, S.4
Bertrand, D.5
Steinlein, O.K.6
-
85
-
-
37149042571
-
Neuropeptide y gene polymorphism and plasma neuropeptide y level in febrile seizure patients in Taiwan
-
Lin, L.C., Lin, H.S., and Yang, R.C. (2007). Neuropeptide Y gene polymorphism and plasma neuropeptide Y level in febrile seizure patients in Taiwan. Kaohsiung J. Med. Sci. 23, 560-565.
-
(2007)
Kaohsiung J. Med. Sci.
, vol.23
, pp. 560-565
-
-
Lin, L.C.1
Lin, H.S.2
Yang, R.C.3
-
86
-
-
25844456860
-
Lack of association between variations in the brain-derived neurotrophic factor (BDNF) gene and temporal lobe epilepsy
-
DOI 10.1016/j.eplepsyres.2005.06.005, PII S092012110500135X
-
Lohoff, F.W., Ferraro, T.N., Dahl, J.P., Hildebrandt, M.A., Scattergood, T.M., O'Connor, M.J., Sperling, M.R., Dlugos, D.J., Berrettini, W.H., and Buono RJ. (2005). Lack of association between variations in the brain-derived neurotrophic factor (BDNF) gene and temporal lobe epilepsy. Epilepsy Res. 66, 59-62. (Pubitemid 41393943)
-
(2005)
Epilepsy Research
, vol.66
, Issue.1-3
, pp. 59-62
-
-
Lohoff, F.W.1
Ferraro, T.N.2
Dahl, J.P.3
Hildebrandt, M.A.4
Scattergood, T.M.5
O'Connor, M.J.6
Sperling, M.R.7
Dlugos, D.J.8
Berrettini, W.H.9
Buono, R.J.10
-
87
-
-
0037206647
-
A receptor gamma 2 subunit gene in Chinese patients with childhood absence epilepsy
-
DOI 10.1016/S0304-3940(02)00805-4, PII S0304394002008054
-
Lu, J., Chen, Y., Zhang, Y., Pan, H., Wu, H., Xu, K., Liu, X., Jiang, Y., Bao, X., Ding, K., et al. (2002). Mutation screen of the GABAA receptor 2 subunit gene in Chinese patients with childhood absence epilepsy. Neurosci. Lett. 332, 75-78. (Pubitemid 35217844)
-
(2002)
Neuroscience Letters
, vol.332
, Issue.2
, pp. 75-78
-
-
Lu, J.1
Chen, Y.2
Zhang, Y.3
Pan, H.4
Wu, H.5
Xu, K.6
Liu, X.7
Jiang, Y.8
Bao, X.9
Ding, K.10
Shen, Y.11
Wu, X.12
-
88
-
-
84896801748
-
Association of IL-1-889C/T polymorphism with the risk of pediatric epilepsy
-
Lu, H.-y., Huang, S.-m., Zhang, A.-h., Zheng, G., and Huang, Y.-j. (2009). Association of IL-1-889C/T polymorphism with the risk of pediatric epilepsy. Acta Univ. Med. Nanjing (Natural Science) 8, 023.
-
(2009)
Acta Univ. Med. Nanjing (Natural Science)
, vol.8
, pp. 023
-
-
Lu, H.-Y.1
Huang, S.-M.2
Zhang, A.-H.3
Zheng, G.4
Huang, Y.-J.5
-
89
-
-
3943081925
-
Five single nucleotide polymorphisms of casein kinase I gamma 2 gene in children with familial febrile convulsions
-
Ma, Y.N., Hao, L., Niu, S.L., Xu, Y.F., Zhang, Y., Pei, P., Bu, D.F., and Qi, Y. (2004). Five single nucleotide polymorphisms of casein kinase I 2 gene in children with familial febrile convulsions. Zhonghua yi xue yi chuan xue za zhi Zhonghua yixue yichuanxue zazhi Chin. J. Med. Genet. 21, 347-350. (Pubitemid 39050040)
-
(2004)
Chinese Journal of Medical Genetics
, vol.21
, Issue.4
, pp. 347-350
-
-
Ma, Y.-N.1
Hao, L.2
Niu, S.-L.3
Xu, Y.-F.4
Zhang, Y.5
Pei, P.6
Bu, D.-F.7
Qi, Y.8
-
90
-
-
26444567845
-
The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures
-
Ma, S., Abou-Khalil, B., Sutcliffe, J.S., Haines, J.L., and Hedera, P. (2005a). The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures. BMC Med. Genet. 6, 13.
-
(2005)
BMC Med. Genet.
, vol.6
, pp. 13
-
-
Ma, S.1
Abou-Khalil, B.2
Sutcliffe, J.S.3
Haines, J.L.4
Hedera, P.5
-
91
-
-
15844431547
-
Association between familial febrile convulsions and HCN2 gene
-
Ma, Y., Chen, Z., Zou, L., Zhang, Y., Niu, S., Xu, Y., Pei, P., Bu, D.F., and Qi, Y. (2005b). Association between familial febrile convulsions and HCN2 gene. Zhonghua yi xue za zhi 85, 663-666. (Pubitemid 40425407)
-
(2005)
National Medical Journal of China
, vol.85
, Issue.10
, pp. 663-666
-
-
Ma, Y.-N.1
Chen, Z.-Y.2
Zou, L.-P.3
Zhang, Y.4
Niu, S.-L.5
Xu, Y.-F.6
Pei, P.7
Bu, D.-F.8
Qi, Y.9
-
92
-
-
84856495418
-
High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern Newfoundland
-
Mahoney, K., Buckley, D., Alam, M., Penney, S., Young, T.-L., Parfrey, P., and Moore, S.J. (2012). High incidence of pediatric idiopathic epilepsy is associated with familial and autosomal dominant disease in Eastern Newfoundland. Epilepsy Res. 98, 140-147.
-
(2012)
Epilepsy Res.
, vol.98
, pp. 140-147
-
-
Mahoney, K.1
Buckley, D.2
Alam, M.3
Penney, S.4
Young, T.-L.5
Parfrey, P.6
Moore, S.J.7
-
93
-
-
77951662687
-
High-density SNP screen of sodium channel genes by haplotype tagging and DNA pooling for association with idiopathic generalized epilepsy
-
Makoff, A., Lai, T., Barratt, C., Valentin, A., Moran, N., Asherson, P., and Nashef, L. (2010). High-density SNP screen of sodium channel genes by haplotype tagging and DNA pooling for association with idiopathic generalized epilepsy. Epilepsia 51, 694-698.
-
(2010)
Epilepsia
, vol.51
, pp. 694-698
-
-
Makoff, A.1
Lai, T.2
Barratt, C.3
Valentin, A.4
Moran, N.5
Asherson, P.6
Nashef, L.7
-
94
-
-
29144515651
-
v1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures
-
DOI 10.1073/pnas.0506818102
-
Mantegazza, M., Gambardella, A., Rusconi, R., Schiavon, E., Annesi, F., Cassulini, R.R., Labate, A., Carrideo, S., Chifari, R., Canevini, M.P., et al. (2005). Identification of an Nav1.1 sodium channel (SCN1A) loss-of-function mutation associated with familial simple febrile seizures. Proc. Natl. Acad. Sci. USA 102, 18177-18182. (Pubitemid 41798521)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.50
, pp. 18177-18182
-
-
Mantegazza, M.1
Gambardella, A.2
Rusconi, R.3
Schiavon, E.4
Annesi, F.5
Cassulini, R.R.6
Labate, A.7
Carrideo, S.8
Chifari, R.9
Canevini, M.P.10
Canger, R.11
Franceschetti, S.12
Annesi, G.13
Wanke, E.14
Quattrone, A.15
-
95
-
-
33746200051
-
Increased IL-1β Production From dsRNA-stimulated Leukocytes in Febrile Seizures
-
DOI 10.1016/j.pediatrneurol.2005.12.005, PII S0887899406000464
-
Matsuo, M., Sasaki, K., Ichimaru, T., Nakazato, S., and Hamasaki, Y. (2006). Increased IL-1production from dsRNA-stimulated leukocytes in febrile seizures. Pediatr. Neurol. 35, 102-106. (Pubitemid 44093976)
-
(2006)
Pediatric Neurology
, vol.35
, Issue.2
, pp. 102-106
-
-
Matsuo, M.1
Sasaki, K.2
Ichimaru, T.3
Nakazato, S.4
Hamasaki, Y.5
-
96
-
-
0031882602
-
Univariate genetic analyses of epilepsy and seizures in a population- based twin study: The Virginia twin registry
-
DOI 10.1002/(SICI)1098-2272(1998)15:1<33::AID-GEPI3>3.0.CO;2-5
-
Miller, L.L., Pellock, J.M., DeLorenzo, R.J., Meyer, J.M., and Corey, L.A. (1998). Univariate genetic analyses of epilepsy and seizures in a population-based twin study: the Virginia Twin Registry. Genet. Epidemiol. 15, 33-49. (Pubitemid 28096208)
-
(1998)
Genetic Epidemiology
, vol.15
, Issue.1
, pp. 33-49
-
-
Miller, L.L.1
Pellock, J.M.2
DeLorenzo, R.J.3
Meyer, J.M.4
Corey, L.A.5
-
97
-
-
0032892015
-
Epilepsy and seizure occurrence in a population-based sample of Virginian twins and their families
-
DOI 10.1016/S0920-1211(98)00113-2, PII S0920121198001132
-
Miller, L.L., Pellock, J.M., Boggs, J.G., DeLorenzo, R.J., Meyer, J.M., and Corey, L.A. (1999). Epilepsy and seizure occurrence in a population-based sample of Virginian twins and their families. Epilepsy Res. 34, 135-143. (Pubitemid 29155484)
-
(1999)
Epilepsy Research
, vol.34
, Issue.2-3
, pp. 135-143
-
-
Miller, L.L.1
Pellock, J.M.2
Boggs, J.G.3
DeLorenzo, R.J.4
Meyer, J.M.5
Corey, L.A.6
-
98
-
-
33747877638
-
Role of Viral Infections in the Etiology of Febrile Seizures
-
DOI 10.1016/j.pediatrneurol.2006.06.004, PII S0887899406003791
-
Millichap, J.G. and Millichap, J.J. (2006). Role of viral infections in the etiology of febrile seizures. Pediatr. Neurol. 35, 165-172. (Pubitemid 44291533)
-
(2006)
Pediatric Neurology
, vol.35
, Issue.3
, pp. 165-172
-
-
Millichap, J.G.1
Millichap, J.J.2
-
99
-
-
0033361895
-
Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33
-
DOI 10.1086/302621
-
Moulard, B., Chaigne, D., Mouthon, D., Buresi, C., Guipponi, M., and Malafosse, A. (1999). Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33. Am. J. Hum. Genet. 65, 1396-1400. (Pubitemid 30460390)
-
(1999)
American Journal of Human Genetics
, vol.65
, Issue.5
, pp. 1396-1400
-
-
Moulard, B.1
Guipponi, M.2
Chaigne, D.3
Mouthon, D.4
Buresi, C.5
Malafosse, A.6
-
100
-
-
2342644850
-
Febrile convulsions and genetic susceptibility: Role of the neuronal nicotinic acetylcholine receptor 4 subunit
-
Mulley, J., Heron, S., Scheffer, I., and Berkovic, S. (2004). Febrile convulsions and genetic susceptibility: role of the neuronal nicotinic acetylcholine receptor 4 subunit. Epilepsia 45, 561.
-
(2004)
Epilepsia
, vol.45
, pp. 561
-
-
Mulley, J.1
Heron, S.2
Scheffer, I.3
Berkovic, S.4
-
101
-
-
0036894233
-
A locus for simple pure febrile seizures maps to chromosome 6q22-q24
-
Nabbout, R., Prud'homme, J.F., Herman, A., Feingold, J., Brice, A., Dulac, O., and LeGuern, E. (2002). A locus for simple pure febrile seizures maps to chromosome 6q22-q24. Brain 125, 2668-2680. (Pubitemid 35423516)
-
(2002)
Brain
, vol.125
, Issue.12
, pp. 2668-2680
-
-
Nabbout, R.1
Prud'Homme, J.-F.2
Herman, A.3
Feingold, J.4
Brice, A.5
Dulac, O.6
LeGuern, E.7
-
102
-
-
34247539428
-
New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p
-
DOI 10.1212/01.wnl.0000260062.02829.e3, PII 0000611420070424000010
-
Nabbout, R., Baulac, S., Desguerre, I., Bahi-Buisson, N., Chiron, C., Ruberg, M., Dulac, O., and LeGuern, E. (2007). New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p. Neurology 68, 1374-1381. (Pubitemid 46659089)
-
(2007)
Neurology
, vol.68
, Issue.17
, pp. 1374-1381
-
-
Nabbout, R.1
Baulac, S.2
Desguerre, I.3
Bahi-Buisson, N.4
Chiron, C.5
Ruberg, M.6
Dulac, O.7
LeGuern, E.8
-
103
-
-
17344375789
-
Significant evidence for linkage of febrile seizures to chromosome 5q14-q15
-
Nakayama, J., Hamano, K., Iwasaki, N., Nakahara, S., Horigome, Y., Saitoh, H., Aoki, T., Maki, T., Kikuchi, M., Migita, T., et al. (2000). Significant evidence for linkage of febrile seizures to chromosome 5q14-q15. Hum. Mol. Gen. 9, 87-91. (Pubitemid 30145292)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.1
, pp. 87-91
-
-
Nakayama, J.1
Hamano, K.2
Iwasaki, N.3
Nakahara, S.4
Horigome, Y.5
Saitoh, H.6
Aoki, T.7
Maki, T.8
Kikuchi, M.9
Migita, T.10
Ohto, T.11
Yokouchi, Y.12
Tanaka, R.13
Hasegawa, M.14
Matsui, A.15
Hamaguchi, H.16
Arinami, T.17
-
104
-
-
0037199677
-
Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans
-
DOI 10.1016/S0304-3940(02)00651-1, PII S0304394002006511
-
Nakayama, J., Yamamoto, N., Hamano, K., Iwasaki, N., Ohta, M., Nakahara, S., Horigome, Y., Nakahara, C., Noguchi, E., Shiono, J., et al. (2002). Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans. Neurosci. Lett. 329, 249-251. (Pubitemid 34880085)
-
(2002)
Neuroscience Letters
, vol.329
, Issue.2
, pp. 249-251
-
-
Nakayama, J.1
Yamamoto, N.2
Hamano, K.3
Iwasaki, N.4
Ohta, M.5
Nakahara, S.6
Horigome, Y.7
Nakahara, C.8
Noguchi, E.9
Shiono, J.10
Shimakura, Y.11
Yamakawa-Kobayashi, K.12
Matsui, A.13
Arinami, T.14
-
105
-
-
0242720549
-
Mutation Analysis of the Leucine-Rich, Glioma Inactivated 1 Gene (LGI1) in Japanese Febrile Seizure Patients
-
DOI 10.1055/s-2003-43255
-
Nakayama, J., Hamano, K., Iwasaki, N., Ohta, M., Nakahara, S., Matsui, A., and Arinami, T. (2003a). Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients. Neuropediatrics 34, 234-236. (Pubitemid 37411729)
-
(2003)
Neuropediatrics
, vol.34
, Issue.5
, pp. 234-236
-
-
Nakayama, J.1
Hamano, K.2
Iwasaki, N.3
Ohta, M.4
Nakahara, S.5
Matsui, A.6
Arinami, T.7
-
106
-
-
0038324191
-
A-receptor γ2 subunit (GABRG2) gene in Japanese febrile seizure patients
-
DOI 10.1016/S0304-3940(03)00338-0
-
Nakayama, J., Hamano, K., Noguchi, E., Horiuchi, Y., Iwasaki, N., Ohta, M., Nakahara, S., Naoi, T., Matsui, A., Arinami, T. (2003b). Failure to find causal mutations in the GABAA-receptor 2 subunit (GABRG2) gene in Japanese febrile seizure patients. Neurosci. Lett. 343, 117-120. (Pubitemid 36577529)
-
(2003)
Neuroscience Letters
, vol.343
, Issue.2
, pp. 117-120
-
-
Nakayama, J.1
Hamano, K.2
Noguchi, E.3
Horiuchi, Y.4
Iwasaki, N.5
Ohta, M.6
Nakahara, S.7
Naoi, T.8
Matsui, A.9
Arinami, T.10
-
107
-
-
8844220357
-
Linkage and association of febrile seizures to the IMPA2 gene on human chromosome 18
-
Nakayama, J., Yamamoto, N., Hamano, K., Iwasaki, N., Ohta, M., Nakahara, S., Matsui, A., Noguchi, E., and Arinami, T. (2004). Linkage and association of febrile seizures to the IMPA2 gene on human chromosome 18. Neurology 63, 1803-1807. (Pubitemid 39532372)
-
(2004)
Neurology
, vol.63
, Issue.10
, pp. 1803-1807
-
-
Nakayama, J.1
Yamamoto, N.2
Hamano, K.3
Iwasaki, N.4
Ohta, M.5
Nakahara, S.6
Matsui, A.7
Noguchi, E.8
Arinami, T.9
-
108
-
-
84860745721
-
Long-term risk of developing epilepsy after febrile seizures: A prospective cohort study
-
Neligan, A., Bell, G.S., Giavasi, C., Johnson, A.L., Goodridge, D.M., Shorvon, S.D., and Sander, J.W. (2012). Long-term risk of developing epilepsy after febrile seizures: a prospective cohort study. Neurology 78, 1166-1170.
-
(2012)
Neurology
, vol.78
, pp. 1166-1170
-
-
Neligan, A.1
Bell, G.S.2
Giavasi, C.3
Johnson, A.L.4
Goodridge, D.M.5
Shorvon, S.D.6
Sander, J.W.7
-
109
-
-
0017813302
-
Prognosis in children with febrile seizures
-
Nelson, K.B. and Ellenberg, J.H. (1978). Prognosis in children with febrile seizures. Pediatrics 61, 720-727. (Pubitemid 8314594)
-
(1978)
Pediatrics
, vol.61
, Issue.5
, pp. 720-727
-
-
Nelson, K.B.1
Ellenberg, J.H.2
-
110
-
-
0034455833
-
Circulating cytokines as mediators of fever
-
DOI 10.1086/317513
-
Netea, M.G., Kullberg, B.J., and Van der Meer, J.W.M. (2000). Circulating cytokines as mediators of fever. Clin. Infect. Dis. 31, S178-S184. (Pubitemid 32291108)
-
(2000)
Clinical Infectious Diseases
, vol.31
, Issue.SUPPL. 5
-
-
Netea, M.G.1
Kullberg, B.J.2
Van Der Meer, J.W.M.3
-
111
-
-
48449092930
-
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
-
Neubauer, B.A., Waldegger, S., Heinzinger, J., Hahn, A., Kurlemann, G., Fiedler, B., Eberhard, F., Muhle, H., Stephani, U., Garkisch, S., et al. (2008). KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes. Neurology 71, 177-183.
-
(2008)
Neurology
, vol.71
, pp. 177-183
-
-
Neubauer, B.A.1
Waldegger, S.2
Heinzinger, J.3
Hahn, A.4
Kurlemann, G.5
Fiedler, B.6
Eberhard, F.7
Muhle, H.8
Stephani, U.9
Garkisch, S.10
-
112
-
-
84555190633
-
Interleukin-6 gene polymorphism in febrile seizures
-
Nur, B.G., Kahramaner, Z., Duman, O., Dundar, N.O., Sallakc, N., Yavuzer, U., and Haspolat, S. (2012). Interleukin-6 gene polymorphism in febrile seizures. Pediatr. Neurol. 46, 36-38.
-
(2012)
Pediatr. Neurol.
, vol.46
, pp. 36-38
-
-
Nur, B.G.1
Kahramaner, Z.2
Duman, O.3
Dundar, N.O.4
Sallakc, N.5
Yavuzer, U.6
Haspolat, S.7
-
113
-
-
84865049224
-
Single nucleotide polymorphism and production of IL-1and IL-10 cytokines in febrile seizures
-
Nur, B.G., Sahinturk, D., Coskun, M., Duman, O., Yavuzer, U., and Haspolat, S. (2012). Single nucleotide polymorphism and production of IL-1and IL-10 cytokines in febrile seizures. Neuropediatrics 43, 194-200.
-
(2012)
Neuropediatrics
, vol.43
, pp. 194-200
-
-
Nur, B.G.1
Sahinturk, D.2
Coskun, M.3
Duman, O.4
Yavuzer, U.5
Haspolat, S.6
-
114
-
-
0026542798
-
Seizure recurrence after a first febrile seizure: A multivariate approach
-
Offringa, M., Derksen-Lubsen, G., Bossuyt, P.M., and Lubsen, J. (1992). Seizure recurrence after a first febrile seizure: a multivariate approach. Dev. Med. Child Neurol. 34, 15-24.
-
(1992)
Dev. Med. Child Neurol.
, vol.34
, pp. 15-24
-
-
Offringa, M.1
Derksen-Lubsen, G.2
Bossuyt, P.M.3
Lubsen, J.4
-
115
-
-
0028353932
-
Risk factors for seizure recurrence in children with febrile seizures: A pooled analysis of individual patient data from five studies
-
Offringa, M., Bossuyt, P.M.M., Lubsen, J., Ellenberg, J.H., Nelson, K.B., Knudsen, F.U., Annegers, J.F., el-Radhi, A.S., Habbema, J.D., Derksen-Lubsen, G., et al. (1994). Risk factors for seizure recurrence in children with febrile seizures: a pooled analysis of individual patient data from five studies. J. Pediatr. 124, 574-584. (Pubitemid 24128153)
-
(1994)
Journal of Pediatrics
, vol.124
, Issue.4
, pp. 574-584
-
-
Offringa, M.1
Bossuyt, P.M.M.2
Lubsen, J.3
Ellenberg, J.H.4
Nelson, K.B.5
Knudsen, F.U.6
Annegers, J.F.7
El-Radhi, A.S.M.8
Habbema, J.D.F.9
Derksen-Lubsen, G.10
Hauser, W.A.11
Kurland, L.T.12
Banajeh, S.M.A.13
Larsen, S.14
-
116
-
-
33744509305
-
Lack of association between IL-1β/α gene polymorphisms and temporal lobe epilepsy with hippocampal sclerosis
-
DOI 10.1016/j.seizure.2006.02.016, PII S1059131106000422
-
Ozkara, C., Uzan, M., Tanriverdi, T., Baykara, O., Ekinci, B., Yeni, N., Kafadar, A., and Buyru, N. (2006). Lack of association between IL-1/gene polymorphisms and temporal lobe epilepsy with hippocampal sclerosis. Seizure 15, 288-291. (Pubitemid 43812239)
-
(2006)
Seizure
, vol.15
, Issue.5
, pp. 288-291
-
-
Ozkara, C.1
Uzan, M.2
Tanriverdi, T.3
Baykara, O.4
Ekinci, B.5
Yeni, N.6
Kafadar, A.7
Buyru, N.8
-
117
-
-
0032834017
-
A locus for febrile seizures (FEB3) maps to chromosome 2q23-24
-
DOI 10.1002/1531-8249(199910)46:4<671::AID-ANA20>3.0.CO;2-5
-
Peiffer, A., Thompson, J., Charlier, C., Otterud, B., Varvil, T., Pappas, C., Barnitz, C., Gruenthal, K., Kuhn, R., and Leppert, M. (1999). A locus for febrile seizures (FEB3) maps to chromosome 2q23-24. Ann. Neurol. 46, 671-678. (Pubitemid 29466451)
-
(1999)
Annals of Neurology
, vol.46
, Issue.4
, pp. 671-678
-
-
Peiffer, A.1
Thompson, J.2
Charlier, C.3
Otterud, B.4
Varvil, T.5
Pappas, C.6
Barnitz, C.7
Gruenthal, K.8
Kuhn, R.9
Leppert, M.10
-
118
-
-
0034899318
-
Polymorphism of the interleukin-1 gene complex in localization-related epilepsy [4]
-
Peltola, J., Keränen, T., Rainesalo, S., and Hurme, M. (2001). Polymorphism of the interleukin-1 gene complex in localization-related epilepsy. Ann. Neurol. 50, 275-276. (Pubitemid 32738160)
-
(2001)
Annals of Neurology
, vol.50
, Issue.2
, pp. 275-276
-
-
Peltola, J.1
Keranen, T.2
Rainesalo, S.3
Hurme, M.4
-
119
-
-
1642346251
-
Association of the nicotinic receptor beta 2 subunit and febrile seizures
-
DOI 10.1016/j.pediatrneurol.2003.08.001, PII S0887899403004363
-
Peng, C.-T., Chou, I.C., Li, C.-I., Hsu, Y.-A., Tsai, C.-H., and Tsai, F.-J. (2004). Association of the nicotinic receptor 2 subunit and febrile seizures. Pediatr. Neurol. 30, 186-189. (Pubitemid 38366444)
-
(2004)
Pediatric Neurology
, vol.30
, Issue.3
, pp. 186-189
-
-
Peng, C.-T.1
Chou, I.-C.2
Li, C.-I.3
Hsu, Y.-A.4
Tsai, C.-H.5
Tsai, F.-J.6
-
120
-
-
73349143949
-
Lack of replication of association between SCN1A SNP and febrile seizures
-
Petrovski, S., Scheffer, I.E., Sisodiya, S.M., O'Brien, T.J., Berkovic, S.F., Consortium ObotE. (2009). Lack of replication of association between SCN1A SNP and febrile seizures. Neurology 73, 1928-1930.
-
(2009)
Neurology
, vol.73
, pp. 1928-1930
-
-
Petrovski, S.1
Scheffer, I.E.2
Sisodiya, S.M.3
O'Brien, T.J.4
Berkovic, S.F.5
Consortium, O.E.6
-
121
-
-
84855960242
-
From virus to inflammation: Mechanisms of RIG-I-induced IL-1production
-
Poeck, H. and Ruland, J. (2012). From virus to inflammation: mechanisms of RIG-I-induced IL-1production. Eur. J. Cell Biol. 91, 59-64.
-
(2012)
Eur. J. Cell Biol.
, vol.91
, pp. 59-64
-
-
Poeck, H.1
Ruland, J.2
-
122
-
-
84859250966
-
Role of MDR1 C3435T and GABRG2 C588T gene polymorphisms in seizure occurrence and MDR1 effect on anti-epileptic drug (phenytoin) absorption
-
Ponnala, S., Chaudhari, J.R., Jaleel, M.A., Bhiladvala, D., Kaipa, P.R., Das, U.N., and Hasan, Q. (2012). Role of MDR1 C3435T and GABRG2 C588T gene polymorphisms in seizure occurrence and MDR1 effect on anti-epileptic drug (phenytoin) absorption. Genet. Test. Mol. Biomark. 16, 550-557.
-
(2012)
Genet. Test. Mol. Biomark.
, vol.16
, pp. 550-557
-
-
Ponnala, S.1
Chaudhari, J.R.2
Jaleel, M.A.3
Bhiladvala, D.4
Kaipa, P.R.5
Das, U.N.6
Hasan, Q.7
-
123
-
-
69549097625
-
The 1674+11C T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy
-
Rozycka, A., Steinborn, B., and Trzeciak, W.H. (2009). The 1674+11C T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy. Seizure 18, 601-603.
-
(2009)
Seizure
, vol.18
, pp. 601-603
-
-
Rozycka, A.1
Steinborn, B.2
Trzeciak, W.H.3
-
124
-
-
0344117156
-
Autosomal dominant nocturnal frontal lobe epilepsy in a Spanish family with a Ser252Phe mutation in the CHRNA4 gene
-
DOI 10.1001/archneur.56.8.1004
-
Sáenz, A, Galán, J., Caloustian, C., Lorenzo, F., Márquez, C., Rodríguez, N., Jiménez, M.D., Poza, J.J., Cobo, A.M., Grid, D., et al. (1999). Autosomal dominant nocturnal frontal lobe epilepsy in a Spanish family with a Ser252Phe mutation in the Chrna4 gene. Arch. Neurol. 56, 1004-1009. (Pubitemid 29374819)
-
(1999)
Archives of Neurology
, vol.56
, Issue.8
, pp. 1004-1009
-
-
Saenz, A.1
Galan, J.2
Caloustian, C.3
Lorenzo, F.4
Marquez, C.5
Rodriguez, N.6
Jimenez, M.D.7
Poza, J.J.8
Cobo, A.M.9
Grid, D.10
Prud'homme, J.F.11
De Munain, A.L.12
-
125
-
-
84871272736
-
GABRG2 gene polymorphisms in Egyptian children with simple febrile seizures
-
Salam, S., Rahman, H., and Karam, R. (2012). GABRG2 gene polymorphisms in Egyptian children with simple febrile seizures. Indian J. Pediatr. 79, 1-3.
-
(2012)
Indian J. Pediatr.
, vol.79
, pp. 1-3
-
-
Salam, S.1
Rahman, H.2
Karam, R.3
-
126
-
-
84856460055
-
Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy
-
Salzmann, A., Guipponi, M., Lyons, P.J., Fricker, L.D., Sapio, M., Lambercy, C., Buresi, C., Ouled Amar Bencheikh, B., Lahjouji, F., Ouazzani, R., et al. (2012). Carboxypeptidase A6 gene (CPA6) mutations in a recessive familial form of febrile seizures and temporal lobe epilepsy and in sporadic temporal lobe epilepsy. Hum. Mutat. 33, 124-135.
-
(2012)
Hum. Mutat.
, vol.33
, pp. 124-135
-
-
Salzmann, A.1
Guipponi, M.2
Lyons, P.J.3
Fricker, L.D.4
Sapio, M.5
Lambercy, C.6
Buresi, C.7
Ouled Amar Bencheikh, B.8
Lahjouji, F.9
Ouazzani, R.10
-
127
-
-
67649995458
-
BDNF gene polymorphism in patients with temporal lobe epilepsy
-
Sargin, G., Gürses, C., Naci, Ç., Bebek, N., Baykan, B., Özbek, U., and Ayen, G. (2008). BDNF gene polymorphism in patients with temporal lobe epilepsy. J. Neurol. Sci. (Turkish) 25, 220-225.
-
(2008)
J. Neurol. Sci. (Turkish)
, vol.25
, pp. 220-225
-
-
Sargin, G.1
Gürses, C.2
Naci, Ç.3
Bebek, N.4
Baykan, B.5
Özbek, U.6
Ayen, G.7
-
128
-
-
0030943313
-
Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes
-
DOI 10.1093/brain/120.3.479
-
Scheffer, I.E. and Berkovic, S.F. (1997). Generalized epilepsy with febrile seizures plus: a genetic disorder with heterogeneous clinical phenotypes. Brain 120, 479-490. (Pubitemid 27153640)
-
(1997)
Brain
, vol.120
, Issue.3
, pp. 479-490
-
-
Scheffer, I.E.1
Berkovic, S.F.2
-
129
-
-
64449088896
-
Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus
-
Scheffer, I.E., Zhang, Y.-H., Jansen, F.E., and Dibbens, L. (2009). Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus Brain Dev. 31, 394-400.
-
(2009)
Brain Dev.
, vol.31
, pp. 394-400
-
-
Scheffer, I.E.1
Zhang, Y.-H.2
Jansen, F.E.3
Dibbens, L.4
-
130
-
-
64049095461
-
A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures
-
Schlachter, K., Gruber-Sedlmayr, U., Stogmann, E., Lausecker, M., Hotzy, C., Balzar, J., Schuh, E., Baumgartner, C., Mueller, J.C., Illig, T., et al. (2009). A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures. Neurology 72, 974-978.
-
(2009)
Neurology
, vol.72
, pp. 974-978
-
-
Schlachter, K.1
Gruber-Sedlmayr, U.2
Stogmann, E.3
Lausecker, M.4
Hotzy, C.5
Balzar, J.6
Schuh, E.7
Baumgartner, C.8
Mueller, J.C.9
Illig, T.10
-
131
-
-
58149169138
-
Febrile seizures: Interleukin 1and interleukin-1 receptor antagonist polymorphisms
-
Serdarolu, G., Alpman, A., Tosun, A., Pehlvan, S., Özknay, F., Tekgül, H., and Gökben, S. (2009). Febrile seizures: interleukin 1and interleukin-1 receptor antagonist polymorphisms. Pediatr. Neurol. 40, 113-116.
-
(2009)
Pediatr. Neurol.
, vol.40
, pp. 113-116
-
-
Serdarolu, G.1
-
132
-
-
84867582248
-
Febrile seizures: An epidemiological and outcome study of 482 cases
-
Sfaihi, L., Maaloul, I., Kmiha, S., Aloulou, H., Chabchoub, I., Kamoun, T., and Hachicha, M. (2012). Febrile seizures: an epidemiological and outcome study of 482 cases. Childs Nerv. Syst. 28, 1779-1784.
-
(2012)
Childs Nerv. Syst.
, vol.28
, pp. 1779-1784
-
-
Sfaihi, L.1
Maaloul, I.2
Kmiha, S.3
Aloulou, H.4
Chabchoub, I.5
Kamoun, T.6
Hachicha, M.7
-
133
-
-
70349668995
-
A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome
-
Singh, N.A., Pappas, C., Dahle, E.J., Claes, L.R.F., Pruess, T.H., De Jonghe, P., Thompson, J., Dixon, M., Gurnett, C., Peiffer, A., et al. (2009). A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome. PLoS Genet. 5, e1000649.
-
(2009)
PLoS Genet.
, vol.5
-
-
Singh, N.A.1
Pappas, C.2
Dahle, E.J.3
Claes, L.R.F.4
Pruess, T.H.5
De Jonghe, P.6
Thompson, J.7
Dixon, M.8
Gurnett, C.9
Peiffer, A.10
-
134
-
-
0030749655
-
Brief research communication: Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit α4 with common idiopathic generalized epilepsies
-
DOI 10.1002/(SICI)1096-8628(19970725)74:4<445::AID-AJMG18>3.0.CO;2- I
-
Steinlein, O., Sander, T., Stoodt, J., Kretz, R., Janz, D., and Propping, P. (1997). Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit 4 with common idiopathic generalized epilepsies. Am. J. Med. Genet. 74, 445-449. (Pubitemid 27349384)
-
(1997)
American Journal of Medical Genetics - Neuropsychiatric Genetics
, vol.74
, Issue.4
, pp. 445-449
-
-
Steinlein, O.1
-
135
-
-
0033606072
-
The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy
-
Steinlein, O.K., Stoodt, J., Biervert, C., Janz, D., and Sander, T. (1999). The voltage gated potassium channel KCNQ2 and idiopathic generalized epilepsy. NeuroReport 10, 1163-1166. (Pubitemid 29403687)
-
(1999)
NeuroReport
, vol.10
, Issue.6
, pp. 1163-1166
-
-
Steinlein, O.K.1
Stoodt, J.2
Biervert, C.3
Janz, D.4
Sander, T.5
-
136
-
-
84896786085
-
The association study of calcyphosine (CAPS) gene with familiar febrile convulsions
-
Sun, Y.-x., Xu, Z., and Ma, W.-n. (2005). The association study of calcyphosine (CAPS) gene with familiar febrile convulsions. Chin. J. Birth Health Hered. 7, 007.
-
(2005)
Chin. J. Birth Health Hered.
, vol.7
, pp. 007
-
-
Sun, Y.-X.1
Xu, Z.2
Ma, W.-N.3
-
137
-
-
84870296042
-
De-novo mutations and genetic variation in the SCN1A gene in Malaysian patients with generalized epilepsy with febrile seizures plus (GEFS+)
-
Tan, E.H., Razak, S.A., Abdullah, J.M., and Mohamed Yusoff, A.A. (2012). De-novo mutations and genetic variation in the SCN1A gene in Malaysian patients with generalized epilepsy with febrile seizures plus (GEFS+). Epilepsy Res. 102, 210-215.
-
(2012)
Epilepsy Res.
, vol.102
, pp. 210-215
-
-
Tan, E.H.1
Razak, S.A.2
Abdullah, J.M.3
Mohamed, Y.A.A.4
-
138
-
-
36549022629
-
Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy
-
DOI 10.1016/j.nbd.2007.08.006, PII S0969996107001854
-
Tang, B., Sander, T., Craven, K.B., Hempelmann, A., and Escayg, A. (2008). Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy. Neurobiol. Dis. 29, 59-70. (Pubitemid 350180483)
-
(2008)
Neurobiology of Disease
, vol.29
, Issue.1
, pp. 59-70
-
-
Tang, B.1
Sander, T.2
Craven, K.B.3
Hempelmann, A.4
Escayg, A.5
-
139
-
-
0037032589
-
Association analysis between the human interleukin 1β (-511) gene polymorphism and susceptibility to febrile convulsions
-
DOI 10.1016/S0304-3940(02)01069-8, PII S0304394002010698
-
Tilgen, N., Pfeiffer, H., Cobilanschi, J., Rau, B., Horvath, S., Elger, C.E., Propping, P., and Heils A. (2002). Association analysis between the human interleukin 1(-511) gene polymorphism and susceptibility to febrile convulsions. Neurosci. Lett. 334, 68-70. (Pubitemid 35335934)
-
(2002)
Neuroscience Letters
, vol.334
, Issue.1
, pp. 68-70
-
-
Tilgen, N.1
Pfeiffer, H.2
Cobilanschi, J.3
Rau, B.4
Horvath, S.5
Elger, C.E.6
Propping, P.7
Heils, A.8
-
140
-
-
84866165845
-
Do gene polymorphism in IL-1, TNF-and IL-6 influence therapeutic response in patients with drug refractory epilepsy
-
Tiwari, P., Dwivedi, R., Mansoori, N., Alam, R., Chauhan, U.K., Tripathi, M., and Mukhopadhyay, A.K. (2012). Do gene polymorphism in IL-1, TNF-and IL-6 influence therapeutic response in patients with drug refractory epilepsy Epilepsy Res. 101, 261-267.
-
(2012)
Epilepsy Res.
, vol.101
, pp. 261-267
-
-
Tiwari, P.1
Dwivedi, R.2
Mansoori, N.3
Alam, R.4
Chauhan, U.K.5
Tripathi, M.6
Mukhopadhyay, A.K.7
-
141
-
-
0036809772
-
Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures
-
DOI 10.1016/S0887-8994(02)00434-4, PII S0887899402004344
-
Tsai, F.-J., Chou, I.C., Hsieh, Y.-Y., Lee, C.-C., Lin, C.-C., and Tsai, C.-H. (2002a). Interleukin-4 intron 3 polymorphism is not related to susceptibility to febrile seizures. Pediatr. Neurol. 27, 271-274. (Pubitemid 35341698)
-
(2002)
Pediatric Neurology
, vol.27
, Issue.4
, pp. 271-274
-
-
Tsai, F.-J.1
Chou, I.-C.2
Hsieh, Y.-Y.3
Lee, C.-C.4
Lin, C.-C.5
Tsai, C.-H.6
-
142
-
-
0036263088
-
Polymorphisms for interleukin 1β exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions
-
Tsai, F., Hsieh, Y.-Y., Chang, C.-C., Lin, C.-C., and Tsai, C.H. (2002b). Polymorphisms for interleukin 1exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions. Arch. Pediatr. Adolesc. Med. 156, 545-548. (Pubitemid 34596182)
-
(2002)
Archives of Pediatrics and Adolescent Medicine
, vol.156
, Issue.6
, pp. 545-548
-
-
Tsai, F.-J.1
Hsieh, Y.-Y.2
Chang, C.-C.3
Lin, C.-C.4
Tsai, C.-H.5
-
143
-
-
0023142341
-
Genetic analysis of febrile convulsions: Twin and family studies
-
Tsuboi, T. (1987). Genetic analysis of febrile convulsions: twin and family studies. Hum. Genet. 75, 7-14. (Pubitemid 17013668)
-
(1987)
Human Genetics
, vol.75
, Issue.1
, pp. 7-14
-
-
Tsuboi, T.1
-
144
-
-
0034946105
-
Proinflammatory cytokines, prostaglandins and zinc in febrile convulsions
-
Tütüncüolu, S., Kütükçüler, N., Kepe, L., Çoker, C., Berdeli, A., and Tekgül, H. (2001). Proinflammatory cytokines, prostaglandins and zinc in febrile convulsions. Pediatr. Int. 43, 235-239.
-
(2001)
Pediatr. Int.
, vol.43
, pp. 235-239
-
-
Tütüncüolu, S.1
-
145
-
-
84862308391
-
Lack of association of childhood partial epilepsy with brain derived neurotrophic factor gene
-
Unalp, A., Bora, E., Cankaya, T., Giray Bozkaya, O., Ercal, D., Ozturk, A., and Ulgenalp, A. (2012). Lack of association of childhood partial epilepsy with brain derived neurotrophic factor gene. ScientificWorldJournal 2012, 414797.
-
(2012)
ScientificWorldJournal
, vol.2012
, pp. 414797
-
-
Unalp, A.1
Bora, E.2
Cankaya, T.3
Giray Bozkaya, O.4
Ercal, D.5
Ozturk, A.6
Ulgenalp, A.7
-
146
-
-
0031956494
-
Prediction of febrile seizures in siblings: A practical approach
-
DOI 10.1007/s004310050824
-
van Esch, A., Steyerberg, E.W., van Duijn, C.M., Offringa, M., Derksen-Lubsen, G., van Steensel-Moll, H.A. (1998). Prediction of febrile seizures in siblings: a practical approach. Eur. J. Pediatr. 157, 340-344. (Pubitemid 28178140)
-
(1998)
European Journal of Pediatrics
, vol.157
, Issue.4
, pp. 340-344
-
-
Van Esch, A.1
Steyerberg, E.W.2
Van Duijn, C.M.3
Offringa, M.4
Derksen-Lubsen, G.5
Van Steensel-Moll, H.A.6
-
147
-
-
0036214453
-
Increased frequency of interleukin-1β (-511) allele 2 in febrile seizures
-
DOI 10.1016/S0887-8994(01)00380-0, PII S0887899401003800
-
Virta, M., Hurme, M., and Helminen, M. (2002a). Increased frequency of interleukin-1(-511) allele 2 in febrile seizures. Pediatr. Neurol. 26, 192-195. (Pubitemid 34296531)
-
(2002)
Pediatric Neurology
, vol.26
, Issue.3
, pp. 192-195
-
-
Virta, M.1
Hurme, M.2
Helminen, M.3
-
148
-
-
0036340601
-
Increased plasma levels of pro- and anti-inflammatory cytokines in patients with febrile seizures
-
DOI 10.1046/j.1528-1157.2002.02002.x
-
Virta, M., Hurme, M., and Helminen, M. (2002b). Increased plasma levels of pro-and anti-inflammatory cytokines in patients with febrile seizures. Epilepsia 43, 920-923. (Pubitemid 34857869)
-
(2002)
Epilepsia
, vol.43
, Issue.8
, pp. 920-923
-
-
Virta, M.1
Hurme, M.2
Helminen, M.3
-
149
-
-
0141535180
-
Interleukin-1β enhances NMDA receptor-mediated intracellular calcium increase through activation of the Src family of kinases
-
Viviani, B., Bartesaghi, S., Gardoni, F., Vezzani, A., Behrens, M.M., Bartfai, T., Binaglia, M., Corsini, E., Di Luca, M., Galli, C.L., et al. (2003). Interleukin-1enhances NMDA receptor-mediated intracellular calcium increase through activation of the Src family of kinases. J. Neurosci. 23, 8692-8700. (Pubitemid 37176649)
-
(2003)
Journal of Neuroscience
, vol.23
, Issue.25
, pp. 8692-8700
-
-
Viviani, B.1
Bartesaghi, S.2
Gardoni, F.3
Vezzani, A.4
Behrens, M.M.5
Bartfai, T.6
Binaglia, M.7
Corsini, E.8
Di Luca, M.9
Galli, C.L.10
Marinovich, M.11
-
150
-
-
34547907439
-
Lack of evidence for association between D2S124 and D2S111 polymorphisms of the SCN2A gene and idiopathic generalized epilepsy with generalized tonic-clonic seizures
-
DOI 10.1177/0883073807304706
-
Volzone, A., Rizzo, R., Gagliano, A., Palmarino, M., Lucarelli, P., Arpino, C., and Curatolo, P. (2007). Lack of evidence for association between D2S124 and D2S111 polymorphisms of the SCN2A gene and idiopathic generalized epilepsy with generalized tonic-clonic seizures. J. Child Neurol. 22, 907-910. (Pubitemid 47261249)
-
(2007)
Journal of Child Neurology
, vol.22
, Issue.7
, pp. 907-910
-
-
Volzone, A.1
Rizzo, R.2
Gagliano, A.3
Palmarino, M.4
Lucarelli, P.5
Arpino, C.6
Curatolo, P.7
-
151
-
-
0029881889
-
Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21
-
Wallace, R.H., Berkovic, S.F., Howell, R.A., Sutherland, G.R., and Mulley, J.C. (1996). Suggestion of a major gene for familial febrile convulsions mapping to 8q13-21. J. Med. Genet. 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
-
152
-
-
0035033520
-
A receptor γ2-subunit in childhood absence epilepsy and febrile seizures
-
DOI 10.1038/88259
-
Wallace, R.H., Marini, C., Petrou, S., Harkin, L.A., Bowser, D.N., Panchal, R.G., Williams, D.A., Sutherland, G.R., Mulley, J.C., Scheffer, I.E., et al. (2001). Mutant GABAA receptor 2-subunit in childhood absence epilepsy and febrile seizures. Nature Genet. 28, 49-52. (Pubitemid 32405816)
-
(2001)
Nature Genetics
, vol.28
, Issue.1
, pp. 49-52
-
-
Wallace, R.H.1
Marini, C.2
Petrou, S.3
Harkin, L.A.4
Bowser, D.N.5
Panchal, R.G.6
Williams, D.A.7
Sutherland, G.R.8
Mulley, J.C.9
Scheffer, I.E.10
Berkovic, S.F.11
-
153
-
-
0033621660
-
Interleukin-1β inhibits γ-aminobutyric acid type A (GABA(A)) receptor current in cultured hippocampal neurons
-
Wang, S., Cheng, Q., Malik, S., and Yang, J. (2000). Interleukin-1 inhibits -aminobutyric acid type A (GABAA) receptor current in cultured hippocampal neurons. J. Pharmacol. Exp. Ther. 292, 497-504. (Pubitemid 30067411)
-
(2000)
Journal of Pharmacology and Experimental Therapeutics
, vol.292
, Issue.2
, pp. 497-504
-
-
Wang, S.1
Cheng, Q.2
Malik, S.3
Yang, J.4
-
154
-
-
34447124334
-
Association analysis of 2 subunit of -aminobutyric acid (GABA) type A receptor and voltage-gated sodium channel type II -polypeptide gene mutation in Southern Chinese children with febrile seizures
-
Wang, X., Xu, M., and Du, L. (2007). Association analysis of 2 subunit of -aminobutyric acid (GABA) type A receptor and voltage-gated sodium channel type II -polypeptide gene mutation in Southern Chinese children with febrile seizures. J. Child Neurol. 22, 714-719.
-
(2007)
J. Child Neurol.
, vol.22
, pp. 714-719
-
-
Wang, X.1
Xu, M.2
Du, L.3
-
155
-
-
3242878101
-
Febrile seizures: An update
-
Waruiru, C. and Appleton, R. (2004). Febrile seizures: an update. Arch. Dis. Child. 89, 751-756.
-
(2004)
Arch. Dis. Child.
, vol.89
, pp. 751-756
-
-
Waruiru, C.1
Appleton, R.2
-
156
-
-
84896742659
-
Single nucleotide polymorphisms of GABRG2 in idiopathic generalized epilepsies (IGEs
-
Yeon, Y.H., Seung, S.J., Hwang, H.S., Kim, E., Kim, Y.H., Lee, I.G., et al. (2007). Single nucleotide polymorphisms of GABRG2 in idiopathic generalized epilepsies (IGEs). J. Korean Child Neurol. Soc. 15, 148-153.
-
(2007)
J. Korean Child Neurol. Soc.
, vol.15
, pp. 148-153
-
-
Yeon, Y.H.1
Seung, S.J.2
Hwang, H.S.3
Kim, E.4
Kim, Y.H.5
Lee, I.G.6
-
157
-
-
4444361243
-
Polymorphisms of casein kinase I gamma 2 gene associated with simple febrile seizures in Chinese Han population
-
DOI 10.1016/j.neulet.2004.06.054, PII S0304394004007840
-
Yinan, M., Yu, Q., Zhiyue, C., Jianjun, L., Lie, H., Liping, Z., Jianhui, Z., Fang, S., Dingfang, B., Qing, L., et al. (2004). Polymorphisms of casein kinase I 2 gene associated with simple febrile seizures in Chinese Han population. Neurosci. Lett. 368, 2-6. (Pubitemid 39178736)
-
(2004)
Neuroscience Letters
, vol.368
, Issue.1
, pp. 2-6
-
-
Yinan, M.1
Yu, Q.2
Zhiyue, C.3
Jianjun, L.4
Lie, H.5
Liping, Z.6
Jianhui, Z.7
Fang, S.8
Dingfang, B.9
Qing, L.10
Xiru, W.11
-
158
-
-
33845546998
-
HCN2, NRTN, CAPS and GPX4 genes are not associated with simple febrile seizures in Chinese Han population
-
Yinan, M.A., Yu, Q., Zhiyue, C., Liping, Z., Fang, F., Liwen, W., Fuying, S., Jianhui, Z., Dingfang, B., Tianjun, W., et al. (2006). HCN2, NRTN, CAPS and GPX4 genes are not associated with simple febrile seizures in Chinese Han population. J. Pediatr. Neurol. 4, 83-87. (Pubitemid 44920958)
-
(2006)
Journal of Pediatric Neurology
, vol.4
, Issue.2
, pp. 83-87
-
-
Yinan, M.A.1
Yu, Ql.2
Zhiyue, C.3
Liping, Z.4
Fang, F.5
Liwen, W.6
Fuying, S.7
Jianhui, Z.8
Dingfang, B.9
Tianjun, W.10
Qing, L.11
Xiru, W.12
-
159
-
-
84896748602
-
Polymorphisms of interleukin-1promoter in simple febrile seizures
-
Yoon, J.W., Choen, E.J., and Lee, Y.H. (2008). Polymorphisms of interleukin-1promoter in simple febrile seizures. Korean J. Pediatr. 51, 1007-1011.
-
(2008)
Korean J. Pediatr.
, vol.51
, pp. 1007-1011
-
-
Yoon, J.W.1
Choen, E.J.2
Lee, Y.H.3
-
160
-
-
84859557060
-
Lack of association of SCN2A and KCNJ10 polymorphisms in Korean children with epilepsy: Intractability and relapse of epilepsy
-
Yoon, J., Choi, B., Park, Y., Kang, Y., Nam, S., Lee, J., and Park, W.S. (2012). Lack of association of SCN2A and KCNJ10 polymorphisms in Korean children with epilepsy: intractability and relapse of epilepsy. Mol. Cell. Toxicol. 8, 61-67.
-
(2012)
Mol. Cell. Toxicol.
, vol.8
, pp. 61-67
-
-
Yoon, J.1
Choi, B.2
Park, Y.3
Kang, Y.4
Nam, S.5
Lee, J.6
Park, W.S.7
-
161
-
-
84896778872
-
Association study on simple febrile seizures and casein kinase 1, gamma 1 gene [J]
-
Yu-jie1a, L., Yin-nan1b, M., Zu-geng, C., Gu1a, T., Li-ping, Z., Fang, F., et al. (2008). Association study on simple febrile seizures and casein kinase 1, gamma 1 gene [J]. J. Appl. Clin. Pediatr. 4, 025.
-
(2008)
J. Appl. Clin. Pediatr.
, vol.4
, pp. 025
-
-
Yu-Jiea, L.1
Yin-Nanb, M.2
Zu-Geng, C.3
Gua, T.4
Li-Ping, Z.5
Fang, F.6
-
162
-
-
77956335164
-
Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy
-
Zhang, C., Wong, V., Ng, P.W., Lui, C.H.T., Sin, N.C., Wong, K.S., Baum, L., and Kwan, P. (2010). Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy. Epilepsia 51, 1878-1881.
-
(2010)
Epilepsia
, vol.51
, pp. 1878-1881
-
-
Zhang, C.1
Wong, V.2
Ng, P.W.3
Lui, C.H.T.4
Sin, N.C.5
Wong, K.S.6
Baum, L.7
Kwan, P.8
-
163
-
-
84896778898
-
Association of febrile seizures and human myo-inositol monophosphatase 2 gene
-
Zhao, F., Liu, X.-m., Ke, X.-y., Ming, M., Gui, W.-x., Zhao, D.-c., Wang, D.-b. (2010). Association of febrile seizures and human myo-inositol monophosphatase 2 gene. J. Appl. Clin. Pediatr. 12, 017.
-
(2010)
J. Appl. Clin. Pediatr.
, vol.12
, pp. 017
-
-
Zhao, F.1
Liu, X.-M.2
Ke, X.-Y.3
Ming, M.4
Gui, W.-X.5
Zhao, D.-C.6
Wang, D.-B.7
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