-
2
-
-
0023272497
-
Concepts of absence epilepsies: Discrete syndrome or biological continuum?
-
Berkovic SF, Andermann F, Andermann E, et al. Concepts of absence epilepsies: discrete syndrome or biological continuum? Neurology 1987;37:993-1000.
-
(1987)
Neurology
, vol.37
, pp. 993-1000
-
-
Berkovic, S.F.1
Andermann, F.2
Andermann, E.3
-
3
-
-
0008670355
-
Linkage analysis between subsyndromes of childhood absence epilepsy (CAE) and the GABAA receptor beta 3 subunit (GABRB3) on chromosome 15q11.2-q12
-
Tanaka M, Castroviejo IP, Medina MT, et al. Linkage analysis between subsyndromes of childhood absence epilepsy (CAE) and the GABAA receptor beta 3 subunit (GABRB3) on chromosome 15q11.2-q12. Epilepsia 2000;41(Suppl 7): 250.
-
(2000)
Epilepsia
, vol.41
, Issue.SUPPL. 7
, pp. 250
-
-
Tanaka, M.1
Castroviejo, I.P.2
Medina, M.T.3
-
4
-
-
18344384217
-
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q
-
Robinson R, Taske N, Sander T, et al. Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q. Epilepsy Res 2002;48:169-179.
-
(2002)
Epilepsy Res.
, vol.48
, pp. 169-179
-
-
Robinson, R.1
Taske, N.2
Sander, T.3
-
5
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch NJ. Searching for genetic determinants in the new millennium. Nature 2000;405:847-856.
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
6
-
-
0032849405
-
Possible association between childhood absence epilepsy and the gene encoding GABRB3
-
Feucht M, Fuchs K, Pichlbauer E, et al. Possible association between childhood absence epilepsy and the gene encoding GABRB3. Biol Psychiatry 1999;46:997-1002.
-
(1999)
Biol. Psychiatry
, vol.46
, pp. 997-1002
-
-
Feucht, M.1
Fuchs, K.2
Pichlbauer, E.3
-
7
-
-
0024317220
-
Commission on classification and terminology of the International League against Epilepsy: Proposal for revised classification of epilepsies and epileptic syndromes
-
Commission on classification and terminology of the International League against Epilepsy: proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 1989;30:389-399.
-
(1989)
Epilepsia
, vol.30
, pp. 389-399
-
-
-
8
-
-
0024284028
-
A simple saiting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dyhes DD, Poleskey HF, et al. A simple saiting out procedure for extracting DNA from human nucleated cells. Nucleic Acid Res 1988;16:1215.
-
(1988)
Nucleic Acid Res.
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dyhes, D.D.2
Poleskey, H.F.3
-
9
-
-
0028896579
-
Basic mechanism of generalized absence seizures
-
Snead OC III. Basic mechanism of generalized absence seizures. Ann Neurol 1995;37:146-157.
-
(1995)
Ann. Neurol.
, vol.37
, pp. 146-157
-
-
Snead III, O.C.1
-
10
-
-
0031887096
-
Mechanisms of generalized absence epilepsy
-
Futatsugi Y, Riviello JJ. Mechanisms of generalized absence epilepsy. Brain Dev 1998;20:75-79.
-
(1998)
Brain Dev.
, vol.20
, pp. 75-79
-
-
Futatsugi, Y.1
Riviello, J.J.2
-
11
-
-
0031127105
-
Structure and organization of GABRB3 and GABRA5
-
Glatt K, Glatt H, Lalande M. Structure and organization of GABRB3 and GABRA5. Genomics 1997;41:63-39.
-
(1997)
Genomics
, vol.41
, pp. 39-63
-
-
Glatt, K.1
Glatt, H.2
Lalande, M.3
-
13
-
-
0027338179
-
GABAA receptor impairment in the genetic absence epilepsy rats from Strasbourg (GAERS): An immunocytochemical and receptor binding autoradiographic study
-
Spreafico R, Mennini T, Danober L, et al. GABAA receptor impairment in the genetic absence epilepsy rats from Strasbourg (GAERS): an immunocytochemical and receptor binding autoradiographic study. Epilepsy Res 1993;15:229-238.
-
(1993)
Epilepsy Res.
, vol.15
, pp. 229-238
-
-
Spreafico, R.1
Mennini, T.2
Danober, L.3
-
14
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander ES, Schork NJ. Genetic dissection of complex traits. Science 1994;265:2037-2048.
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
16
-
-
10744224470
-
Mutation screen of the gene encoding GABRB3 in Chinese patients with childhood absence epilepsy
-
Lu J, Pan H, Chen Y, et al. Mutation screen of the gene encoding GABRB3 in Chinese patients with childhood absence epilepsy. Am J Med Genet 2003;123A:197-200.
-
(2003)
Am. J. Med. Genet.
, vol.123 A
, pp. 197-200
-
-
Lu, J.1
Pan, H.2
Chen, Y.3
|