Artículos de revistas
Familial Partial Epilepsies [epilepsias Parciais Familiares]
Registro en:
Arquivos De Neuro-psiquiatria. , v. 58, n. 3 B, p. 862 - 868, 2000.
0004282X
2-s2.0-0034276588
Autor
Kobayashi E.
Cendes F.
Sousa S.C.
Scotoni A.E.
Carvalho M.I.
Guerreiro M.M.
Guerreiro C.A.M.
Lopes-Cendes I.
Institución
Resumen
[No abstract available] 58 3 B 862 868 Ottmann, R., Lee, J.H., Risch, N., Clinical indicators of genetic susceptibility to epilepsy (1996) Epilepsia, 37, pp. 353-361 Hauser, W.A., Anderson, V.E., Genetics of epilepsy (1986) Recent Advances in Epilepsy, 3, pp. 21-36. , Pedley TA. Meldrum BS. (eds). Edinburgh: Churchill Livingstone Andermann, E., Multifactorial inheritance of generalized and focal epilepsy (1982) Genetic Basis of the Epilepsies, pp. 355-374. , Anderson VE, Hauser WA, Penry JK, Sing CF (eds). New York: Raven Press Anneger, J.F., Hauser, W.A., Anderson, V.E., Risk of seizures among relatives of patients with epilepsy: Families in a defined population (1982) The Genetic Basis of the Epilepsies, pp. 151-159. , Anderson VE, Hauser WA, Sing L, Porter R (eds). New York: Raven Press Berkovic, S.F., Howell, R.A., Hay, D.A., Hopper, J.L., Epilepsies in twins: Genetics of the major epilepsy syndromes (1998) Ann Neurol, 43, pp. 435-445 Ottman, R., Genetics of the partial epilepsies: A review (1989) Epilepsia, 30, pp. 107-111 Phillips, H.A., Scheffer, I.E., Berkovic, S.F., Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2 (1995) Nat Genet, 10, pp. 5117-5118 Ottman, R., Risch, N., Hauser, W.A., Localization of a gene for partial epilepsy to chromosome 10q (1995) Nat Genet, 10, pp. 56-60 Scheffer, I.E., Phillips, H.A., O'Brien, C.E., Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2 (1998) Ann Neurol, 44, pp. 890-899 Cendes, F., Lopes-Cendes, I., Andermann, E., Andermann, F., Familial temporal lobe epilepsy: A clinically heterogeneous syndrome (1998) Neurology, 50, pp. 554-557 Berkovic, S.F., Scheffer, I.E., Genetics of the epilepsies (1999) Curr Opin Neurol, 12, pp. 177-182 Bievert, C., Schoeder, B.C., Kubisch, C., Berkovic, S.F., Propping, P., Jentsch, T.J., Steinlein, O.K., A potassium channel mutation in neonatal human epilepsy (1998) Science, 279, pp. 403-406 Singh, N.A., Charlier, C., Stauffer, D., A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns (1998) Nat Genet, 18, pp. 25-29 Steinlein, O.K., Mulley, J.C., Propping, P., A missense mutation in the neuronal nicotinic acetylcholine receptor a4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy (1995) Nature Genet, 11, pp. 201-203 Wallace, R.H., Wang, D.W., Sing, R., Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCNIB (1998) Nat Genet, 19, pp. 366-370 Proposal for a revised classification of epilepsies and epileptic syndromes (1989) Epilepsia, 30, pp. 389-399 Aicardi, J., Epileptic syndromes in childhood (1988) Epilepsia, 29 (3 SUPPL.), pp. S1-S5