-
1
-
-
0001925706
-
Benzodiazepines-Clobazam
-
R.H. Levy, R.H. Mattson, Meldrum B.S. 4th ed. New York, NY: Raven Press
-
Shorvon S.D. Benzodiazepines-Clobazam. Levy R.H., Mattson R.H., Meldrum B.S. 4th ed. Antiepileptic drugs. 1995;763-777 Raven Press, New York, NY.
-
(1995)
Antiepileptic Drugs
, pp. 763-777
-
-
Shorvon, S.D.1
-
2
-
-
0028846622
-
Treatment of electrical status epilepticus by short diazepam (DZP) cycles after DZP rectal bolus test
-
De Negri M., Baglietto M.G., Battaglia F.M., Gaggero R., Pessagno A., Recanati L. Treatment of electrical status epilepticus by short diazepam (DZP) cycles after DZP rectal bolus test. Brain Dev. 17:1995;330-333.
-
(1995)
Brain Dev
, vol.17
, pp. 330-333
-
-
De Negri, M.1
Baglietto, M.G.2
Battaglia, F.M.3
Gaggero, R.4
Pessagno, A.5
Recanati, L.6
-
3
-
-
0345899000
-
Modificazioni psicopatologiche indotte dai farmaci antiepilettici
-
Lega Italiana Contro l'Epilessia (LICE) Padova: Piccin "Nuova Libraria"
-
Viani F. Modificazioni psicopatologiche indotte dai farmaci antiepilettici. Lega Italiana Contro l'Epilessia (LICE). Manuale italiano di epilettologia. 1992;1397-1407 Piccin "Nuova Libraria" Padova.
-
(1992)
Manuale Italiano di Epilettologia
, pp. 1397-1407
-
-
Viani, F.1
-
4
-
-
0025744745
-
Monitoring of concentrations of clobazam and norclobazam in serum and saliva of children with epilepsy
-
Bardy A.H., Seppala T., Salokorpi T., Granstrom M.L., Santavuori P. Monitoring of concentrations of clobazam and norclobazam in serum and saliva of children with epilepsy. Brain Dev. 13:1991;174-179.
-
(1991)
Brain Dev
, vol.13
, pp. 174-179
-
-
Bardy, A.H.1
Seppala, T.2
Salokorpi, T.3
Granstrom, M.L.4
Santavuori, P.5
-
5
-
-
0032750843
-
Effect of felbamate on clobazam and its metabolite kinetics in patients with epilepsy
-
Contin M., Riva R., Albani F., Baruzzi A. Effect of felbamate on clobazam and its metabolite kinetics in patients with epilepsy. Ther Drug Monit. 21:1999;604-608.
-
(1999)
Ther Drug Monit
, vol.21
, pp. 604-608
-
-
Contin, M.1
Riva, R.2
Albani, F.3
Baruzzi, A.4
-
7
-
-
0034792584
-
Clinical relevance of genetic polymorphisms in the human CYP2C subfamily
-
Goldstein J.A. Clinical relevance of genetic polymorphisms in the human CYP2C subfamily. Br J Clin Pharmacol. 52:2001;349-355.
-
(2001)
Br J Clin Pharmacol
, vol.52
, pp. 349-355
-
-
Goldstein, J.A.1
-
8
-
-
0028260641
-
The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans
-
de Morais S.M., Wilkinson G.R., Blaisdell J., Nakamura K., Meyer U.A., Goldstein J.A. The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans. J Biol Chem. 269:1994;15419-15422.
-
(1994)
J Biol Chem
, vol.269
, pp. 15419-15422
-
-
De Morais, S.M.1
Wilkinson, G.R.2
Blaisdell, J.3
Nakamura, K.4
Meyer, U.A.5
Goldstein, J.A.6
-
9
-
-
0028044085
-
Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese
-
de Morais S.M., Wilkinson G.R., Blaisdell J., Meyer U.A., Nakamura K., Goldstein J.A. Identification of a new genetic defect responsible for the polymorphism of (S)-mephenytoin metabolism in Japanese. Mol Pharmacol. 46:1994;594-598.
-
(1994)
Mol Pharmacol
, vol.46
, pp. 594-598
-
-
De Morais, S.M.1
Wilkinson, G.R.2
Blaisdell, J.3
Meyer, U.A.4
Nakamura, K.5
Goldstein, J.A.6
-
10
-
-
15444340367
-
A new genetic defect in human CYP2C19: Mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin
-
Ferguson R.J., de Morais S.M., Benhamou S., et al. A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin. J Pharmacol Exp Ther. 284:1998;356-361.
-
(1998)
J Pharmacol Exp Ther
, vol.284
, pp. 356-361
-
-
Ferguson, R.J.1
De Morais, S.M.2
Benhamou, S.3
-
11
-
-
15644372745
-
An additional defective allele, CYP2C19*5, contributes to the S-mephenytoin poor metabolizer phenotype in Caucasians
-
Ibeanu G.C., Blaisdell J., Ghanayem B.I., et al. An additional defective allele, CYP2C19*5, contributes to the S-mephenytoin poor metabolizer phenotype in Caucasians. Pharmacogenetics. 8:1998;129-135.
-
(1998)
Pharmacogenetics
, vol.8
, pp. 129-135
-
-
Ibeanu, G.C.1
Blaisdell, J.2
Ghanayem, B.I.3
-
12
-
-
0032159423
-
Identification of new human CYP2C19 alleles (CYP2C19*6 and CYP2C19*2B) in a Caucasian poor metabolizer of mephenytoin
-
Ibeanu G.C., Goldstein J.A., Meyer U., et al. Identification of new human CYP2C19 alleles (CYP2C19*6 and CYP2C19*2B) in a Caucasian poor metabolizer of mephenytoin. J Pharmacol Exp Ther. 286:1998;1490-1495.
-
(1998)
J Pharmacol Exp Ther
, vol.286
, pp. 1490-1495
-
-
Ibeanu, G.C.1
Goldstein, J.A.2
Meyer, U.3
-
13
-
-
0033020057
-
Landau-Kleffner syndrome (LKS): Long-term follow-up and links with electrical status epilepticus during sleep (ESES)
-
Giovanardi Rossi P., Parmeggiani A., Posar A., Scaduto M.C., Chiodo S., Vatti G. Landau-Kleffner syndrome (LKS): long-term follow-up and links with electrical status epilepticus during sleep (ESES). Brain Dev. 21:1999;90-98.
-
(1999)
Brain Dev
, vol.21
, pp. 90-98
-
-
Giovanardi Rossi, P.1
Parmeggiani, A.2
Posar, A.3
Scaduto, M.C.4
Chiodo, S.5
Vatti, G.6
|