-
1
-
-
34447312716
-
Idiosyncratic adverse reactions to antiepileptic drugs
-
Zaccara G, Franciotta D, Perucca E. Idiosyncratic adverse reactions to antiepileptic drugs. Epilepsia 2007; 48:1223-1244.
-
(2007)
Epilepsia
, vol.48
, pp. 1223-1244
-
-
Zaccara, G.1
Franciotta, D.2
Perucca, E.3
-
2
-
-
0032748789
-
Concordanceofprimarygeneral-ised epilepsy and carbamazepine hypersensitivity in monozygotic twins
-
EdwardsSG,HubbardV,AylettS,WrenD.Concordanceofprimarygeneral-ised epilepsy and carbamazepine hypersensitivity in monozygotic twins. Postgrad Med 1999; 75:680-681.
-
(1999)
Postgrad Med
, vol.75
, pp. 680-681
-
-
Edwards, S.G.1
Hubbard, V.2
Aylett, S.3
Wren, D.4
-
3
-
-
0035836342
-
TNF-a promoter region gene polymorphisms in carbamazepine hypersensitive patients
-
Pirmohamed M, Lin K, Chadwick D, Park K. TNF-a promoter region gene polymorphisms in carbamazepine hypersensitive patients. Neurology 2001; 56:890-896.
-
(2001)
Neurology
, vol.56
, pp. 890-896
-
-
Pirmohamed, M.1
Lin, K.2
Chadwick, D.3
Park, K.4
-
4
-
-
33645065133
-
Serious carbamazepine-induced hypersensitivity reactions associated with the HSP70 gene cluster
-
Alfirevic A, Mills T, Harrington P, et al. Serious carbamazepine-induced hypersensitivity reactions associated with the HSP70 gene cluster. Pharmacogenet Genomics 2006; 16:287-296.
-
(2006)
Pharmacogenet Genomics
, vol.16
, pp. 287-296
-
-
Alfirevic, A.1
Mills, T.2
Harrington, P.3
-
5
-
-
1842784823
-
Medicalgenetics:Amarkerforstevens-Johnson syndrome
-
ChungWH,HungSI,HongHS, et al. Medicalgenetics:amarkerforStevens-Johnson syndrome. Nature 2004; 428:486.
-
(2004)
Nature
, vol.428
, pp. 486
-
-
Chung, W.H.1
Hung, S.I.2
Hong, H.S.3
-
6
-
-
33645082244
-
Geneticsusceptibilitytocarbamazepine inducedcutaneousadversedrugreactions
-
HungSI,ChungWH,JeeSH, et al. Geneticsusceptibilitytocarbamazepine inducedcutaneousadversedrugreactions.PharmacogenetGenomics2006; 16:297-306.
-
(2006)
Pharmacogenet Genomics
, vol.16
, pp. 297-306
-
-
Hung, S.I.1
Chung, W.H.2
Jee, S.H.3
-
7
-
-
34248589506
-
Association between HLA-B 1502 allele andantiepilepticdrug- inducedcutaneousreactionsinHanChinese
-
Man CB, Kwan P, Baum L, et al. Association between HLA-B 1502 allele andantiepilepticdrug-inducedcutaneousreactionsinHanChinese.Epilepsia 2007; 48:1015-1018.
-
(2007)
Epilepsia
, vol.48
, pp. 1015-1018
-
-
Man, C.B.1
Kwan, P.2
Baum, L.3
-
8
-
-
57449118501
-
Carbamazepine andphenytoin inducedStevens-Johnsonsyndromeisassociatedwith HLA-B 1502 allelein Thai population
-
LocharernkulC, Loplumlert J,Limotai C, et al. Carbamazepine andphenytoin inducedStevens-Johnsonsyndromeisassociatedwith HLA-B 1502 allelein Thai population. Epilepsia 2008; 49:2087-2091.
-
(2008)
Epilepsia
, vol.49
, pp. 2087-2091
-
-
Locharernkul, C.1
Loplumlert, J.2
Limotai, C.3
-
9
-
-
33748987340
-
HLA-B locus in Caucasian patients with carbamazepine hypersensitivity
-
Alfirevic A, Jorgensen AL, Williamson PR, et al. HLA-B locus in Caucasian patients with carbamazepine hypersensitivity. Pharmacogenomics 2006; 7:813-818.
-
(2006)
Pharmacogenomics
, vol.7
, pp. 813-818
-
-
Alfirevic, A.1
Jorgensen, A.L.2
Williamson, P.R.3
-
10
-
-
33646934721
-
A marker for Stevens-Johnson syndrome ethnicity matters
-
Lonjou C, Thomas L, Borot N, et al. A marker for Stevens-Johnson syndrome . . .: ethnicity matters. Pharmacogenomics J 2006; 6:265-268.
-
(2006)
Pharmacogenomics J
, vol.6
, pp. 265-268
-
-
Lonjou, C.1
Thomas, L.2
Borot, N.3
-
11
-
-
38149108354
-
A European study of HLA-Bin Stevens-Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs
-
LonjouC,BorotaN,SekulaeP, et al. AEuropeanstudyofHLA-BinStevens-Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs. Pharmacogenet Genomics 2008; 18:99-107.
-
(2008)
Pharmacogenet Genomics
, vol.18
, pp. 99-107
-
-
Lonjou, C.1
Borota, N.2
Sekulae, P.3
-
12
-
-
61549115662
-
HLA-B locus in Japanese patients with antiepileptics and allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis
-
Kaniwa N, Saito Y, Aihara M, et al. HLA-B locus in Japanese patients with antiepileptics and allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis. Pharmacogenomics 2008; 9:1617-1622.
-
(2008)
Pharmacogenomics
, vol.9
, pp. 1617-1622
-
-
Kaniwa, N.1
Saito, Y.2
Aihara, M.3
-
14
-
-
37649006062
-
Investigation into the multidimensional genetic basis of drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis
-
Pirmohamed M, Arbuckle JB, Bowman CE, et al. Investigation into the multidimensional genetic basis of drug-induced Stevens-Johnson syndrome and toxic epidermal necrolysis. Pharmacogenomics 2007; 8:1661-1691.
-
(2007)
Pharmacogenomics
, vol.8
, pp. 1661-1691
-
-
Pirmohamed, M.1
Arbuckle, J.B.2
Bowman, C.E.3
-
16
-
-
58149257930
-
The clinical impact of pharma-cogeneticson the treatment of epilepsy
-
[Epub a head of print]
-
Löscher W, Klotz U, Zimprich F, Schmidt D. The clinical impact of pharma-cogeneticsonthetreatmentofepilepsy.Epilepsia2008[Epubaheadofprint].
-
(2008)
Epilepsia
-
-
Löscher, W.1
Klotz, U.2
Zimprich, F.3
Schmidt, D.4
-
17
-
-
38049168734
-
HLA-A, -B, -C, -DRB1 and -DQB1 alleles and haplotypes in the Kinh population in Vietnam
-
Hoa BK, Hang NT, Kashiwase K, et al. HLA-A, -B, -C, -DRB1 and -DQB1 alleles and haplotypes in the Kinh population in Vietnam. Tissue Antigens 2008; 71:127-134.
-
(2008)
Tissue Antigens
, vol.71
, pp. 127-134
-
-
Hoa, B.K.1
Hang, N.T.2
Kashiwase, K.3
-
18
-
-
34247366028
-
HLA haplotypes in Singapore: A study of mothers and their cord blood units
-
Tang TF, Hou L, Chen M, et al. HLA haplotypes in Singapore: a study of mothers and their cord blood units. Human Immunol 2007; 68:430-438.
-
(2007)
Human Immunol
, vol.68
, pp. 430-438
-
-
Tang, T.F.1
Hou, L.2
Chen, M.3
-
19
-
-
67650349868
-
Association of HLA-B 1502 allele and carbama-zepine-induced severe adverse cutaneous drug reaction among Asians, a review
-
Lim KS, Kwan P, Tan CT. Association of HLA-B 1502 allele and carbama-zepine-induced severe adverse cutaneous drug reaction among Asians, a review. Neurology Asia 2008; 13:15-21.
-
(2008)
Neurology Asia
, vol.13
, pp. 15-21
-
-
Lim, K.S.1
Kwan, P.2
Tan, C.T.3
-
20
-
-
51749101703
-
Balancing selection and heterogeneity across the classical human leukocyte antigen loci: A meta-analytic review of 497 population studies
-
Solberg OD, Mack SJ, Lancaster AK, et al. Balancing selection and heterogeneity across the classical human leukocyte antigen loci: a meta-analytic review of 497 population studies. Human Immunol 2008; 69:443-464.
-
(2008)
Human Immunol
, vol.69
, pp. 443-464
-
-
Solberg, O.D.1
MacK, S.J.2
Lancaster, A.K.3
-
21
-
-
55449105260
-
Carbamazepine, HLA-B 1502 and risk of Stevens-Johnson syndrome and toxic epidermal necrolysis: US FDA recommendations
-
FerrellPBJr,McLeodHL.Carbamazepine,HLA-B 1502andriskofStevens-Johnson syndrome and toxic epidermal necrolysis: US FDA recommendations. Pharmacogenomics 2008; 9:1543-1546.
-
(2008)
Pharmacogenomics
, vol.9
, pp. 1543-1546
-
-
Ferrell Jr., P.B.1
McLeod, H.L.2
-
22
-
-
33645060850
-
HLA-B genotyping to detect carbamaze-pine-inducedStevens-Johnsonsyndrome: Implicationsforpersonalizingmed-icine
-
Hung S-I, Chung W-H, Chen Y-T. HLA-B genotyping to detect carbamaze-pine-inducedStevens-Johnsonsyndrome:implicationsforpersonalizingmed- icine. Personalized Med 2005; 2:225-237.
-
(2005)
Personalized Med
, vol.2
, pp. 225-237
-
-
Hung, S.-I.1
Chung, W.-H.2
Chen, Y.-T.3
-
23
-
-
67649687833
-
Oxcarbazepine-induced Stevens-Johnson syndrome in a patient with HLA-B 1502 genotype
-
[Epub ahead of print]. doi: 10.1111/j.1468-3083.2008.02988.x
-
Chen Y-C, Chu C-Y, Hsiao C-H. Oxcarbazepine-induced Stevens-Johnson syndrome in a patient with HLA-B*1502 genotype. J Eur Acad Dermat Venereol 2008 [Epub ahead of print]. doi: 10.1111/j.1468-3083.2008.02988.x.
-
(2008)
J Eur Acad Dermat Venereol
-
-
Chen, Y.-C.1
Chu, C.-Y.2
Hsiao, C.-H.3
-
24
-
-
70349221352
-
-
U.S. Food and Drug Administration. Alter 24 Nov Accessed December 15, 2008
-
U.S. Food and Drug Administration.Phenytoinand fosphenytoin information. FDA Alter 24 Nov 2008. http://www.fda.gov/CDER/drug/infopage/pheny-toin- fosphenytoin/default.htm. [Accessed December 15, 2008]
-
(2008)
Phenytoinand Fosphenytoin Information
-
-
-
25
-
-
34248582562
-
Glutathione S-transferase M1 nullgenotypeas a risk factor for carbamazepine-induced mild hepatotoxicity
-
UedaK,IshitsuT,SeoT, et al. Glutathione S-transferase M1 nullgenotypeas a risk factor for carbamazepine-induced mild hepatotoxicity. Pharmacoge-nomics 2007; 8:435-442.
-
(2007)
Pharmacogenomics
, vol.8
, pp. 435-442
-
-
Ueda K.Ishitsu, T.1
Seo, T.2
-
26
-
-
38649130645
-
Glutathione S-transferase (GST) M1 null genotype and combined GSTM1 and GSTT1 null genotypes are risk factors for increased serum g-glutamyltransferase in valproic acid-treated patients
-
FukushimaY,SeoT,HashimotoN, et al. Glutathione S-transferase (GST) M1 null genotype and combined GSTM1 and GSTT1 null genotypes are risk factors for increased serum g-glutamyltransferase in valproic acid-treated patients. Clin Chim Acta 2008; 389:98-102.
-
(2008)
Clin Chim Acta
, vol.389
, pp. 98-102
-
-
Fukushima, Y.1
Seo, T.2
Hashimoto, N.3
-
27
-
-
0027973087
-
Severe hepatotoxicity during valproate therapy: An update and report of eight new fatalities
-
König SA, Siemes H, Bläker F, et al. Severe hepatotoxicity during valproate therapy: an update and report of eight new fatalities. Epilepsia 1994; 35:1005-1015.
-
(1994)
Epilepsia
, vol.35
, pp. 1005-1015
-
-
König, S.A.1
Siemes, H.2
Bläker, F.3
-
28
-
-
43149094182
-
Valproicacidmetabolismanditseffectson mitochondrial fatty acid oxidation: A review
-
[Epub ahead of print]
-
SilvaMF,AiresCC,LuisPB, et al. Valproicacidmetabolismanditseffectson mitochondrial fatty acid oxidation: a review. J Inherit Metab Dis 2008 [Epub ahead of print].
-
(2008)
J Inherit Metab Dis
-
-
Silva, M.F.1
Aires, C.C.2
Luis, P.B.3
-
29
-
-
33745713884
-
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene
-
Horvath R, Hudson G, Ferrari G, et al. Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Brain 2006; 129:1674-1684.
-
(2006)
Brain
, vol.129
, pp. 1674-1684
-
-
Horvath, R.1
Hudson, G.2
Ferrari, G.3
-
30
-
-
33745685519
-
The spectrum of clinical disease caused by the A467T and W748S POLG mutations: A study of 26 cases
-
Tzoulis C, Engelsen BA, Telstad W, et al. The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases. Brain 2006; 129:1685-1692.
-
(2006)
Brain
, vol.129
, pp. 1685-1692
-
-
Tzoulis, C.1
Engelsen, B.A.2
Telstad, W.3
-
31
-
-
38849125647
-
Reversiblevalproatehepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1)
-
McFarlandR,HudsonG,TaylorRW, et al. Reversiblevalproatehepatotoxicity due to mutations in mitochondrial DNA polymerase gamma (POLG1). Arch Dis Child 2008; 93:151-153.
-
(2008)
Arch Dis Child
, vol.93
, pp. 151-153
-
-
McFarland, R.1
Hudson, G.2
Taylor, R.W.3
-
32
-
-
33847632882
-
Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA
-
Lin CM, Thajeb P. Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA. Metab Brain Dis 2007; 22:105-109.
-
(2007)
Metab Brain Dis
, vol.22
, pp. 105-109
-
-
Lin, C.M.1
Thajeb, P.2
-
33
-
-
33750990215
-
Brain pseudoatrophy and mental regressiononvalproateandamitochondrialDNAmutation
-
Galimberti CA, Diegoli M, Sartori I, et al. Brain pseudoatrophy and mental regressiononvalproateandamitochondrialDNAmutation.Neurology2006; 67:1715-1717.
-
(2006)
Neurology
, vol.67
, pp. 1715-1717
-
-
Galimberti, C.A.1
Diegoli, M.2
Sartori, I.3
-
34
-
-
38549136786
-
Translocation-positive acute myeloidleukemiaassociatedwithvalproicacidtherapy
-
Williams DC Jr, Massey GV, Russell EC, et al. Translocation-positive acute myeloidleukemiaassociatedwithvalproicacidtherapy.PediatrBloodCancer 2008; 50:641-643.
-
(2008)
Pediatr Blood Cancer
, vol.50
, pp. 641-643
-
-
Jr W.Dc1
Massey, G.V.2
Russell, E.C.3
-
35
-
-
34447330490
-
Vigabatrin and epilepsy: Lessons learned
-
Wild JM, Ahn HS, Baulac M, et al. Vigabatrin and epilepsy: lessons learned. Epilepsia 2007; 48:1318-1327.
-
(2007)
Epilepsia
, vol.48
, pp. 1318-1327
-
-
Wild, J.M.1
Ahn, H.S.2
Baulac, M.3
-
36
-
-
33746873754
-
A pharmacogenetic exploration of vigabatrin- inducedvisualfieldconstriction
-
Kinirons P, Cavalleri GL, Singh R, et al. A pharmacogenetic exploration of vigabatrin-inducedvisualfieldconstriction.EpilepsyRes2006;70:144-152.
-
(2006)
Epilepsy Res
, vol.70
, pp. 144-152
-
-
Kinirons, P.1
Cavalleri, G.L.2
Singh, R.3
-
37
-
-
34250837645
-
Teratogenicity of antiepileptic drugs: Role of drug metabolism and pharmacogenomics
-
Sankar R. Teratogenicity of antiepileptic drugs: role of drug metabolism and pharmacogenomics. Acta Neurol Scand 2007; 116:65-71.
-
(2007)
Acta Neurol Scand
, vol.116
, pp. 65-71
-
-
Sankar, R.1
-
39
-
-
34547642309
-
Antiepilepticmedication during pregnancy: Does fetal genotype affect outcome?
-
AtkinsonDE,SophieBrice-BennettS,D'SouzaSW.Antiepilepticmedication during pregnancy: does fetal genotype affect outcome? Pediatr Res 2007; 62:120-127.
-
(2007)
Pediatr Res
, vol.62
, pp. 120-127
-
-
Atkinson, D.E.1
Sophie Brice-Bennett, S.2
D'Souza, S.W.3
-
40
-
-
0034190659
-
5,10-Methylenetetrahydrofolatereductasegenevariantsand congenital anomalies: A HuGE review
-
BottoLD,YangQ.5,10-Methylenetetrahydrofolatereductasegenevariantsand congenital anomalies: a HuGE review. Am J Epidemiol 2000; 151:862-877.
-
(2000)
Am J Epidemiol
, vol.151
, pp. 862-877
-
-
Botto, L.D.1
Yang, Q.2
-
41
-
-
0032718084
-
Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene
-
Dean JC, Moore SJ, Osborne A, et al. Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene. Clin Genet 1999; 56:216-220.
-
(1999)
Clin Genet
, vol.56
, pp. 216-220
-
-
Dean, J.C.1
Moore, S.J.2
Osborne, A.3
-
42
-
-
34848830461
-
Fetal anticonvulsant syndromes and polymorphisms in MTHFR, MTR, and MTRR
-
Dean J, Robertson Z, Reid V, et al. Fetal anticonvulsant syndromes and polymorphisms in MTHFR, MTR, and MTRR. Am J Med Genet A 2007; 143A:2303-2311.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 2303-2311
-
-
Dean, J.1
Robertson, Z.2
Reid, V.3
-
43
-
-
40049098652
-
AhighfrequencyoftheMTHFR677C>T polymorphisminScottishwomenwithepilepsy: Possibleroleinpathogenesis
-
DeanJC,RobertsonZ,ReidV, et al. AhighfrequencyoftheMTHFR677C>T polymorphisminScottishwomenwithepilepsy:possibleroleinpathogenesis. Seizure 2008; 17:269-275.
-
(2008)
Seizure
, vol.17
, pp. 269-275
-
-
Dean, J.C.1
Robertson, Z.2
Reid, V.3
-
44
-
-
36348976549
-
Influence of the MTHFR genotypeontherate of malformations following exposure to antiepileptic drugs in utero
-
KiniU, LeeR,JonesA, et al. Influence ofthe MTHFR genotypeontherate of malformations following exposure to antiepileptic drugs in utero. Eur J Med Genet 2007; 50:411-420.
-
(2007)
Eur J Med Genet
, vol.50
, pp. 411-420
-
-
Kini, U.1
Lee, R.2
Jones, A.3
|