-
1
-
-
79951819917
-
PLA2R autoantibodies and PLA2R glomerular deposits inmembranous nephropathy
-
Debiec H, Ronco P: PLA2R autoantibodies and PLA2R glomerular deposits inmembranous nephropathy. NEngl JMed 364: 689-690, 2011
-
(2011)
NEngl JMed
, vol.364
, pp. 689-690
-
-
Debiec, H.1
Ronco, P.2
-
2
-
-
79957745793
-
Antiphospholipase A2 receptor antibody in membranous nephropathy
-
Qin W, Beck LH Jr., Zeng C, Chen Z, Li S, Zuo K, Salant DJ, Liu Z: Antiphospholipase A2 receptor antibody in membranous nephropathy. J Am Soc Nephrol 22: 1137-1143, 2011
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 1137-1143
-
-
Qin, W.1
Beck, L.H.2
Zeng, C.3
Chen, Z.4
Li, S.5
Zuo, K.6
Salant, D.J.7
Liu, Z.8
-
3
-
-
84859007767
-
Pathogenesis ofmembranous nephropathy: Recent advances and future challenges
-
Ronco P, DebiecH: Pathogenesis ofmembranous nephropathy: Recent advances and future challenges. Nat Rev Nephrol 8: 203-213, 2012
-
(2012)
Nat Rev Nephrol
, vol.8
, pp. 203-213
-
-
Ronco, P.1
Debiec, H.2
-
4
-
-
84921470210
-
Molecular mechanisms for contribution of MHC molecules to autoimmune diseases
-
Sollid LM, Pos W, Wucherpfennig KW: Molecular mechanisms for contribution of MHC molecules to autoimmune diseases. Curr Opin Immunol 31: 24-30, 2014
-
(2014)
Curr Opin Immunol
, vol.31
, pp. 24-30
-
-
Sollid, L.M.1
Pos, W.2
Wucherpfennig, K.W.3
-
5
-
-
84875700090
-
Genetic variants in membranous nephropathy: Perhaps a perfect storm rather than a straightforward conformeropathy?
-
Salant DJ: Genetic variants in membranous nephropathy: Perhaps a perfect storm rather than a straightforward conformeropathy? JAmSoc Nephrol 24: 525-528, 2013
-
(2013)
JAmSoc Nephrol
, vol.24
, pp. 525-528
-
-
Salant, D.J.1
-
6
-
-
0024802692
-
A DQA1 allele is strongly associated with idiopathic membranous nephropathy
-
Vaughan RW, Demaine AG, Welsh KI: A DQA1 allele is strongly associated with idiopathic membranous nephropathy. Tissue Antigens 34: 261-269, 1989
-
(1989)
Tissue Antigens
, vol.34
, pp. 261-269
-
-
Vaughan, R.W.1
Demaine, A.G.2
Welsh, K.I.3
-
7
-
-
0018697572
-
Strong association between idiopathic membranous nephropathy and HLA-DRW3
-
Klouda PT, Manos J, Acheson EJ, Dyer PA, Goldby FS, Harris R, Lawler W, Mallick NP, Williams G: Strong association between idiopathic membranous nephropathy and HLA-DRW3. Lancet 2: 770-771, 1979
-
(1979)
Lancet
, vol.2
, pp. 770-771
-
-
Klouda, P.T.1
Manos, J.2
Acheson, E.J.3
Dyer, P.A.4
Goldby, F.S.5
Harris, R.6
Lawler, W.7
Mallick, N.P.8
Williams, G.9
-
8
-
-
0026571118
-
Analysis of HLA class II genes in Japanese patients with idiopathic membranous glomerulonephritis
-
Ogahara S, Naito S, Abe K, Michinaga I, Arakawa K: Analysis of HLA class II genes in Japanese patients with idiopathic membranous glomerulonephritis. Kidney Int 41: 175-182, 1992
-
(1992)
Kidney Int
, vol.41
, pp. 175-182
-
-
Ogahara, S.1
Naito, S.2
Abe, K.3
Michinaga, I.4
Arakawa, K.5
-
9
-
-
85190326140
-
The susceptible human leukocyte antigen class II genes and the encoding amino acid residues on major histocompatibility complex molecules to primary membranous nephropathy [Abstract]
-
FR-PO159
-
Xie L-j, Qu Z, Cui Z, Liu G, Liao Y-h, Zhao M-h: The susceptible human leukocyte antigen class II genes and the encoding amino acid residues on major histocompatibility complex molecules to primary membranous nephropathy [Abstract]. J Am Soc Nephrol 26: 392A:FR-PO159, 2015
-
(2015)
J Am Soc Nephrol
, vol.26
, pp. 392A
-
-
L-J, X.1
Qu, Z.2
Cui, Z.3
Liu, G.4
Y-H, L.5
M-H, Z.6
-
10
-
-
85190321708
-
Interaction of risk alleles in Japanese idiopathic membranous nephropathy [Abstract]
-
SAPO502
-
Honda K, Thir M, Okamoto K, Doi K, Hodaka, Suzuki, Watanabe T, Nangaku M, Tokunaga K, Noiri E: Interaction of risk alleles in Japanese idiopathic membranous nephropathy [Abstract]. J AmSoc Nephrol 26: 739A26:SA-PO502, 2015
-
(2015)
J AmSoc Nephrol
, vol.26
, pp. 739A26
-
-
Honda, K.1
Thir, M.2
Okamoto, K.3
Doi, K.4
Hodaka, S.5
Watanabe, T.6
Nangaku, M.7
Tokunaga, K.8
Noiri, E.9
-
11
-
-
79951827439
-
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy
-
Stanescu HC, Arcos-Burgos M, Medlar A, Bockenhauer D, Kottgen A, Dragomirescu L, Voinescu C, Patel N, Pearce K, Hubank M, Stephens HA, Laundy V, Padmanabhan S, Zawadzka A, Hofstra JM, Coenen MJ, den Heijer M, Kiemeney LA, Bacq-Daian D, Stengel B, Powis SH, Brenchley P, Feehally J, Rees AJ, Debiec H, Wetzels JF, Ronco P, Mathieson PW, Kleta R: Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. N Engl JMed 364: 616-626, 2011
-
(2011)
N Engl JMed
, vol.364
, pp. 616-626
-
-
Stanescu, H.C.1
Arcos-Burgos, M.2
Medlar, A.3
Bockenhauer, D.4
Kottgen, A.5
Dragomirescu, L.6
Voinescu, C.7
Patel, N.8
Pearce, K.9
Hubank, M.10
Stephens, H.A.11
Laundy, V.12
Padmanabhan, S.13
Zawadzka, A.14
Hofstra, J.M.15
Coenen, M.J.16
Den Heijer, M.17
Kiemeney, L.A.18
Bacq-Daian, D.19
Stengel, B.20
Powis, S.H.21
Brenchley, P.22
Feehally, J.23
Rees, A.J.24
Debiec, H.25
Wetzels, J.F.26
Ronco, P.27
Mathieson, P.W.28
Kleta, R.29
more..
-
12
-
-
79957470331
-
Risk alleles in idiopathic membranous nephropathy
-
Kiryluk K: Risk alleles in idiopathic membranous nephropathy. NEngl J Med 364: 2072-2073, 2011
-
(2011)
NEngl J Med
, vol.364
, pp. 2072-2073
-
-
Kiryluk, K.1
-
13
-
-
84929590969
-
Pathophysiological advances in membranous nephropathy: Time for a shift in patient's care
-
Ronco P, Debiec H: Pathophysiological advances in membranous nephropathy: Time for a shift in patient's care. Lancet 385: 1983-1992, 2015
-
(2015)
Lancet
, vol.385
, pp. 1983-1992
-
-
Ronco, P.1
Debiec, H.2
-
14
-
-
0037182728
-
Antenatal membranous glomerulonephritis due to anti-neutral endopeptidase antibodies
-
Debiec H, Guigonis V, Mougenot B, Decobert F, Haymann JP, Bensman A, Deschênes G, Ronco PM: Antenatal membranous glomerulonephritis due to anti-neutral endopeptidase antibodies. N Engl J Med 346: 2053-2060, 2002
-
(2002)
N Engl J Med
, vol.346
, pp. 2053-2060
-
-
Debiec, H.1
Guigonis, V.2
Mougenot, B.3
Decobert, F.4
Haymann, J.P.5
Bensman, A.6
Deschênes, G.7
Ronco, P.M.8
-
15
-
-
84918548245
-
Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy
-
Tomas NM, Beck LH Jr., Meyer-Schwesinger C, Seitz-Polski B, Ma H, Zahner G, Dolla G, Hoxha E, Helmchen U, Dabert-Gay AS, Debayle D, Merchant M, Klein J, SalantDJ, Stahl RA, LambeauG: Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy. N Engl JMed 371: 2277-2287, 2014
-
(2014)
N Engl JMed
, vol.371
, pp. 2277-2287
-
-
Tomas, N.M.1
Beck, L.H.2
Meyer-Schwesinger, C.3
Seitz-Polski, B.4
Ma, H.5
Zahner, G.6
Dolla, G.7
Hoxha, E.8
Helmchen, U.9
Dabert-Gay, A.S.10
Debayle, D.11
Merchant, M.12
Klein, J.13
Salant, D.J.14
Stahl, R.A.15
Lambeau, G.16
-
16
-
-
85016049278
-
Genetic risk variants for membranous nephropathy: Extension of and association with other chronic kidney disease aetiologies
-
[published online ahead of print February 4, 2016], GCKD Investigators
-
Sekula P, Li Y, Stanescu HC, Wuttke M, Ekici AB, Bockenhauer D, Walz G, Powis SH, Kielstein JT, Brenchley P, Eckardt KU, Kronenberg F, Kleta R, Köttgen A, Köttgen A; GCKD Investigators: Genetic risk variants for membranous nephropathy: Extension of and association with other chronic kidney disease aetiologies [published online ahead of print February 4, 2016]. Nephrol Dial Transplant 10.1093/ndt/gfw1001
-
Nephrol Dial Transplant
-
-
Sekula, P.1
Li, Y.2
Stanescu, H.C.3
Wuttke, M.4
Ekici, A.B.5
Bockenhauer, D.6
Walz, G.7
Powis, S.H.8
Kielstein, J.T.9
Brenchley, P.10
Eckardt, K.U.11
Kronenberg, F.12
Kleta, R.13
Köttgen, A.14
Köttgen, A.15
-
17
-
-
84898786106
-
Statistical power and significance testing in largescale genetic studies
-
ShamPC, Purcell SM: Statistical power and significance testing in largescale genetic studies. Nat Rev Genet 15: 335-346, 2014
-
(2014)
Nat Rev Genet
, vol.15
, pp. 335-346
-
-
Sham, P.C.1
Purcell, S.M.2
-
18
-
-
84969786267
-
Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease
-
Zhou F, Cao H, Zuo X, Zhang T, Zhang X, Liu X, Xu R, Chen G, Zhang Y, Zheng X, Jin X, Gao J, Mei J, Sheng Y, Li Q, Liang B, Shen J, Shen C, Jiang H, Zhu C, Fan X, Xu F, YueM, Yin X, Ye C, Zhang C, Liu X, Yu L, Wu J, ChenM, Zhuang X, Tang L, Shao H, Wu L, Li J, Xu Y, Zhang Y, Zhao S, Wang Y, Li G, Xu H, Zeng L, Wang J, Bai M, Chen Y, Chen W, Kang T, Wu Y, Xu X, Zhu Z, Cui Y, Wang Z, Yang C, Wang P, Xiang L, Chen X, Zhang A, Gao X, Zhang F, Xu J, Zheng M, Zheng J, Zhang J, Yu X, Li Y, Yang S, YangH, Wang J, Liu J, HammarströmL, Sun L, Wang J, Zhang X: Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease. Nat Genet 48: 740-746, 2016
-
(2016)
Nat Genet
, vol.48
, pp. 740-746
-
-
Zhou, F.1
Cao, H.2
Zuo, X.3
Zhang, T.4
Zhang, X.5
Liu, X.6
Xu, R.7
Chen, G.8
Zhang, Y.9
Zheng, X.10
Jin, X.11
Gao, J.12
Mei, J.13
Sheng, Y.14
Li, Q.15
Liang, B.16
Shen, J.17
Shen, C.18
Jiang, H.19
Zhu, C.20
Fan, X.21
Xu, F.22
Yue, M.23
Yin, X.24
Ye, C.25
Zhang, C.26
Liu, X.27
Yu, L.28
Wu, J.29
Chen, M.30
Zhuang, X.31
Tang, L.32
Shao, H.33
Wu, L.34
Li, J.35
Xu, Y.36
Zhang, Y.37
Zhao, S.38
Wang, Y.39
Li, G.40
Xu, H.41
Zeng, L.42
Wang, J.43
Bai, M.44
Chen, Y.45
Chen, W.46
Kang, T.47
Wu, Y.48
Xu, X.49
Zhu, Z.50
Cui, Y.51
Wang, Z.52
Yang, C.53
Wang, P.54
Xiang, L.55
Chen, X.56
Zhang, A.57
Gao, X.58
Zhang, F.59
Xu, J.60
Zheng, M.61
Zheng, J.62
Zhang, J.63
Yu, X.64
Li, Y.65
Yang, S.66
Yang, H.67
Wang, J.68
Liu, J.69
Hammarström, L.70
Sun, L.71
Wang, J.72
Zhang, X.73
more..
-
19
-
-
84883798899
-
Six-locus high resolution HLA haplotype frequencies derived from mixed-resolutionDNA typing for the entire US donor registry
-
Gragert L, Madbouly A, Freeman J, MaiersM: Six-locus high resolution HLA haplotype frequencies derived from mixed-resolutionDNA typing for the entire US donor registry. Hum Immunol 74: 1313-1320, 2013
-
(2013)
Hum Immunol
, vol.74
, pp. 1313-1320
-
-
Gragert, L.1
Madbouly, A.2
Freeman, J.3
Maiers, M.4
-
20
-
-
84947747820
-
Highresolution analyses of human leukocyte antigens allele and haplotype frequencies based on 169, 995 volunteers fromthe China BoneMarrow Donor Registry Program
-
Zhou XY, Zhu FM, Li JP, Mao W, Zhang DM, Liu ML, Hei AL, Dai DP, Jiang P, Shan XY, Zhang BW, Zhu CF, Shen J, Deng ZH, Wang ZL, Yu WJ, ChenQ, Qiao YH, Zhu XM, Lv R, Li GY, Li GL, Li HC, Zhang X, Pei B, Jiao LX, Shen G, Liu Y, Feng ZH, Su YP, Xu ZX, DiWY, Jiang YQ, Fu HL, Liu XJ, Liu X, Zhou MZ, Du D, Liu Q, Han Y, Zhang ZX, Cai JP: Highresolution analyses of human leukocyte antigens allele and haplotype frequencies based on 169, 995 volunteers fromthe China BoneMarrow Donor Registry Program. PLoS One 10: E0139485, 2015
-
(2015)
PLoS One
, vol.10
, pp. e0139485
-
-
Zhou, X.Y.1
Zhu, F.M.2
Li, J.P.3
Mao, W.4
Zhang, D.M.5
Liu, M.L.6
Hei, A.L.7
Dai, D.P.8
Jiang, P.9
Shan, X.Y.10
Zhang, B.W.11
Zhu, C.F.12
Shen, J.13
Liu, Z.H.14
Wang, Z.L.15
Yu, W.J.16
Chen, Q.17
Qiao, Y.H.18
Zhu, X.M.19
Lv, R.20
Li, G.Y.21
Li, G.L.22
Li, H.C.23
Zhang, X.24
Pei, B.25
Jiao, L.X.26
Shen, G.27
Liu, Y.28
Zh, F.29
Su, Y.P.30
Xu, Z.X.31
Di, W.Y.32
Jiang, Y.Q.33
Fu, H.L.34
Liu, X.J.35
Liu, X.36
Zhou, M.Z.37
Du, D.38
Liu, Q.39
Han, Y.40
Zhang, Z.X.41
Cai, J.P.42
more..
-
21
-
-
80052740749
-
Next-generation genome-wide association studies: Time to focus on phenotype?
-
MacRae CA, Vasan RS: Next-generation genome-wide association studies: Time to focus on phenotype? Circ Cardiovasc Genet 4: 334-336, 2011
-
(2011)
Circ Cardiovasc Genet
, vol.4
, pp. 334-336
-
-
MacRae, C.A.1
Vasan, R.S.2
-
22
-
-
84885413003
-
The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases
-
ManchiaM, Cullis J, TureckiG, Rouleau GA, Uher R, AldaM: The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases. PLoS One 8: E76295, 2013
-
(2013)
PLoS One
, vol.8
, pp. e76295
-
-
Manchia, M.1
Cullis, J.2
Turecki, G.3
Rouleau, G.A.4
Uher, R.5
Alda, M.6
-
23
-
-
84880807131
-
An integrated tool to study MHC region: Accurate SNV detection and HLA genes typing in humanMHC region using targeted high-throughput sequencing
-
Cao H, Wu J, Wang Y, JiangH, Zhang T, Liu X, Xu Y, LiangD, Gao P, Sun Y, Gifford B, D'Ascenzo M, Liu X, Tellier LC, Yang F, Tong X, Chen D, Zheng J, Li W, Richmond T, Xu X, Wang J, Li Y: An integrated tool to study MHC region: Accurate SNV detection and HLA genes typing in humanMHC region using targeted high-throughput sequencing. PLoS One 8: E69388, 2013
-
(2013)
PLoS One
, vol.8
, pp. e69388
-
-
Cao, H.1
Wu, J.2
Wang, Y.3
Jiang, H.4
Zhang, T.5
Liu, X.6
Xu, Y.7
Liang, D.8
Gao, P.9
Sun, Y.10
Gifford, B.11
D'Ascenzo, M.12
Liu, X.13
Tellier, L.C.14
Yang, F.15
Tong, X.16
Chen, D.17
Zheng, J.18
Li, W.19
Richmond, T.20
Xu, X.21
Wang, J.22
Li, Y.23
more..
-
24
-
-
84938423979
-
Coeliac disease and rheumatoid arthritis: Similar mechanisms, different antigens
-
Koning F, Thomas R, Rossjohn J, Toes RE: Coeliac disease and rheumatoid arthritis: Similar mechanisms, different antigens. Nat Rev Rheumatol 11: 450-461, 2015
-
(2015)
Nat Rev Rheumatol
, vol.11
, pp. 450-461
-
-
Koning, F.1
Thomas, R.2
Rossjohn, J.3
Toes, R.E.4
-
25
-
-
84923919539
-
Identification of the immunodominant epitope region in phospholipase A2 receptor-mediating autoantibody binding in idiopathic membranous nephropathy
-
Kao L, Lam V, Waldman M, Glassock RJ, Zhu Q: Identification of the immunodominant epitope region in phospholipase A2 receptor-mediating autoantibody binding in idiopathic membranous nephropathy. J Am Soc Nephrol 26: 291-301, 2015
-
(2015)
J Am Soc Nephrol
, vol.26
, pp. 291-301
-
-
Kao, L.1
Lam, V.2
Waldman, M.3
Glassock, R.J.4
Zhu, Q.5
-
26
-
-
85015131433
-
Epitope spreading of autoantibody response to PLA2R associates with poor prognosis in membranous nephropathy
-
Seitz-Polski B, Dolla G, Payré C, Girard CA, Polidori J, Zorzi K, Birgy-Barelli E, Jullien P, Courivaud C, Krummel T, Benzaken S, Bernard G, Burtey S, Mariat C, Esnault VL, Lambeau G: Epitope spreading of autoantibody response to PLA2R associates with poor prognosis in membranous nephropathy. J Am Soc Nephrol 27: 1517-1533, 2016
-
(2016)
J Am Soc Nephrol
, vol.27
, pp. 1517-1533
-
-
Seitz-Polski, B.1
Dolla, G.2
Payré, C.3
Girard, C.A.4
Polidori, J.5
Zorzi, K.6
Birgy-Barelli, E.7
Jullien, P.8
Courivaud, C.9
Krummel, T.10
Benzaken, S.11
Bernard, G.12
Burtey, S.13
Mariat, C.14
Esnault, V.L.15
Lambeau, G.16
-
27
-
-
84875702300
-
Phospholipase A2 receptor (PLA2R1) sequence variants in idiopathic membranous nephropathy
-
CoenenMJ, Hofstra JM, Debiec H, Stanescu HC, Medlar AJ, Stengel B, Boland-Augé A, Groothuismink JM, Bockenhauer D, Powis SH, Mathieson PW, Brenchley PE, Kleta R, Wetzels JF, Ronco P: Phospholipase A2 receptor (PLA2R1) sequence variants in idiopathic membranous nephropathy. J Am Soc Nephrol 24: 677-683, 2013
-
(2013)
J Am Soc Nephrol
, vol.24
, pp. 677-683
-
-
Coenen, M.J.1
Hofstra, J.M.2
Debiec, H.3
Stanescu, H.C.4
Medlar, A.J.5
Stengel, B.6
Boland-Augé, A.7
Groothuismink, J.M.8
Bockenhauer, D.9
Powis, S.H.10
Mathieson, P.W.11
Brenchley, P.E.12
Kleta, R.13
Wetzels, J.F.14
Ronco, P.15
-
28
-
-
85011704961
-
Combined assessment of phospholipase A2 receptor autoantibodies and glomerular deposits in membranous nephropathy
-
Qin HZ, ZhangMC, LeWB, RenQ, ChenDC, Zeng CH, Liu L, Zuo K, Xu F, Liu ZH: Combined assessment of phospholipase A2 receptor autoantibodies and glomerular deposits in membranous nephropathy. J Am Soc Nephrol 27: 3195-3203, 2016
-
(2016)
J Am Soc Nephrol
, vol.27
, pp. 3195-3203
-
-
Qin, H.Z.1
Zhang, M.C.2
Le, W.B.3
Ren, Q.4
Chen, D.C.5
Ch, Z.6
Liu, L.7
Zuo, K.8
Xu, F.9
Zh, L.10
-
29
-
-
58849104457
-
The HLA genomic loci map: Expression, interaction, diversity and disease
-
Shiina T, Hosomichi K, Inoko H, Kulski JK: The HLA genomic loci map: Expression, interaction, diversity and disease. J Hum Genet 54: 15-39, 2009
-
(2009)
J Hum Genet
, vol.54
, pp. 15-39
-
-
Shiina, T.1
Hosomichi, K.2
Inoko, H.3
Kulski, J.K.4
-
30
-
-
9444295337
-
Gene map of the extended human MHC
-
HortonR, WilmingL, RandV, LoveringRC, BrufordEA, Khodiyar VK, LushMJ, Povey S, TalbotCCJr., WrightMW, WainHM, Trowsdale J, ZieglerA, Beck S: Gene map of the extended human MHC. Nat Rev Genet 5: 889-899, 2004
-
(2004)
Nat Rev Genet
, vol.5
, pp. 889-899
-
-
Horton, R.1
Wilming, L.2
Rand, V.3
Lovering, R.C.4
Bruford, E.A.5
Khodiyar, V.K.6
Lush, M.J.7
Povey, S.8
Talbot, C.C.9
Wright, M.W.10
Wain, H.M.11
Trowsdale, J.12
Ziegler, A.13
Beck, S.14
-
31
-
-
77956534324
-
ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data
-
Wang K, Li M, Hakonarson H: ANNOVAR: Functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 38: E164, 2010
-
(2010)
Nucleic Acids Res
, vol.38
, pp. e164
-
-
Wang, K.1
Li, M.2
Hakonarson, H.3
-
32
-
-
84886265139
-
HLA-B∗13:01 and the dapsone hypersensitivity syndrome
-
Zhang FR, Liu H, Irwanto A, Fu XA, Li Y, Yu GQ, Yu YX, Chen MF, Low HQ, Li JH, Bao FF, Foo JN, Bei JX, Jia XM, Liu J, Liany H, Wang N, Niu GY, Wang ZZ, Shi BQ, Tian HQ, Liu HX, Ma SS, Zhou Y, You JB, YangQ, Wang C, Chu TS, Liu DC, Yu XL, Sun YH, Ning Y, Wei ZH, Chen SL, Chen XC, Zhang ZX, Liu YX, Pulit SL, WuWB, Zheng ZY, Yang RD, Long H, Liu ZS, Wang JQ, Li M, Zhang LH, Wang H, Wang LM, Xiao P, Li JL, Huang ZM, Huang JX, Li Z, Liu J, Xiong L, Yang J, Wang XD, Yu DB, Lu XM, ZhouGZ, Yan LB, Shen JP, Zhang GC, Zeng YX, de Bakker PI, Chen SM, Liu JJ: HLA-B∗13:01 and the dapsone hypersensitivity syndrome. N Engl J Med 369: 1620-1628, 2013
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(2013)
N Engl J Med
, vol.369
, pp. 1620-1628
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Zhang, F.R.1
Liu, H.2
Irwanto, A.3
Fu, X.A.4
Li, Y.5
Yu, G.Q.6
Yu, Y.X.7
Chen, M.F.8
Low, H.Q.9
Li, J.H.10
Bao, F.F.11
Foo, J.N.12
Bei, J.X.13
Jia, X.M.14
Liu, J.15
Liany, H.16
Wang, N.17
Niu, G.Y.18
Wang, Z.Z.19
Shi, B.Q.20
Tian, H.Q.21
Liu, H.X.22
Brown, M.A.23
Zhou, Y.24
You, J.B.25
Yang, Q.26
Wang, C.27
Chu, T.S.28
Liu, D.C.29
Yu, X.L.30
Sun, Y.H.31
Ning, Y.32
Zh, W.33
Chen, S.L.34
Chen, X.C.35
Zhang, Z.X.36
Liu, Y.X.37
Pulit, S.L.38
Wu, W.B.39
Zheng, Z.Y.40
Yang, R.D.41
Long, H.42
Liu, Z.S.43
Wang, J.Q.44
Li, M.45
Zhang, L.H.46
Wang, H.47
Wang, L.M.48
Xiao, P.49
Li, J.L.50
Huang, Z.M.51
Huang, J.X.52
Li, Z.53
Liu, J.54
Xiong, L.55
Yang, J.56
Wang, X.D.57
Yu, D.B.58
Lu, X.M.59
Zhou, G.Z.60
Yan, L.B.61
Shen, J.P.62
Zhang, G.C.63
Zeng, Y.X.64
De Bakker, P.I.65
Chen, S.M.66
Liu, J.J.67
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