-
1
-
-
67749101270
-
Management of childhood onset nephrotic syndrome
-
Gipson DS, Massengill SF, Yao L, Nagaraj S, Smoyer WE, Mahan JD, Wigfall D, Miles P, Powell L, Lin JJ, Trachtman H, Greenbaum LA (2009) Management of childhood onset nephrotic syndrome. Pediatrics 124:747-757
-
(2009)
Pediatrics
, vol.124
, pp. 747-757
-
-
Gipson, D.S.1
Massengill, S.F.2
Yao, L.3
Nagaraj, S.4
Smoyer, W.E.5
Mahan, J.D.6
Wigfall, D.7
Miles, P.8
Powell, L.9
Lin, J.J.10
Trachtman, H.11
Greenbaum, L.A.12
-
2
-
-
33646127164
-
A case of unfulfilled expectations. Cytokines in idiopathic minimal lesion nephrotic syndrome
-
Araya CE, Wasserfall CH, Brusko TM, Mu W, Segal MS, Johnson RJ, Garin EH (2006) A case of unfulfilled expectations. Cytokines in idiopathic minimal lesion nephrotic syndrome. Pediatr Nephrol 21:603-610
-
(2006)
Pediatr Nephrol
, vol.21
, pp. 603-610
-
-
Araya, C.E.1
Wasserfall, C.H.2
Brusko, T.M.3
Mu, W.4
Segal, M.S.5
Johnson, R.J.6
Garin, E.H.7
-
3
-
-
54349098965
-
Urine proteomic profiling to identify biomarkers of steroid resistance in pediatric nephrotic syndrome
-
Traum AZ (2008) Urine proteomic profiling to identify biomarkers of steroid resistance in pediatric nephrotic syndrome. Expert Rev Proteomics 5:715-719
-
(2008)
Expert Rev Proteomics
, vol.5
, pp. 715-719
-
-
Traum, A.Z.1
-
4
-
-
77955012444
-
Hereditary nephrotic syndrome: A systematic approach for genetic testing and a review of associated podocyte gene mutations
-
Benoit G, Machuca E, Antignac C (2010) Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations. Pediatr Nephrol 25:1621-1632
-
(2010)
Pediatr Nephrol
, vol.25
, pp. 1621-1632
-
-
Benoit, G.1
Machuca, E.2
Antignac, C.3
-
5
-
-
79957817729
-
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome
-
Santin S, Bullich G, Tazon-Vega B, Garcia-Maset R, Gimenez I, Silva I, Ruiz P, Ballarin J, Torra R, Ars E (2011) Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol 6:1139-1148
-
(2011)
Clin J Am Soc Nephrol
, vol.6
, pp. 1139-1148
-
-
Santin, S.1
Bullich, G.2
Tazon-Vega, B.3
Garcia-Maset, R.4
Gimenez, I.5
Silva, I.6
Ruiz, P.7
Ballarin, J.8
Torra, R.9
Ars, E.10
-
6
-
-
77955646179
-
Association of trypanolytic apol1 variants with kidney disease in african americans
-
Genovese G, Friedman DJ, Ross MD, Lecordier L, Uzureau P, Freedman BI, Bowden DW, Langefeld CD, Oleksyk TK, Uscinski Knob AL, Bernhardy AJ, Hicks PJ, Nelson GW, Vanhollebeke B, Winkler CA, Kopp JB, Pays E, Pollak MR (2010) Association of trypanolytic ApoL1 variants with kidney disease in African Americans. Science 329:841-845
-
(2010)
Science
, vol.329
, pp. 841-845
-
-
Genovese, G.1
Friedman, D.J.2
Ross, M.D.3
Lecordier, L.4
Uzureau, P.5
Freedman, B.I.6
Bowden, D.W.7
Langefeld, C.D.8
Oleksyk, T.K.9
Uscinski Knob, A.L.10
Bernhardy, A.J.11
Hicks, P.J.12
Nelson, G.W.13
Vanhollebeke, B.14
Winkler, C.A.15
Kopp, J.B.16
Pays, E.17
Pollak, M.R.18
-
7
-
-
77956063973
-
Missense mutations in the apol1 gene are highly associated with end stage kidney disease risk previously attributed to the myh9 gene
-
Tzur S, Rosset S, Shemer R, Yudkovsky G, Selig S, Tarekegn A, Bekele E, Bradman N, Wasser WG, Behar DM, Skorecki K (2010) Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene. Hum Genet 128:345-350
-
(2010)
Hum Genet
, vol.128
, pp. 345-350
-
-
Tzur, S.1
Rosset, S.2
Shemer, R.3
Yudkovsky, G.4
Selig, S.5
Tarekegn, A.6
Bekele, E.7
Bradman, N.8
Wasser, W.G.9
Behar, D.M.10
Skorecki, K.11
-
8
-
-
79955465968
-
Common variation in gpc5 is associated with acquired nephrotic syndrome
-
Okamoto K, Tokunaga K, Doi K, Fujita T, Suzuki H, Katoh T, Watanabe T, Nishida N, Mabuchi A, Takahashi A, Kubo M, Maeda S, Nakamura Y, Noiri E (2011) Common variation in GPC5 is associated with acquired nephrotic syndrome. Nat Genet 43:459-463
-
(2011)
Nat Genet
, vol.43
, pp. 459-463
-
-
Okamoto, K.1
Tokunaga, K.2
Doi, K.3
Fujita, T.4
Suzuki, H.5
Katoh, T.6
Watanabe, T.7
Nishida, N.8
Mabuchi, A.9
Takahashi, A.10
Kubo, M.11
Maeda, S.12
Nakamura, Y.13
Noiri, E.14
-
9
-
-
79956225122
-
Ace i/d gene polymorphism can't predict the steroid responsiveness in asian children with idiopathic nephrotic syndrome: A metaanalysis
-
Zhou TB, Qin YH, Su LN, Lei FY, Huang WF, Zhao YJ (2011) ACE I/D gene polymorphism can't predict the steroid responsiveness in Asian children with idiopathic nephrotic syndrome: a metaanalysis. PLoS One 6:e19599
-
(2011)
PLoS One
, vol.6
-
-
Zhou, T.B.1
Qin, Y.H.2
Su, L.N.3
Lei, F.Y.4
Huang, W.F.5
Zhao, Y.J.6
-
10
-
-
80053370268
-
Genomewide association between glcci1 and response to glucocorticoid therapy in asthma
-
Tantisira KG, Lasky-Su J, Harada M, Murphy A, Litonjua AA, Himes BE, Lange C, Lazarus R, Sylvia J, Klanderman B, Duan QL, QiuW, Hirota T, Martinez FD, Mauger D, Sorkness C, Szefler S, Lazarus SC, Lemanske RF Jr., Peters SP, Lima JJ, Nakamura Y, Tamari M, Weiss ST (2011) Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma. N Engl J Med 365:1173-1183
-
(2011)
N Engl J Med
, vol.365
, pp. 1173-1183
-
-
Tantisira, K.G.1
Lasky-Su, J.2
Harada, M.3
Murphy, A.4
Litonjua, A.A.5
Himes, B.E.6
Lange, C.7
Lazarus, R.8
Sylvia, J.9
Klanderman, B.10
Duan, Q.L.11
QiuW Hirota, T.12
Martinez, F.D.13
Mauger, D.14
Sorkness, C.15
Szefler, S.16
Lazarus, S.C.17
Lemanske Jr., R.F.18
Peters, S.P.19
Lima, J.J.20
Nakamura, Y.21
Tamari, M.22
Weiss, S.T.23
more..
-
11
-
-
80555146723
-
Glcci1 deficiency leads to proteinuria
-
Nishibori Y, Katayama K, Parikka M, Oddsson A, Nukui M, Hultenby K,Wernerson A, He B, Ebarasi L, Raschperger E, Norlin J, Uhlen M, Patrakka J, Betsholtz C, Tryggvason K (2011) Glcci1 deficiency leads to proteinuria. J Am Soc Nephrol 22:2037-2046
-
(2011)
J Am Soc Nephrol
, vol.22
, pp. 2037-2046
-
-
Nishibori, Y.1
Katayama, K.2
Parikka, M.3
Oddsson, A.4
Nukui, M.5
Hultenby, K.6
Wernerson, A.7
He, B.8
Ebarasi, L.9
Raschperger, E.10
Norlin, J.11
Uhlen, M.12
Patrakka, J.13
Betsholtz, C.14
Tryggvason, K.15
-
12
-
-
83155175449
-
Polymorphisms of the mdr1 and mif genes in children with nephrotic syndrome
-
Choi HJ, Cho HY, Ro H, Lee SH, Han KH, Lee H, Kang HG, Ha IS, Choi Y, Cheong HI (2011) Polymorphisms of the MDR1 and MIF genes in children with nephrotic syndrome. Pediatr Nephrol 26:1981-1988
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 1981-1988
-
-
Choi, H.J.1
Cho, H.Y.2
Ro, H.3
Lee, S.H.4
Han, K.H.5
Lee, H.6
Kang, H.G.7
Ha, I.S.8
Choi, Y.9
Cheong, H.I.10
-
13
-
-
79959503826
-
The international hapmap project
-
Consortium IH (2003) The international HapMap project. Nature 426:789-796
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
Consortium, I.H.1
-
14
-
-
0028898022
-
Isolation of differentially expressed sequence tags from steroid-responsive cells using mrna differential display
-
Chapman MS, Qu N, Pascoe S, Chen WX, Apostol C, Gordon D, Miesfeld RL (1995) Isolation of differentially expressed sequence tags from steroid-responsive cells using mRNA differential display. Mol Cell Endocrinol 108:R1-R7
-
(1995)
Mol Cell Endocrinol
, vol.108
-
-
Chapman, M.S.1
Qu, N.2
Pascoe, S.3
Chen, W.X.4
Apostol, C.5
Gordon, D.6
Miesfeld, R.L.7
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