van de LogtAE, RijpmaSR, VinkCH, Prudon-RosmulderE, WetzelsJF, van BerkelM: The bias between different albumin assays may affect clinical decision-making. Kidney Int95: 1514–1517, 2019PubMed
van de LogtAE, RijpmaSR, VinkCH, Prudon-RosmulderE, WetzelsJF, van BerkelM: The bias between different albumin assays may affect clinical decision-making. Kidney Int 95: 1514–1517, 2019PubMed)| false
LagrueG, XheneumontS, BranellecA, HirbecG, WeilB: A vascular permeability factor elaborated from lymphocytes. I. Demonstration in patients with nephrotic syndrome. Biomedicine (Paris)23: 37–40, 1975PubMed
LagrueG, XheneumontS, BranellecA, HirbecG, WeilB: A vascular permeability factor elaborated from lymphocytes. I. Demonstration in patients with nephrotic syndrome. Biomedicine (Paris) 23: 37–40, 1975PubMed)| false
CheungPK, StulpB, ImmenschuhS, BorghuisT, BallerJF, BakkerWW: Is 100KF an isoform of hemopexin? Immunochemical characterization of the vasoactive plasma factor 100KF. J Am Soc Nephrol10: 1700–1708, 1999PubMed
CheungPK, StulpB, ImmenschuhS, BorghuisT, BallerJF, BakkerWW: Is 100KF an isoform of hemopexin? Immunochemical characterization of the vasoactive plasma factor 100KF. J Am Soc Nephrol 10: 1700–1708, 1999PubMed)| false
CheungPK, KlokPA, BallerJF, BakkerWW: Induction of experimental proteinuria in vivo following infusion of human plasma hemopexin. Kidney Int57: 1512–1520, 2000PubMed
CheungPK, KlokPA, BallerJF, BakkerWW: Induction of experimental proteinuria in vivo following infusion of human plasma hemopexin. Kidney Int 57: 1512–1520, 2000PubMed)| false
GarinEH, BlanchardDK, MatsushimaK, DjeuJY: IL-8 production by peripheral blood mononuclear cells in nephrotic patients. Kidney Int 45: 1311–1317, 1994PubMed)| false
KondoS, YoshizawaN, KusumiY, TakeuchiA, TorikataC: Studies of glomerular permeability factor (GPF) in focal segmental glomerular sclerosis and the relationship between GPF and vascular permeability factor (VPF). Clin Nephrol52: 278–284, 1999PubMed
KimAH, ChungJJ, AkileshS, KoziellA, JainS, HodginJB, et al.: B cell-derived IL-4 acts on podocytes to induce proteinuria and foot process effacement. JCI Insight2: e81836, 2017PubMed
YoshikawaN, NakanishiK, SakoM, ObaMS, MoriR, OtaE, et al.; Japanese Study Group of Kidney Disease in Children: A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment. Kidney Int87: 225–232, 2015PubMed
YoshikawaN, NakanishiK, SakoM, ObaMS, MoriR, OtaE, ; Japanese Study Group of Kidney Disease in Children: A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment. Kidney Int 87: 225–232, 2015PubMed)| false
SinhaA, SahaA, KumarM, SharmaS, AfzalK, MehtaA, et al.: Extending initial prednisolone treatment in a randomized control trial from 3 to 6 months did not significantly influence the course of illness in children with steroid-sensitive nephrotic syndrome. Kidney Int87: 217–224, 2015PubMed
SinhaA, SahaA, KumarM, SharmaS, AfzalK, MehtaA, : Extending initial prednisolone treatment in a randomized control trial from 3 to 6 months did not significantly influence the course of illness in children with steroid-sensitive nephrotic syndrome. Kidney Int 87: 217–224, 2015PubMed)| false
WebbNJA, WoolleyRL, LambeT, FrewE, BrettellEA, BarsoumEN, et al.; PREDNOS Collaborative Group: Long term tapering versus standard prednisolone treatment for first episode of childhood nephrotic syndrome: Phase III randomised controlled trial and economic evaluation. BMJ365: l1800, 2019PubMed
WebbNJA, WoolleyRL, LambeT, FrewE, BrettellEA, BarsoumEN, ; PREDNOS Collaborative Group: Long term tapering versus standard prednisolone treatment for first episode of childhood nephrotic syndrome: Phase III randomised controlled trial and economic evaluation. BMJ 365: l1800, 2019PubMed)| false
MeyrierA, CondaminMC, BroneerD; Collaborative Group of the French Society of Nephrology: Treatment of adult idiopathic nephrotic syndrome with cyclosporin A: Minimal-change disease and focal-segmental glomerulosclerosis. Clin Nephrol35[Suppl 1]: S37–S42, 1991PubMed
MeyrierA, CondaminMC, BroneerD; Collaborative Group of the French Society of Nephrology: Treatment of adult idiopathic nephrotic syndrome with cyclosporin A: Minimal-change disease and focal-segmental glomerulosclerosis. Clin Nephrol 35[Suppl 1]: S37–S42, 1991PubMed)| false
Medjeral-ThomasNR, LawrenceC, CondonM, SoodB, WarwickerP, BrownH, et al.: Randomized, controlled trial of tacrolimus and prednisolone monotherapy for adults with de novo minimal change disease: A multicenter, randomized, controlled trial. Clin J Am Soc Nephrol15: 209–218, 2020PubMed
Medjeral-ThomasNR, LawrenceC, CondonM, SoodB, WarwickerP, BrownH, : Randomized, controlled trial of tacrolimus and prednisolone monotherapy for adults with de novo minimal change disease: A multicenter, randomized, controlled trial. Clin J Am Soc Nephrol 15: 209–218, 2020PubMed)| false
GellermannJ, WeberL, PapeL, TönshoffB, HoyerP, QuerfeldU; Gesellschaft für Pädiatrische Nephrologie (GPN): Mycophenolate mofetil versus cyclosporin A in children with frequently relapsing nephrotic syndrome. J Am Soc Nephrol24: 1689–1697, 2013PubMed
GellermannJ, WeberL, PapeL, TönshoffB, HoyerP, QuerfeldU; Gesellschaft für Pädiatrische Nephrologie (GPN): Mycophenolate mofetil versus cyclosporin A in children with frequently relapsing nephrotic syndrome. J Am Soc Nephrol 24: 1689–1697, 2013PubMed)| false
GengHY, JiLN, ChenCY, TuJ, LiHR, BaoR, et al.: [Mycophenolate mofetil versus cyclosporine A in children with primary refractory nephrotic syndrome]. Zhonghua Er Ke Za Zhi56: 651–656, 2018PubMed
GengHY, JiLN, ChenCY, TuJ, LiHR, BaoR, : [Mycophenolate mofetil versus cyclosporine A in children with primary refractory nephrotic syndrome]. Zhonghua Er Ke Za Zhi 56: 651–656, 2018PubMed)| false
SinhaA, PuraswaniM, KalaivaniM, GoyalP, HariP, BaggaA: Efficacy and safety of mycophenolate mofetil versus levamisole in frequently relapsing nephrotic syndrome: An open-label randomized controlled trial. Kidney Int 95: 210–218, 2019PubMed)| false
RémyP, AudardV, NatellaPA, PelleG, DussolB, Leray-MoraguesH, et al.; MSN Trial Investigators: An open-label randomized controlled trial of low-dose corticosteroid plus enteric-coated mycophenolate sodium versus standard corticosteroid treatment for minimal change nephrotic syndrome in adults (MSN study). Kidney Int94: 1217–1226, 2018PubMed
BenzK, DötschJ, RascherW, StachelD: Change of the course of steroid-dependent nephrotic syndrome after rituximab therapy. Pediatr Nephrol19: 794–797, 2004PubMed
RavaniP, RossiR, BonanniA, QuinnRR, SicaF, BodriaM, et al.: Rituximab in children with steroid-dependent nephrotic syndrome: A multicenter, open-label, noninferiority, randomized controlled trial. J Am Soc Nephrol26: 2259–2266, 2015PubMed
RuggenentiP, RuggieroB, CravediP, VivarelliM, MassellaL, MarasàM, et al.; Rituximab in Nephrotic Syndrome of Steroid-Dependent or Frequently Relapsing Minimal Change Disease Or Focal Segmental Glomerulosclerosis (NEMO) Study Group: Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome. J Am Soc Nephrol25: 850–863, 2014PubMed
HoganJ, DossierC, KwonT, MacherMA, MaisinA, CoudercA, et al.: Effect of different rituximab regimens on B cell depletion and time to relapse in children with steroid-dependent nephrotic syndrome. Pediatr Nephrol34: 253–259, 2019PubMed
HoganJ, DossierC, KwonT, MacherMA, MaisinA, CoudercA, : Effect of different rituximab regimens on B cell depletion and time to relapse in children with steroid-dependent nephrotic syndrome. Pediatr Nephrol 34: 253–259, 2019PubMed)| false
ChanEY, WebbH, YuE, GhiggeriGM, KemperMJ, MaAL, et al.: Both the rituximab dose and maintenance immunosuppression in steroid-dependent/frequently-relapsing nephrotic syndrome have important effects on outcomes. Kidney Int97: 393–401, 2020PubMed
ChanEY, WebbH, YuE, GhiggeriGM, KemperMJ, MaAL, : Both the rituximab dose and maintenance immunosuppression in steroid-dependent/frequently-relapsing nephrotic syndrome have important effects on outcomes. Kidney Int 97: 393–401, 2020PubMed)| false
RavaniP, MagnascoA, EdefontiA, MurerL, RossiR, GhioL, et al.: Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: A randomized controlled trial. Clin J Am Soc Nephrol6: 1308–1315, 2011PubMed
RavaniP, MagnascoA, EdefontiA, MurerL, RossiR, GhioL, : Short-term effects of rituximab in children with steroid- and calcineurin-dependent nephrotic syndrome: A randomized controlled trial. Clin J Am Soc Nephrol 6: 1308–1315, 2011PubMed)| false
RavaniP, PonticelliA, SicilianoC, FornoniA, MagnascoA, SicaF, et al.: Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome. Kidney Int84: 1025–1033, 2013PubMed
RavaniP, PonticelliA, SicilianoC, FornoniA, MagnascoA, SicaF, : Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor-dependent idiopathic nephrotic syndrome. Kidney Int 84: 1025–1033, 2013PubMed)| false
MagnascoA, RavaniP, EdefontiA, MurerL, GhioL, BelingheriM, et al.: Rituximab in children with resistant idiopathic nephrotic syndrome. J Am Soc Nephrol23: 1117–1124, 2012PubMed
RavaniP, BonanniA, GhiggeriGM: Randomised controlled trial comparing ofatumumab to rituximab in children with steroid-dependent and calcineurin inhibitor-dependent idiopathic nephrotic syndrome: Study protocol. BMJ Open7: e013319, 2017PubMed
RavaniP, BonanniA, GhiggeriGM: Randomised controlled trial comparing ofatumumab to rituximab in children with steroid-dependent and calcineurin inhibitor-dependent idiopathic nephrotic syndrome: Study protocol. BMJ Open 7: e013319, 2017PubMed)| false
IwabuchiY, MiyabeY, MakabeS, NakanoM, ManabeS, KarasawaK, et al.: Comparison of the response of frequently relapsing steroid-dependent minimal change nephrotic syndrome to rituximab therapy between childhood-onset and adult-onset disease. Medicine (Baltimore)97: e12704, 2018PubMed
IwabuchiY, MiyabeY, MakabeS, NakanoM, ManabeS, KarasawaK, : Comparison of the response of frequently relapsing steroid-dependent minimal change nephrotic syndrome to rituximab therapy between childhood-onset and adult-onset disease. Medicine (Baltimore) 97: e12704, 2018PubMed)| false
FenoglioR, SciasciaS, BeltrameG, MesianoP, FerroM, QuattrocchioG, et al.: Rituximab as a front-line therapy for adult-onset minimal change disease with nephrotic syndrome. Oncotarget9: 28799–28804, 2018PubMed
KittanamongkolchaiW, CheungpasitpornW, ZandL: Efficacy and safety of adrenocorticotropic hormone treatment in glomerular diseases: A systematic review and meta-analysis. Clin Kidney J9: 387–396, 2016PubMed
KittanamongkolchaiW, CheungpasitpornW, ZandL: Efficacy and safety of adrenocorticotropic hormone treatment in glomerular diseases: A systematic review and meta-analysis. Clin Kidney J 9: 387–396, 2016PubMed)| false
MadanA, Mijovic-DasS, StankovicA, TeehanG, MilwardAS, KhastgirA: Acthar gel in the treatment of nephrotic syndrome: A multicenter retrospective case series. BMC Nephrol17: 37, 2016PubMed
MadanA, Mijovic-DasS, StankovicA, TeehanG, MilwardAS, KhastgirA: Acthar gel in the treatment of nephrotic syndrome: A multicenter retrospective case series. BMC Nephrol 17: 37, 2016PubMed)| false
SzetoCC, LaiFM, ChowKM, KwanBC, KwongVW, LeungCB, et al.: Long-term outcome of biopsy-proven minimal change nephropathy in Chinese adults. Am J Kidney Dis65: 710–718, 2015PubMed
SethiS, GlassockRJ, FervenzaFC: Focal segmental glomerulosclerosis: Towards a better understanding for the practicing nephrologist. Nephrol Dial Transplant30: 375–384, 2015PubMed
KrizW, LemleyKV: A potential role for mechanical forces in the detachment of podocytes and the progression of CKD. J Am Soc Nephrol26: 258–269, 2015PubMed
KrizW, LemleyKV: A potential role for mechanical forces in the detachment of podocytes and the progression of CKD. J Am Soc Nephrol 26: 258–269, 2015PubMed)| false
RovinBH, AdlerSG, BarrattJ, BridouxF, BurdgeKA, ChanTM, et al.: Executive summary of the KDIGO 2021 guideline for the management of glomerular diseases. Kidney Int100: 753–779, 2021PubMed
RovinBH, AdlerSG, BarrattJ, BridouxF, BurdgeKA, ChanTM, : Executive summary of the KDIGO 2021 guideline for the management of glomerular diseases. Kidney Int 100: 753–779, 2021PubMed)| false
SchwartzmanM, ReginensiA, WongJS, BasgenJM, MeliambroK, NicholasSB, et al.: Podocyte-specific deletion of Yes-associated protein causes FSGS and progressive renal failure. J Am Soc Nephrol27: 216–226, 2016PubMed
SavinVJ, SharmaM, ZhouJ, GennochiD, FieldsT, SharmaR, et al.: Renal and hematological effects of CLCF-1, a B-cell-stimulating cytokine of the IL-6 family. J Immunol Res2015: 714964, 2015PubMed
SavinVJ, SharmaM, ZhouJ, GennochiD, FieldsT, SharmaR, : Renal and hematological effects of CLCF-1, a B-cell-stimulating cytokine of the IL-6 family. J Immunol Res 2015: 714964, 2015PubMed)| false
WeiC, El HindiS, LiJ, FornoniA, GoesN, SageshimaJ, et al.: Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis. Nat Med17: 952–960, 2011PubMed
WeiC, El HindiS, LiJ, FornoniA, GoesN, SageshimaJ, : Circulating urokinase receptor as a cause of focal segmental glomerulosclerosis. Nat Med 17: 952–960, 2011PubMed)| false
De VrieseAS, SethiS, NathKA, GlassockRJ, FervenzaFC: Differentiating primary, genetic, and secondary FSGS in adults: A clinicopathologic approach. J Am Soc Nephrol29: 759–774, 2018PubMed
De VrieseAS, SethiS, NathKA, GlassockRJ, FervenzaFC: Differentiating primary, genetic, and secondary FSGS in adults: A clinicopathologic approach. J Am Soc Nephrol 29: 759–774, 2018PubMed)| false
PerkovicV, JardineMJ, NealB, BompointS, HeerspinkHJL, CharytanDM, et al.; CREDENCE Trial Investigators: Canagliflozin and renal outcomes in type 2 diabetes and nephropathy. N Engl J Med380: 2295–2306, 2019PubMed
PerkovicV, JardineMJ, NealB, BompointS, HeerspinkHJL, CharytanDM, ; CREDENCE Trial Investigators: Canagliflozin and renal outcomes in type 2 diabetes and nephropathy. N Engl J Med 380: 2295–2306, 2019PubMed)| false
van den BergJG, van den Bergh WeermanMA, AssmannKJ, WeeningJJ, FlorquinS: Podocyte foot process effacement is not correlated with the level of proteinuria in human glomerulopathies. Kidney Int66: 1901–1906, 2004PubMed
van den BergJG, van den Bergh WeermanMA, AssmannKJ, WeeningJJ, FlorquinS: Podocyte foot process effacement is not correlated with the level of proteinuria in human glomerulopathies. Kidney Int 66: 1901–1906, 2004PubMed)| false
DeegensJK, DijkmanHB, BormGF, SteenbergenEJ, van den BergJG, WeeningJJ, et al.: Podocyte foot process effacement as a diagnostic tool in focal segmental glomerulosclerosis. Kidney Int74: 1568–1576, 2008PubMed
DeegensJK, DijkmanHB, BormGF, SteenbergenEJ, van den BergJG, WeeningJJ, : Podocyte foot process effacement as a diagnostic tool in focal segmental glomerulosclerosis. Kidney Int 74: 1568–1576, 2008PubMed)| false
HommosMS, De VrieseAS, AlexanderMP, SethiS, VaughanL, ZandL, et al.: The incidence of primary vs secondary focal segmental glomerulosclerosis: A clinicopathologic study. Mayo Clin Proc92: 1772–1781, 2017PubMed
HommosMS, De VrieseAS, AlexanderMP, SethiS, VaughanL, ZandL, : The incidence of primary vs secondary focal segmental glomerulosclerosis: A clinicopathologic study. Mayo Clin Proc 92: 1772–1781, 2017PubMed)| false
ZandL, GlassockRJ, De VrieseAS, SethiS, FervenzaFC: What are we missing in the clinical trials of focal segmental glomerulosclerosis?Nephrol Dial Transplant32[Suppl 1]: i14–i21, 2017PubMed
ZandL, GlassockRJ, De VrieseAS, SethiS, FervenzaFC: What are we missing in the clinical trials of focal segmental glomerulosclerosis? Nephrol Dial Transplant 32[Suppl 1]: i14–i21, 2017PubMed)| false
RoodIM, BavinckA, Lipska-ZiętkiewiczBS, LugtenbergD, SchaeferF, DeegensJKJ, et al.: Later response to corticosteroids in adults with primary focal segmental glomerular sclerosis is associated with favorable outcomes. Kidney Int Rep7: 87–98, 2021PubMed
RoodIM, BavinckA, Lipska-ZiętkiewiczBS, LugtenbergD, SchaeferF, DeegensJKJ, : Later response to corticosteroids in adults with primary focal segmental glomerular sclerosis is associated with favorable outcomes. Kidney Int Rep 7: 87–98, 2021PubMed)| false
CattranDC, AppelGB, HebertLA, HunsickerLG, PohlMA, HoyWE, et al.; North America Nephrotic Syndrome Study Group: A randomized trial of cyclosporine in patients with steroid-resistant focal segmental glomerulosclerosis. Kidney Int56: 2220–2226, 1999PubMed
CattranDC, AppelGB, HebertLA, HunsickerLG, PohlMA, HoyWE, ; North America Nephrotic Syndrome Study Group: A randomized trial of cyclosporine in patients with steroid-resistant focal segmental glomerulosclerosis. Kidney Int 56: 2220–2226, 1999PubMed)| false
LaurinLP, GasimAM, PoultonCJ, HoganSL, JennetteJC, FalkRJ, et al.: Treatment with glucocorticoids or calcineurin inhibitors in primary FSGS. Clin J Am Soc Nephrol11: 386–394, 2016PubMed
FaulC, DonnellyM, Merscher-GomezS, ChangYH, FranzS, DelfgaauwJ, et al.: The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A. Nat Med14: 931–938, 2008PubMed
FaulC, DonnellyM, Merscher-GomezS, ChangYH, FranzS, DelfgaauwJ, : The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A. Nat Med 14: 931–938, 2008PubMed)| false
MeyrierA, NoëlLH, AuricheP, CallardP; Collaborative Group of the Société de Néphrologie: Long-term renal tolerance of cyclosporin A treatment in adult idiopathic nephrotic syndrome. Kidney Int45: 1446–1456, 1994PubMed
MeyrierA, NoëlLH, AuricheP, CallardP; Collaborative Group of the Société de Néphrologie: Long-term renal tolerance of cyclosporin A treatment in adult idiopathic nephrotic syndrome. Kidney Int 45: 1446–1456, 1994PubMed)| false
DaSilvaI, HuertaA, QuintanaL, RedondoB, IglesiasE, DraibeJ, et al.; Spanish Group for the Study of Glomerular Diseases (GLOSEN): Rituximab for steroid-dependent or frequently relapsing idiopathic nephrotic syndrome in adults: A retrospective, multicenter study in Spain. BioDrugs31: 239–249, 2017PubMed
DaSilvaI, HuertaA, QuintanaL, RedondoB, IglesiasE, DraibeJ, ; Spanish Group for the Study of Glomerular Diseases (GLOSEN): Rituximab for steroid-dependent or frequently relapsing idiopathic nephrotic syndrome in adults: A retrospective, multicenter study in Spain. BioDrugs 31: 239–249, 2017PubMed)| false
TedescoM, MesciaF, PisaniI, AllinoviM, CasazzaG, Del VecchioL, et al.; Italian Society of Nephrology Immunopathology Working Group: The role of rituximab in primary focal segmental glomerular sclerosis of the adult. Kidney Int Rep7: 1878–1886, 2022PubMed
TedescoM, MesciaF, PisaniI, AllinoviM, CasazzaG, Del VecchioL, ; Italian Society of Nephrology Immunopathology Working Group: The role of rituximab in primary focal segmental glomerular sclerosis of the adult. Kidney Int Rep 7: 1878–1886, 2022PubMed)| false
FurieRA, ArocaG, CascinoMD, GargJP, RovinBH, AlvarezA, et al.: B-cell depletion with obinutuzumab for the treatment of proliferative lupus nephritis: A randomised, double-blind, placebo-controlled trial. Ann Rheum Dis81: 100–107, 2022PubMed
FurieRA, ArocaG, CascinoMD, GargJP, RovinBH, AlvarezA, : B-cell depletion with obinutuzumab for the treatment of proliferative lupus nephritis: A randomised, double-blind, placebo-controlled trial. Ann Rheum Dis 81: 100–107, 2022PubMed)| false
KlomjitN, FervenzaFC, ZandL: Successful treatment of patients with refractory PLA2R-associated membranous nephropathy with obinutuzumab: A report of 3 cases. Am J Kidney Dis76: 883–888, 2020PubMed
KlomjitN, FervenzaFC, ZandL: Successful treatment of patients with refractory PLA2R-associated membranous nephropathy with obinutuzumab: A report of 3 cases. Am J Kidney Dis 76: 883–888, 2020PubMed)| false
GipsonDS, TrachtmanH, KaskelFJ, GreeneTH, RadevaMK, GassmanJJ, et al.: Clinical trial of focal segmental glomerulosclerosis in children and young adults. Kidney Int80: 868–878, 2011PubMed
GipsonDS, TrachtmanH, KaskelFJ, GreeneTH, RadevaMK, GassmanJJ, : Clinical trial of focal segmental glomerulosclerosis in children and young adults. Kidney Int 80: 868–878, 2011PubMed)| false
TrachtmanH, NelsonP, AdlerS, CampbellKN, ChaudhuriA, DerebailVK, et al.; DUET Study Group: DUET: A phase 2 study evaluating the efficacy and safety of sparsentan in patients with FSGS. J Am Soc Nephrol29: 2745–2754, 2018PubMed
TrachtmanH, NelsonP, AdlerS, CampbellKN, ChaudhuriA, DerebailVK, ; DUET Study Group: DUET: A phase 2 study evaluating the efficacy and safety of sparsentan in patients with FSGS. J Am Soc Nephrol 29: 2745–2754, 2018PubMed)| false
WheelerDC, JongsN, StefanssonBV, ChertowGM, GreeneT, HouFF, et al.; DAPA-CKD Trial Committees and Investigators: Safety and efficacy of dapagliflozin in patients with focal segmental glomerulosclerosis: A prespecified analysis of the dapagliflozin and prevention of adverse outcomes in chronic kidney disease (DAPA-CKD) trial. Nephrol Dial Transplant37: 1647–1656, 2022PubMed
WheelerDC, JongsN, StefanssonBV, ChertowGM, GreeneT, HouFF, ; DAPA-CKD Trial Committees and Investigators: Safety and efficacy of dapagliflozin in patients with focal segmental glomerulosclerosis: A prespecified analysis of the dapagliflozin and prevention of adverse outcomes in chronic kidney disease (DAPA-CKD) trial. Nephrol Dial Transplant 37: 1647–1656, 2022PubMed)| false
SantínS, BullichG, Tazón-VegaB, García-MasetR, GiménezI, SilvaI, et al.: Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol6: 1139–1148, 2011PubMed
SantínS, BullichG, Tazón-VegaB, García-MasetR, GiménezI, SilvaI, : Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol 6: 1139–1148, 2011PubMed)| false
MiaoJ, Pinto E VairoF, HoganMC, EricksonSB, El TersM, BentallAJ, et al.: Identification of genetic causes of focal segmental glomerulosclerosis increases with proper patient selection. Mayo Clin Proc96: 2342–2353, 2021PubMed
MiaoJ, Pinto E VairoF, HoganMC, EricksonSB, El TersM, BentallAJ, : Identification of genetic causes of focal segmental glomerulosclerosis increases with proper patient selection. Mayo Clin Proc 96: 2342–2353, 2021PubMed)| false
YaoT, UdwanK, JohnR, RanaA, HaghighiA, XuL, et al.: Integration of genetic testing and pathology for the diagnosis of adults with FSGS. Clin J Am Soc Nephrol14: 213–223, 2019PubMed
YaoT, UdwanK, JohnR, RanaA, HaghighiA, XuL, : Integration of genetic testing and pathology for the diagnosis of adults with FSGS. Clin J Am Soc Nephrol 14: 213–223, 2019PubMed)| false
BüscherAK, BeckBB, MelkA, HoefeleJ, KranzB, BamborschkeD, et al.; German Pediatric Nephrology Association (GPN): Rapid response to cyclosporin A and favorable renal outcome in nongenetic versus genetic steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol11: 245–253, 2016PubMed
BüscherAK, BeckBB, MelkA, HoefeleJ, KranzB, BamborschkeD, ; German Pediatric Nephrology Association (GPN): Rapid response to cyclosporin A and favorable renal outcome in nongenetic versus genetic steroid-resistant nephrotic syndrome. Clin J Am Soc Nephrol 11: 245–253, 2016PubMed)| false
BobartSA, TehranianS, SethiS, AlexanderMP, NasrSH, Moura MartaC, et al.: A target antigen-based approach to the classification of membranous nephropathy. Mayo Clin Proc96: 577–591, 2021PubMed
BobartSA, TehranianS, SethiS, AlexanderMP, NasrSH, Moura MartaC, : A target antigen-based approach to the classification of membranous nephropathy. Mayo Clin Proc 96: 577–591, 2021PubMed)| false
SethiS, DebiecH, MaddenB, VivarelliM, CharlesworthMC, RavindranA, et al.: Semaphorin 3B-associated membranous nephropathy is a distinct type of disease predominantly present in pediatric patients. Kidney Int98: 1253–1264, 2020PubMed
SethiS, DebiecH, MaddenB, VivarelliM, CharlesworthMC, RavindranA, : Semaphorin 3B-associated membranous nephropathy is a distinct type of disease predominantly present in pediatric patients. Kidney Int 98: 1253–1264, 2020PubMed)| false
BobartSA, HanH, TehranianS, De VrieseAS, RomanJCL, SethiS, et al.: Noninvasive diagnosis of PLA2R-associated membranous nephropathy: A validation study. Clin J Am Soc Nephrol16: 1833–1839, 2021PubMed
BehnertA, SchifferM, Müller-DeileJ, BeckLHJr, MahlerM, FritzlerMJ: Antiphospholipase A2 receptor autoantibodies: A comparison of three different immunoassays for the diagnosis of idiopathic membranous nephropathy. J Immunol Res2014: 143274, 2014PubMed
BehnertA, SchifferM, Müller-DeileJ, BeckLHJr, MahlerM, FritzlerMJ: Antiphospholipase A2 receptor autoantibodies: A comparison of three different immunoassays for the diagnosis of idiopathic membranous nephropathy. J Immunol Res 2014: 143274, 2014PubMed)| false
TimmermansSA, Abdul HamidMA, Cohen TervaertJW, DamoiseauxJG, van PaassenP; Limburg Renal Registry: Anti-PLA2R antibodies as a prognostic factor in PLA2R-related membranous nephropathy. Am J Nephrol42: 70–77, 2015PubMed
TimmermansSA, Abdul HamidMA, Cohen TervaertJW, DamoiseauxJG, van PaassenP; Limburg Renal Registry: Anti-PLA2R antibodies as a prognostic factor in PLA2R-related membranous nephropathy. Am J Nephrol 42: 70–77, 2015PubMed)| false
HoxhaE, HarendzaS, PinnschmidtH, PanzerU, StahlRA: PLA2R antibody levels and clinical outcome in patients with membranous nephropathy and non-nephrotic range proteinuria under treatment with inhibitors of the renin-angiotensin system. PLoS One9: e110681, 2014PubMed
HoxhaE, HarendzaS, PinnschmidtH, PanzerU, StahlRA: PLA2R antibody levels and clinical outcome in patients with membranous nephropathy and non-nephrotic range proteinuria under treatment with inhibitors of the renin-angiotensin system. PLoS One 9: e110681, 2014PubMed)| false
KanigicherlaD, GummadovaJ, McKenzieEA, RobertsSA, HarrisS, NikamM, et al.: Anti-PLA2R antibodies measured by ELISA predict long-term outcome in a prevalent population of patients with idiopathic membranous nephropathy. Kidney Int83: 940–948, 2013PubMed
KanigicherlaD, GummadovaJ, McKenzieEA, RobertsSA, HarrisS, NikamM, : Anti-PLA2R antibodies measured by ELISA predict long-term outcome in a prevalent population of patients with idiopathic membranous nephropathy. Kidney Int 83: 940–948, 2013PubMed)| false
BurbeloPD, JoshiM, ChaturvediA, LittleDJ, ThurlowJS, WaldmanM, et al.: Detection of PLA2R autoantibodies before the diagnosis of membranous nephropathy. J Am Soc Nephrol31: 208–217, 2020PubMed
BurbeloPD, JoshiM, ChaturvediA, LittleDJ, ThurlowJS, WaldmanM, : Detection of PLA2R autoantibodies before the diagnosis of membranous nephropathy. J Am Soc Nephrol 31: 208–217, 2020PubMed)| false
Seitz-PolskiB, DollaG, PayréC, GirardCA, PolidoriJ, ZorziK, et al.: Epitope spreading of autoantibody response to PLA2R associates with poor prognosis in membranous nephropathy. J Am Soc Nephrol27: 1517–1533, 2016PubMed
MedranoAS, EscalanteEJ, CáceresCC, PamplonaIA, AllendeMT, TerradesNR, et al.: Prognostic value of the dynamics of M-type phospholipase A2 receptor antibody titers in patients with idiopathic membranous nephropathy treated with two different immunosuppression regimens. Biomarkers20: 77–83, 2015PubMed
MedranoAS, EscalanteEJ, CáceresCC, PamplonaIA, AllendeMT, TerradesNR, : Prognostic value of the dynamics of M-type phospholipase A2 receptor antibody titers in patients with idiopathic membranous nephropathy treated with two different immunosuppression regimens. Biomarkers 20: 77–83, 2015PubMed)| false
De VrieseAS, GlassockRJ, NathKA, SethiS, FervenzaFC: A proposal for a serology-based approach to membranous nephropathy. J Am Soc Nephrol28: 421–430, 2017PubMed
De VrieseAS, GlassockRJ, NathKA, SethiS, FervenzaFC: A proposal for a serology-based approach to membranous nephropathy. J Am Soc Nephrol 28: 421–430, 2017PubMed)| false
RenS, WuC, ZhangY, WangAY, LiG, WangL, et al.: An update on clinical significance of use of THSD7A in diagnosing idiopathic membranous nephropathy: A systematic review and meta-analysis of THSD7A in IMN. Ren Fail40: 306–313, 2018PubMed
RenS, WuC, ZhangY, WangAY, LiG, WangL, : An update on clinical significance of use of THSD7A in diagnosing idiopathic membranous nephropathy: A systematic review and meta-analysis of THSD7A in IMN. Ren Fail 40: 306–313, 2018PubMed)| false
HoxhaE, BeckLHJr, WiechT, TomasNM, ProbstC, MindorfS, et al.: An indirect immunofluorescence method facilitates detection of thrombospondin type 1 domain-containing 7A-specific antibodies in membranous nephropathy. J Am Soc Nephrol28: 520–531, 2017PubMed
RavindranA, Casal MouraM, FervenzaFC, NasrSH, AlexanderMP, FidlerME, et al.: In patients with membranous lupus nephritis, exostosin-positivity and exostosin-negativity represent two different phenotypes. J Am Soc Nephrol32: 695–706, 2021PubMed
RavindranA, Casal MouraM, FervenzaFC, NasrSH, AlexanderMP, FidlerME, : In patients with membranous lupus nephritis, exostosin-positivity and exostosin-negativity represent two different phenotypes. J Am Soc Nephrol 32: 695–706, 2021PubMed)| false
WangC, LiuY, ZhangM, YangF, XuF, ShiS, et al.: Glomerular exostosin as a subtype and activity marker of class 5 lupus nephritis. Clin J Am Soc Nephrol17: 986–993, 2022PubMed
WangC, LiuY, ZhangM, YangF, XuF, ShiS, : Glomerular exostosin as a subtype and activity marker of class 5 lupus nephritis. Clin J Am Soc Nephrol 17: 986–993, 2022PubMed)| false
JhaV, GanguliA, SahaTK, KohliHS, SudK, GuptaKL, et al.: A randomized, controlled trial of steroids and cyclophosphamide in adults with nephrotic syndrome caused by idiopathic membranous nephropathy. J Am Soc Nephrol18: 1899–1904, 2007PubMed
JhaV, GanguliA, SahaTK, KohliHS, SudK, GuptaKL, : A randomized, controlled trial of steroids and cyclophosphamide in adults with nephrotic syndrome caused by idiopathic membranous nephropathy. J Am Soc Nephrol 18: 1899–1904, 2007PubMed)| false
PonticelliC, ZucchelliP, PasseriniP, CesanaB, LocatelliF, PasqualiS, et al.: A 10-year follow-up of a randomized study with methylprednisolone and chlorambucil in membranous nephropathy. Kidney Int48: 1600–1604, 1995PubMed
PonticelliC, ZucchelliP, PasseriniP, CesanaB, LocatelliF, PasqualiS, : A 10-year follow-up of a randomized study with methylprednisolone and chlorambucil in membranous nephropathy. Kidney Int 48: 1600–1604, 1995PubMed)| false
CattranDC, GreenwoodC, RitchieS, BernsteinK, ChurchillDN, ClarkWF, et al.; Canadian Glomerulonephritis Study Group: A controlled trial of cyclosporine in patients with progressive membranous nephropathy. Kidney Int47: 1130–1135, 1995PubMed
CattranDC, GreenwoodC, RitchieS, BernsteinK, ChurchillDN, ClarkWF, ; Canadian Glomerulonephritis Study Group: A controlled trial of cyclosporine in patients with progressive membranous nephropathy. Kidney Int 47: 1130–1135, 1995PubMed)| false
CattranDC, AppelGB, HebertLA, HunsickerLG, PohlMA, HoyWE, et al.; North America Nephrotic Syndrome Study Group: Cyclosporine in patients with steroid-resistant membranous nephropathy: A randomized trial. Kidney Int59: 1484–1490, 2001PubMed
CattranDC, AppelGB, HebertLA, HunsickerLG, PohlMA, HoyWE, ; North America Nephrotic Syndrome Study Group: Cyclosporine in patients with steroid-resistant membranous nephropathy: A randomized trial. Kidney Int 59: 1484–1490, 2001PubMed)| false
AlexopoulosE, PapagianniA, TsamelashviliM, LeontsiniM, MemmosD: Induction and long-term treatment with cyclosporine in membranous nephropathy with the nephrotic syndrome. Nephrol Dial Transplant21: 3127–3132, 2006PubMed
AlexopoulosE, PapagianniA, TsamelashviliM, LeontsiniM, MemmosD: Induction and long-term treatment with cyclosporine in membranous nephropathy with the nephrotic syndrome. Nephrol Dial Transplant 21: 3127–3132, 2006PubMed)| false
PragaM, BarrioV, JuárezGF, LuñoJ; Grupo Español de Estudio de la Nefropatía Membranosa: Tacrolimus monotherapy in membranous nephropathy: A randomized controlled trial. Kidney Int71: 924–930, 2007PubMed
PragaM, BarrioV, JuárezGF, LuñoJ; Grupo Español de Estudio de la Nefropatía Membranosa: Tacrolimus monotherapy in membranous nephropathy: A randomized controlled trial. Kidney Int 71: 924–930, 2007PubMed)| false
RamachandranR, HnHK, KumarV, NadaR, YadavAK, GoyalA, et al.: Tacrolimus combined with corticosteroids versus modified Ponticelli regimen in treatment of idiopathic membranous nephropathy: Randomized control trial. Nephrology (Carlton)21: 139–146, 2016PubMed
CaroJ, Gutiérrez-SolísE, Rojas-RiveraJ, AgrazI, RamosN, RabascoC, et al.; Grupo de Estudio de las Enfermedades Glomerulares de la Sociedad Española de Nefrología (GLOSEN): Predictors of response and relapse in patients with idiopathic membranous nephropathy treated with tacrolimus. Nephrol Dial Transplant30: 467–474, 2015PubMed
CaroJ, Gutiérrez-SolísE, Rojas-RiveraJ, AgrazI, RamosN, RabascoC, ; Grupo de Estudio de las Enfermedades Glomerulares de la Sociedad Española de Nefrología (GLOSEN): Predictors of response and relapse in patients with idiopathic membranous nephropathy treated with tacrolimus. Nephrol Dial Transplant 30: 467–474, 2015PubMed)| false
DahanK, DebiecH, PlaisierE, CachanadoM, RousseauA, WakselmanL, et al.; GEMRITUX Study Group: Rituximab for severe membranous nephropathy: A 6-month trial with extended follow-up. J Am Soc Nephrol28: 348–358, 2017PubMed
DahanK, DebiecH, PlaisierE, CachanadoM, RousseauA, WakselmanL, ; GEMRITUX Study Group: Rituximab for severe membranous nephropathy: A 6-month trial with extended follow-up. J Am Soc Nephrol 28: 348–358, 2017PubMed)| false
FervenzaFC, AppelGB, BarbourSJ, RovinBH, LafayetteRA, AslamN, et al.; MENTOR Investigators: Rituximab or cyclosporine in the treatment of membranous nephropathy. N Engl J Med381: 36–46, 2019PubMed
FervenzaFC, AppelGB, BarbourSJ, RovinBH, LafayetteRA, AslamN, ; MENTOR Investigators: Rituximab or cyclosporine in the treatment of membranous nephropathy. N Engl J Med 381: 36–46, 2019PubMed)| false
Fernández-JuárezG, Rojas-RiveraJ, LogtAV, JustinoJ, SevillanoA, Caravaca-FontánF, et al.; STARMEN Investigators: The STARMEN trial indicates that alternating treatment with corticosteroids and cyclophosphamide is superior to sequential treatment with tacrolimus and rituximab in primary membranous nephropathy. Kidney Int99: 986–998, 2021PubMed
Fernández-JuárezG, Rojas-RiveraJ, LogtAV, JustinoJ, SevillanoA, Caravaca-FontánF, ; STARMEN Investigators: The STARMEN trial indicates that alternating treatment with corticosteroids and cyclophosphamide is superior to sequential treatment with tacrolimus and rituximab in primary membranous nephropathy. Kidney Int 99: 986–998, 2021PubMed)| false
ScolariF, DelbarbaE, SantoroD, GesualdoL, PaniA, DalleraN, et al.; RI-CYCLO Investigators: Rituximab or cyclophosphamide in the treatment of membranous nephropathy: The RI-CYCLO randomized trial. J Am Soc Nephrol32: 972–982, 2021PubMed
ScolariF, DelbarbaE, SantoroD, GesualdoL, PaniA, DalleraN, ; RI-CYCLO Investigators: Rituximab or cyclophosphamide in the treatment of membranous nephropathy: The RI-CYCLO randomized trial. J Am Soc Nephrol 32: 972–982, 2021PubMed)| false
SethiS, KumarS, LimK, JordanSC: Obinutuzumab is effective for the treatment of refractory membranous nephropathy. Kidney Int Rep5: 1515–1518, 2020PubMed
SethiS, KumarS, LimK, JordanSC: Obinutuzumab is effective for the treatment of refractory membranous nephropathy. Kidney Int Rep 5: 1515–1518, 2020PubMed)| false