Interventions for idiopathic steroid-resistant nephrotic syndrome in children. (Q38801673)

6 September 2017

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title

Interventions for idiopathic steroid-resistant nephrotic syndrome in children (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

13 May 2020

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4

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13 May 2020

author name string

Elisabeth M Hodson

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

13 May 2020

Sophia C Wong

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

13 May 2020

Narelle S Willis

series ordinal

3

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13 May 2020

publication date

11 October 2016

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Cochrane Database of Systematic Reviews

6 September 2017

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

13 May 2020

volume

10

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

13 May 2020

page(s)

CD003594

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

Cyclosporin A is superior to cyclophosphamide in children with steroid-resistant nephrotic syndrome-a randomized controlled multicentre trial by the Arbeitsgemeinschaft für Pädiatrische Nephrologie

13 May 2020

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Efficacy and safety of tacrolimus versus cyclosporine in children with steroid-resistant nephrotic syndrome: a randomized controlled trial

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Intravenous pulse cyclophosphamide--a new regime for steroid-resistant minimal change nephrotic syndrome.

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Association of histologic variants in FSGS clinical trial with presenting features and outcomes

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Patient recruitment into a multicenter randomized clinical trial for kidney disease: report of the focal segmental glomerulosclerosis clinical trial (FSGS CT).

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Clinical trial of focal segmental glomerulosclerosis in children and young adults

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Clinical trials treating focal segmental glomerulosclerosis should measure patient quality of life

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Renal function and proteinuria after successful immunosuppressive therapies in patients with FSGS.

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Cyclosporine therapy for steroid-resistant nephrotic syndrome. A controlled study.

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Treatment with tacrolimus and prednisolone is preferable to intravenous cyclophosphamide as the initial therapy for children with steroid-resistant nephrotic syndrome.

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Cyclophosphamide does not benefit patients with focal segmental glomerulosclerosis. A report of the International Study of Kidney Disease in Children.

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Rituximab in children with resistant idiopathic nephrotic syndrome

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Efficacy of intravenous pulse cyclophosphamide treatment versus combination of intravenous dexamethasone and oral cyclophosphamide treatment in steroid-resistant nephrotic syndrome

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Triple immunosuppressive therapy in steroid-resistant nephrotic syndrome children with tacrolimus resistance or tacrolimus sensitivity but frequently relapsing

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A controlled trial of cyclophosphamide and azathioprine in Nigerian children with the nephrotic syndrome and poorly selective proteinuria

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Tacrolimus versus cyclophosphamide in steroid-dependent or steroid-resistant focal segmental glomerulosclerosis: a randomized controlled trial

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Significance of combined cyclosporine-prednisolone therapy and cyclosporine blood concentration monitoring for idiopathic membranous nephropathy with steroid-resistant nephrotic syndrome: a randomized controlled multicenter trial

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A randomized open-label comparative study of conventional therapy versus mizoribine onlay therapy in patients with steroid-resistant nephrotic syndrome (postmarketing survey).

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The effect of treatment of corticosteroid-resistant idiopathic (primary) focal and segmental hyalinosis and sclerosis (focal glomerulosclerosis) with ciclosporin.

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Initial steroid sensitivity in children with steroid-resistant nephrotic syndrome predicts post-transplant recurrence

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Bias in meta-analysis detected by a simple, graphical test

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Nephrotic syndrome in The Netherlands: a population-based cohort study and a review of the literature

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Differential risk of remission and ESRD in childhood FSGS.

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GRADE: an emerging consensus on rating quality of evidence and strength of recommendations

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Treatment of focal glomerulosclerosis with pulse steroids and oral cyclophosphamide

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Long-term outcome of primary nephrotic syndrome

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Treatment of steroid-resistant nephrotic syndrome in children: new guidelines from KDIGO.

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Does quality of reports of randomised trials affect estimates of intervention efficacy reported in meta-analyses?

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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

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Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment effects in controlled trials

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Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort

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Steroid-resistant nephrotic focal segmental glomerulosclerosis: a treatable disease

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Interventions for steroid-resistant nephrotic syndrome: a systematic review

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Interventions for idiopathic steroid-resistant nephrotic syndrome in children

21 January 2018

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Interventions for idiopathic steroid-resistant nephrotic syndrome in children

21 January 2018

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Interventions for idiopathic steroid-resistant nephrotic syndrome in children

21 January 2018

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Predictors of remission and relapse in idiopathic nephrotic syndrome: a prospective cohort study

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Effects of tuna fish oil on hyperlipidemia and proteinuria in childhood nephrotic syndrome

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Older boys benefit from higher initial prednisolone therapy for nephrotic syndrome. The West Japan Cooperative Study of Kidney Disease in Children

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The effects of gemfibrozil on hyperlipidemia in children with persistent nephrotic syndrome

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Effect of fluvastatin and dipyridamole on proteinuria and renal function in childhood IgA nephropathy with mild histological findings and moderate proteinuria.

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Comparative study of angiotensin converting enzyme inhibitor and calcium channel blocker in the treatment of steroid-resistant idiopathic nephrotic syndrome.

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No effect of fluvastatin on the bone mineral density of children with minimal change glomerulonephritis and some focal mesangial cell proliferation, other than an ameliorating effect on their proteinuria

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Treatment of childhood steroid-resistant idiopathic nephrosis with a combination of cyclosporine and prednisone. French Society of Pediatric Nephrology

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Cyclosporin versus cyclophosphamide for patients with steroid-dependent and frequently relapsing idiopathic nephrotic syndrome: a multicentre randomized controlled trial.

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A randomized double-blind placebo-controlled trial of cyclosporine in steroid-resistant idiopathic focal segmental glomerulosclerosis in children

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12 December 2020

10.1002/14651858.CD003594.PUB5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

13 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6457874&resulttype=core&format=json

13 May 2020

1 reference