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2014/07/25

Nature Reviews Nephrology - Table of Contents alert Volume 10 Issue 8

Nature Reviews NephrologyInternational Society of Nephrology
 
TABLE OF CONTENTS
 
August 2014 Volume 10 Number 8

Nature Reviews Nephrology cover
Impact Factor 7.943 *
In this issue
Research Highlights
News and Views
Reviews

Also this month
 Featured article:
Next-generation sequencing for research and diagnostics in kidney disease
Kirsten Y. Renkema, Marijn F. Stokman, Rachel H. Giles & Nine V. A. M. Knoers




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RESEARCH HIGHLIGHTS

Top

Nephrotic syndrome: Rituximab is safe and effective in FRNS and SDNS—but where to go from here?
Published online: 08 July 2014
p421 | doi:10.1038/nrneph.2014.119

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Paediatrics: CARPEDIEM—continuous renal replacement therapy for infants
Published online: 10 June 2014
p422 | doi:10.1038/nrneph.2014.100

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Clinical Trials: Off-pump coronary artery bypass graft surgery reduces postoperative AKI risk
Published online: 17 June 2014
p423 | doi:10.1038/nrneph.2014.107

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Genetics: Mapping pathways of CKD
Published online: 01 July 2014
p423 | doi:10.1038/nrneph.2014.117

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Transplantation: IgG reactivity to apoptotic cells—role in presensitization revealed
Published online: 01 July 2014
p423 | doi:10.1038/nrneph.2014.118

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Chronic kidney disease: Targeting connexin-43 reduces progression of CKD in mice
Published online: 10 June 2014
p424 | doi:10.1038/nrneph.2014.101

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Glomerular disease: To the rescue—migrating renin lineage cells heal the injured glomerular mesangium
Published online: 24 June 2014
p424 | doi:10.1038/nrneph.2014.115

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IN BRIEF

From ERA-EDTA—Anaemia: Treating iron deficiency and elevated phosphate—new data | From ERA-EDTA—Transplantation: Calcification propensity associated with renal graft failure | From ERA-EDTA—Diabetic nephropathy: Bardoxolone methyl promotes sodium and fluid retention | From ERA-EDTA—Chronic Kidney Disease: CCL2 inhibition is renoprotective in diabetic nephropathy
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NEWS AND VIEWS

Top
Transplantation: CNIs to mTOR inhibitors—effects on allosensitization?
Aditi Gupta & Bruce Kaplan
Published online: 27 May 2014
p425 | doi:10.1038/nrneph.2014.94
Pre-existing HLA antibodies negatively impact long-term graft survival and might be a major risk factor for the formation of new HLA antibodies. Whether conversion of transplant recipients from calcineurin inhibitors to mammalian target of rapamycin inhibitors increases the risk of allosensitization remains to be determined.
Full Text | PDF


Clinical trials: ISN-ACCTS: global initiatives to improve clinical research
Adeera Levin & Giuseppe Remuzzi
Published online: 10 June 2014
p426 | doi:10.1038/nrneph.2014.98
The International Society of Nephrology-Advisory Committee of Clinical Trials and Studies aims to ensure access to timely and unbiased expert advice for all investigators, and to facilitate the development and execution of clinical trials within a highly ethical framework. The initiative will foster high-quality, cost-effective research in a sustainable network.
Full Text | PDF


Chronic kidney disease: Prenatal risk factors for kidney and urinary tract anomalies
Robert H. Mak & Franz Schaefer
Published online: 17 June 2014
p428 | doi:10.1038/nrneph.2014.105
Childhood-onset chronic kidney disease is the result of congenital anomalies of the kidneys and urinary tract in approximately two-thirds of all patients. An area of intense research in recent years, however, is the potential impact of maternal obesity on renal ontogenesis or postnatal renal function in the offspring.
Full Text | PDF


Transplantation: Molecular diagnosis of kidney transplant rejection
Christian Morath & Martin Zeier
Published online: 17 June 2014
p429 | doi:10.1038/nrneph.2014.106
Acute or chronic antibody-mediated rejection (ABMR) of kidney allografts is currently diagnosed by the presence of donor-specific alloantibodies and distinct pathological findings in biopsy samples. A new study highlights the potential of molecular diagnostics incorporated into standard criteria for acute ABMR to help identify patients at risk of graft loss.
Full Text | PDF


Glomerular disease: The search goes on: suPAR is not the elusive FSGS factor
Jeroen K. Deegens & Jack F. Wetzels
Published online: 24 June 2014
p431 | doi:10.1038/nrneph.2014.113
New research indicates that intact soluble urokinase plasminogen activator receptor (suPAR) does not induce albuminuria in mice. These data corroborate the most recent clinical findings, showing that intact suPAR is not the plasma permeability factor responsible for recurrence of focal segmental glomerulosclerosis after renal transplantation.
Full Text | PDF


 
REVIEWS

Top
Next-generation sequencing for research and diagnostics in kidney disease
Kirsten Y. Renkema, Marijn F. Stokman, Rachel H. Giles & Nine V. A. M. Knoers
Published online: 10 June 2014
p433 | doi:10.1038/nrneph.2014.95
The introduction of next-generation sequencing has provided revolutionary opportunities for comprehensive genetic testing in research and diagnostics. Here, the authors discuss approaches used for novel gene identification, the potential of these techniques to improve the management of patients with inherited kidney diseases—focusing on nephronophthisis and congenital anomalies of the kidney and urinary tract—and the remaining challenges for implementation of next-generation sequencing in clinical practice.
Abstract | Full Text | PDF


Pathology of IgA nephropathy
Ian S. D. Roberts
Published online: 27 May 2014
p445 | doi:10.1038/nrneph.2014.92
In this Review, Ian Roberts provides a detailed description of the immunohistology and light microscopical features of IgA nephropathy, and highlights the importance of accurate recognition of the various histological lesions for reproducible classification of the disease. The different schemas used for classifying IgA nephropathy are compared, with particular focus on the Oxford classification.
Abstract | Full Text | PDF


Renal transplantation in autosomal dominant polycystic kidney disease
Nada Kanaan, Olivier Devuyst & Yves Pirson
Published online: 17 June 2014
p455 | doi:10.1038/nrneph.2014.104
Renal transplantation is the preferred treatment option for patients with autosomal dominant polycystic kidney disease (ADPKD) and end-stage renal disease. Here, the authors discuss special considerations for pretransplant screening and living-related kidney donation in patients with ADPKD, as well as post-transplant outcomes and complications in these patients.
Abstract | Full Text | PDF


Pre-eclampsia part 1: current understanding of its pathophysiology
Tinnakorn Chaiworapongsa, Piya Chaemsaithong, Lami Yeo & Roberto Romero
Published online: 08 July 2014
p466 | doi:10.1038/nrneph.2014.102
Several genetic and environmental factors have been implicated in pre-eclampsia, a rare but serious condition leading to maternal and perinatal morbidity and mortality. In the first of this two-part Review, Chaiworapongsa and colleagues discuss the pathophysiology of pre-eclampsia, including imbalance between angiogenic and antiangiogenic factors, which has emerged as the central pathogenetic mechanism.
Abstract | Full Text | PDF


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