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Causes of death in pediatric systemic lupus erythematosus

Clinical and experimental rheumatology, 2009-05, Vol.27 (3), p.538

2009

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Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Kidney international, 1998-09, Vol.54 (3), p.720-730

1998

Volltextzugriff (PDF)

Postransplant lymphoproliferative disease following renal transplantation: a multicenter retrospective study of 41 cases observed between 1992 and 1996

Transplantation proceedings, 1998-09, Vol.30 (6), p.2816-2817

Niaudet, P.

1998

Volltextzugriff (PDF)

Podocin and nephrotic syndrome: implications for the clinician

Journal of the American Society of Nephrology, 2004-03, Vol.15 (3), p.832-834

Niaudet, Patrick

2004

Volltextzugriff (PDF)

Efficacy and safety of Oxalobacter formigenes to reduce urinary oxalate in primary hyperoxaluria

Nephrology, dialysis, transplantation, 2011-11, Vol.26 (11), p.3609-3615

2011

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Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

Nature reviews. Nephrology, 2012-11, Vol.8 (11), p.643

2012

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Early Proteinuria Lowering by Angiotensin-Converting Enzyme Inhibition Predicts Renal Survival in Children with CKD

Journal of the American Society of Nephrology, 2018-08, Vol.29 (8), p.2225-2233

2018

Volltextzugriff (PDF)

Mapping a gene (SRN1) to chromosome 1q25–q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis

Human molecular genetics, 1995-11, Vol.4 (11), p.2155-2158

1995

Volltextzugriff (PDF)

A 10-year-old girl was found to have asymptomatic proteinuria upon routine urinary screening at school

Pediatric nephrology (Berlin, West), 2000-01, Vol.14 (1), p.91-91

Niaudet, P

2000

Volltextzugriff (PDF)

Estimating Time to ESRD in Children With CKD

American journal of kidney diseases, 2018-06, Vol.71 (6), p.783-792

2018

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NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Nature genetics, 2000-04, Vol.24 (4), p.349-354

2000

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Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children

Kidney international, 2019-07, Vol.96 (1), p.214-221

2019

Volltextzugriff (PDF)

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence

Kidney international, 2004-08, Vol.66 (2), p.571-579

2004

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Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 cases

Journal of the American Society of Nephrology, 2004-03, Vol.15 (3), p.787-795

2004

Volltextzugriff (PDF)

Henoch-Schönlein purpura

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2006-06, Vol.13 (6), p.599-601

2006

Volltextzugriff (PDF)

Adult social and professional outcomes of pediatric renal transplant recipients

Transplantation, 2014-01, Vol.97 (2), p.196

2014

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The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children

Pediatric nephrology (Berlin, West), 2003-11, Vol.18 (11), p.1095-1101

2003

Volltextzugriff (PDF)

Urological complications after renal transplantation using ureteroureteral anastomosis in children

The Journal of urology, 2001-09, Vol.166 (3), p.1046

2001

Volltextzugriff (PDF)

Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD

Journal of the American Society of Nephrology, 2016-01, Vol.27 (1), p.314-322

2016

Volltextzugriff (PDF)

Congenital nephrotic syndrome: commentary

Pediatric nephrology (Berlin, West), 2001-02, Vol.16 (2), p.190-191

NIAUDET, Patrick

2001

Volltextzugriff (PDF)

A pharmacokinetic study of Neoral in childhood steroid-dependent nephrotic syndrome

Pediatric nephrology (Berlin, West), 2001-02, Vol.16 (2), p.154-155

2001

Volltextzugriff (PDF)

Long term results of liver-kidney transplantation in children with primary hyperoxaluria

Pediatric nephrology (Berlin, West), 2001-12, Vol.16 (12), p.946-950

2001

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The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor

Human mutation, 1999, Vol.13 (2), p.146-153

1999

Volltextzugriff (PDF)

Purpura rhumatoïde

Archives de pédiatrie (Paris), 2006-06, Vol.13 (6), p.599-601

2006

Volltextzugriff (PDF)

Renal histology and response to cyclosporine in childhood idiopathic nephrotic syndrome

Pediatric nephrology (Berlin, West), 1998-11, Vol.12 (9), p.744-745

Niaudet, P

1998

Volltextzugriff (PDF)

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Causes of death in pediatric systemic lupus erythematosus

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Postransplant lymphoproliferative disease following renal transplantation: a multicenter retrospective study of 41 cases observed between 1992 and 1996

Podocin and nephrotic syndrome: implications for the clinician

Efficacy and safety of Oxalobacter formigenes to reduce urinary oxalate in primary hyperoxaluria

Use of eculizumab for atypical haemolytic uraemic syndrome and C3 glomerulopathies

Early Proteinuria Lowering by Angiotensin-Converting Enzyme Inhibition Predicts Renal Survival in Children with CKD

Mapping a gene (SRN1) to chromosome 1q25–q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis

A 10-year-old girl was found to have asymptomatic proteinuria upon routine urinary screening at school

Estimating Time to ESRD in Children With CKD

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence

Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 cases

Henoch-Schönlein purpura

Adult social and professional outcomes of pediatric renal transplant recipients

The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children

Urological complications after renal transplantation using ureteroureteral anastomosis in children

Normal 25-Hydroxyvitamin D Levels Are Associated with Less Proteinuria and Attenuate Renal Failure Progression in Children with CKD

Congenital nephrotic syndrome: commentary

A pharmacokinetic study of Neoral in childhood steroid-dependent nephrotic syndrome

Long term results of liver-kidney transplantation in children with primary hyperoxaluria

The same mutation affecting the splicing of WT1 gene is present on Frasier syndrome patients with or without Wilms' tumor

Purpura rhumatoïde

Renal histology and response to cyclosporine in childhood idiopathic nephrotic syndrome

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