P. Niaudet

R. Salomon, G. Canaud, M. Gubler, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Determinants of eGFR at start of renal replacement therapy in paediatric patients.

A. Jankauskienė, F. Schaefer, J. Groothoff, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Acute kidney injury complicating nephrotic syndrome of minimal change disease.

P. Niaudet, A. Meyrier, 2018, Kidney international.

Acute Kidney Failure and Minimal Change Disease

P. Niaudet, A. Meyrier, 2018 .

Causes of death in pediatric systemic lupus erythematosus.

B. Bader-Meunier, A. Belot, P. Quartier, 2009, Clinical and experimental rheumatology.

Pulse cyclophosphamide therapy and clinical remission in atypical hemolytic uremic syndrome with anti-complement factor H autoantibodies.

R. Salomon, P. Niaudet, V. Frémeaux-Bacchi, 2010, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Rituximab therapy for childhood-onset systemic lupus erythematosus.

E. Haddad, R. Salomon, T. Leblanc, 2006, The Journal of pediatrics.

CHAPTER 11 – Nephritic Syndrome

P. Niaudet, 2008 .

[Renal involvement in mitochondrial cytopathies].

P. Niaudet, 1996, Nephrologie & therapeutique.

Diabetes mellitus in patients with infantile cystinosis after renal transplantation

P. Niaudet, J. Robert, G. Guest, 1999, Pediatric Nephrology.

Prognosis of autosomal dominant polycystic kidney disease diagnosed in utero or at birth

R. Salomon, P. Niaudet, M. Charbit, 2007, Pediatric Nephrology.

Early-childhood membranous nephropathy due to cationic bovine serum albumin.

G. Remuzzi, G. Deschênes, M. Kemper, 2011, The New England journal of medicine.

Comparison of three low-nitrogen diets containing essential amino acids and their alpha analogues for severely uremic children.

P. Niaudet, M. Broyer, C. Kleinknecht, 1983, Kidney international. Supplement.

A randomised Phase I/II trial to evaluate the efficacy and safety of orally administered Oxalobacter formigenes to treat primary hyperoxaluria

R. Salomon, B. Hoppe, G. Deschênes, 2017, Pediatric Nephrology.

Chronic renal failure after Puumala virus infection

C. Guyot, M. Gubler, P. Niaudet, 1999, Pediatric Nephrology.

Acute lymphoblastic leukaemia associated antigen—II. Isolation and partial characterisation

M. Greaves, R. Sutherland, P. Niaudet, 1978 .

Lung manifestations in MPO‐ANCA associated vasculitides in children

C. Delacourt, P. Niaudet, A. Hadchouel, 2014, Pediatric pulmonology.

Hemolytic Uremic Syndrome: New Developments in Pathogenesis and Treatment

P. Niaudet, O. Boyer, 2011, International journal of nephrology.

Neurological involvement in a child with atypical hemolytic uremic syndrome

N. Boddaert, P. Niaudet, V. Frémeaux-Bacchi, 2010, Pediatric Nephrology.

Renal involvement in juvenile chronic arthritis: clinical and pathologic features.

A. Prieur, M. Gubler, P. Niaudet, 1987, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Therapeutic approach to focal and segmental glomerulosclerosis recurrence in kidney transplant recipients.

G. Canaud, M. Mamzer, P. Niaudet, 2010, Transplantation reviews.

High serum levels of a non-(1–84) parathyroid hormone (PTH) fragment in pediatric haemodialysis patients

J. Souberbielle, P. Niaudet, M. Charbit, 2001, Pediatric Nephrology.

Molecular identification of human T-lymphocyte antigens defined by the OKT5 and OKT8 monoclonal antibodies.

P. Niaudet, J. Bach, F. Phan-Dinh-Tuy, 1982, Molecular immunology.

Altered Leukotriene Generation in Leukocytes from Cystinotic Children

J. Mencia-Huerta, P. Niaudet, G. Pintos-Morell, 1994, Pediatric Research.

Truncation of cMip ( Tc-mip ) , a new proximal signaling protein , induces c-maf-dependent Th 2 pathway and cytoskeleton reorganization

A. Bensman, D. Sahali, A. Pawlak, 2018 .

Improvement of Renal Function in Pediatric Heart Transplant Recipients Treated with Low-Dose Calcineurin Inhibitor and Mycophenolate Mofetil

M. Gubler, P. Niaudet, M. Déchaux, 2005, Transplantation.

Renal Granulomatous sarcoidosis in childhood: a report of 11 cases and a review of the literature

A. Bensman, P. Niaudet, C. Loirat, 1999, European Journal of Pediatrics.

Ask the expert

P. Niaudet, 2004, Pediatric Nephrology.

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

C. Antignac, L. Guay-Woodford, L. P. Van den Heuvel, 1998, Kidney international.

301 Nephrotic Syndrome in Children

P. Niaudet, 2012 .

Eculizumab in severe Shiga-toxin-associated HUS.

T. Boppel, F. Schaefer, P. Niaudet, 2011, The New England journal of medicine.

Family Outbreak of Shiga Toxin–producing Escherichia coli O123:H–, France, 2009

V. Vaillant, P. Niaudet, H. de Valk, 2010, Emerging infectious diseases.

Haemolytic uraemic syndrome: prognostic factors in children over 3 years of age

P. Niaudet, M. Broyer, R. Habib, 1995, Pediatric Nephrology.

The IgE humoral response in OKT3-treated patients. Incidence and fine specificity.

D. Abramowicz, M. Goldman, L. Chatenoud, 1996, Transplantation.

High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis.

O. Gribouval, C. Antignac, P. Niaudet, 1996, American journal of human genetics.

A controlled study of deflazacort in the treatment of idiopathic nephrotic syndrome

F. Terzi, P. Niaudet, G. Guest, 1997, Pediatric Nephrology.

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

O. Gribouval, C. Antignac, P. Niaudet, 2004, Kidney international.

Strict blood-pressure control and progression of renal failure in children.

A. Anarat, S. Testa, A. Bakkaloğlu, 2009, The New England journal of medicine.

Tumor cell line characterization of a malignant histiocytosis transplanted into nude mice

P. Niaudet, F. Jaubert, C. Nezelof, 2004, Virchows Archiv A.

Duration of action of a chimeric interleukin-2 receptor monoclonal antibody, basiliximab, in pediatric kidney transplant recipients.

H. Ansart‐Pirenne, P. Niaudet, V. Baudouin, 2000, Transplantation proceedings.

Transcriptional and Post-Transcriptional Alterations of I κBα in Active Minimal-Change Nephrotic Syndrome

G. Guellaen, A. Bensman, D. Sahali, 2001 .

Transcriptional and Post-Transcriptional Alterations of I k B a in Active Minimal-Change Nephrotic Syndrome

G. Guellaen, A. Bensman, D. Sahali, 2001 .

Haemolytic uraemic syndrome and pulmonary hypertension in a patient with methionine synthase deficiency

P. Niaudet, J. Zittoun, J. Marquet, 1999, European Journal of Pediatrics.

Hemolytic-Uremic Syndrome in Children.

P. Niaudet, O. Boyer, 2022, Pediatric clinics of North America.

Activation of Human T Lymphocytes by Soluble Protein A

G. Beaurain, P. Niaudet, 1985, Scandinavian journal of immunology.

Renovascular hypertension and vascular anomalies in Alagille syndrome

J. Sarles, P. Niaudet, M. Hadchouel, 1998, Pediatric Nephrology.

Side effects of levamisole in children with nephrosis

P. Niaudet, J. Palcoux, P. Goumy, 1994, Pediatric Nephrology.

Somatostatin Secretion in Children on CAPD and CCPD

P. Niaudet, M. Broyer, B. Roth, 1985 .

Protein Losses During Peritoneal Dialysis in Children

P. Niaudet, M. Broyer, R. Drachman, 1985 .

Increased monocyte-dependent suppression of polyclonal activation of B lymphocytes from cystinotic children

P. Niaudet, G. Pintos-Morell, M. Déchaux, 1991, Pediatric Nephrology.

Altered Oxidative Metabolism, Motility, and Adherence in Phagocytic Cells from Cystinotic Children

B. Descamps-Latscha, P. Niaudet, G. Jean, 1985, Pediatric Research.

Glomerular Lesions in Patients With Sickle Cell Disease

O. Lambotte, P. Lang, P. Niaudet, 2010, Medicine.

Nutritional and metabolic studies in children on continuous ambulatory peritoneal dialysis.

P. Czernichow, P. Niaudet, M. Broyer, 1983, Kidney international. Supplement.

Loss of Ultrafiltration and Peritoneal Membrane Alterations in Children on CAPD

M. Gubler, P. Niaudet, M. Broyer, 1985 .

Modification of peritoneal ultrafiltration capacity in children undergoing peritoneal dialysis.

P. Niaudet, M. Broyer, R. Drachman, 1985, The International journal of pediatric nephrology.

Cyclosporin therapy in patients with Alport syndrome

M. Gubler, J. Grünfeld, P. Niaudet, 2007, Pediatric Nephrology.

Effect of plasma protein adsorption on protein excretion in kidney-transplant recipients with recurrent nephrotic syndrome

P. Niaudet, B. Charpentier, J. Soulillou, 1994, Pediatric Nephrology.

de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency.

B. Poll-The, P. Niaudet, J. Saudubray, 1988, The Journal of pediatrics.

Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults.

L. Rostaing, F. Bienaimé, G. Deschênes, 2013, Clinical journal of the American Society of Nephrology : CJASN.

WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis.

E. Denamur, R. Veitia, M. Gubler, 2000, Kidney international.

Everolimus in pediatric de nova renal transplant patients1

J. Kovarik, P. Niaudet, J. Mahan, 2003, Transplantation.

Growth in boys with idiopathic nephrotic syndrome on long-term cyclosporin and steroid treatment

P. Czernichow, G. Deschênes, P. Niaudet, 2009, Pediatric Nephrology.

Treatment of idiopathic nephrotic syndrome with cyclosporin in children. Preliminary results of growth data in long-term use.

P. Niaudet, M. Broyer, R. Habib, 1992, Journal of autoimmunity.

Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits.

R. Salomon, P. Niaudet, V. Frémeaux-Bacchi, 2008, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Eculizumab for Atypical Hemolytic Uremic Syndrome Recurrence in Renal Transplantation

G. Ardissino, N. Heyne, C. Legendre, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Renal Transplantation Under Prophylactic Eculizumab in Atypical Hemolytic Uremic Syndrome With CFH/CFHR1 Hybrid Protein

P. Niaudet, D. Beury, V. Frémeaux-Bacchi, 2012, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

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

P. Niaudet, C. Loirat, 2003, Pediatric Nephrology.

Congenital nephrotic syndrome, Finnish type

P. Niaudet, 2004 .

Non-immunologic mechanisms of calcineurin inhibitors explain its antiproteinuric effects in genetic glomerulopathies

A. Bensman, P. Niaudet, 2010, Pediatric Nephrology.

Cyclosporine in the treatment of idiopathic nephrosis.

P. Niaudet, R. Habib, 1994, Journal of the American Society of Nephrology : JASN.

Nephrogenic diabetes insipidus: clinical and pathophysiological aspects.

P. Niaudet, C. Loirat, M. Broyer, 1984, Advances in nephrology from the Necker Hospital.

Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome.

W. Fridman, A. Bagga, H. Cheong, 2010, Journal of the American Society of Nephrology : JASN.

Safety and tolerability of cyclosporin A (Sandimmun®) in idiopathic nephrotic syndrome

C. Ponticelli, G. Feutren, P. Niaudet, 1991 .

Utility of genetic screening in children with nephrotic syndrome presenting during the first year of life

P. Niaudet, 2007, Nature Clinical Practice Nephrology.

Postransplant lymphoproliferative disease following renal transplantation: a multicenter retrospective study of 41 cases observed between 1992 and 1996. French Speaking Transplantation Workshop.

P. Niaudet, 1998, Transplantation proceedings.

Optimal Use of Sandimmun® in Nephrotic Syndrome

P. Niaudet, A. Meyrier, J. Brodehl, 1992, Springer Berlin Heidelberg.

Nephrotic syndrome: Rituximab in childhood steroid-dependent nephrotic syndrome

P. Niaudet, O. Boyer, 2013, Nature Reviews Nephrology.

Outcome of children with acute renal failure.

P. Niaudet, M. Broyer, M. Gagnadoux, 1985, Kidney international. Supplement.

Long-term evaluation of Ifosfamide-related nephrotoxicity in children.

G. Leverger, D. Orbach, P. Niaudet, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Tubulopathy and pancytopaenia with normal pancreatic function: a variant of Pearson syndrome.

A. Fischer, A. Munnich, A. Rötig, 2009, European journal of medical genetics.

Differences in effect of isoproterenol stimulation on levels of cyclic AMP in human B and T lymphocytes

G. Beaurain, P. Niaudet, M. Bach, 1976, European journal of immunology.

Renal Involvement in Children with Systemic Lupus Erythematosus

R. Salomon, B. Bader-Meunier, P. Niaudet, 2015 .

Kidney transplantation in children: results of 383 grafts performed at Enfants Malades Hospital from 1973 to 1984.

P. Niaudet, M. Busson, G. Guest, 1987, Advances in nephrology from the Necker Hospital.

Primary hyperoxaluria Author : Professor

P. Niaudet, 2004 .

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

Pierre Cochat, Bernd Hoppe, B. Hoppe, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Pediatric Nephrology

P. Niaudet, W. Harmon, 1981, Developments in Nephrology.

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

Y. Révillon, P. Niaudet, P. Jouvet, 2001, Pediatric Nephrology.

Papillary stones with Randall's plaques in children: clinicobiological features and outcome.

R. Salomon, M. Daudon, P. Niaudet, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Hair and skin disorders as signs of mitochondrial disease.

C. Bodemer, A. Munnich, P. Rustin, 1999, Pediatrics.

A new gel formulation of topical cysteamine for the treatment of corneal cystine crystals in cystinosis: the Cystadrops OCT-1 study.

G. Deschênes, P. Niaudet, C. Baudouin, 2014, Molecular genetics and metabolism.

Nephropathic cystinosis: an international consensus document.

D. Trauner, W. Gahl, C. Antignac, 2014, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Marc Fellous, Ken McElreavey, M. Gubler, 1997, Nature Genetics.

Thymic function in NZB mice. II. Regulatory influence of a circulating thymic factor on antibody production against polyvinylpyrrolidone in NZB mice.

P. Niaudet, M. Bach, 1976, Journal of immunology.

Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults.

C. Antignac, P. Niaudet, A. Servais, 2012, Kidney international.

Full Review Nephropathic cystinosis: an international consensus document

D. Trauner, W. Gahl, C. Antignac, 2014 .

A randomized controlled crossover trial with delayed-release cysteamine bitartrate in nephropathic cystinosis: effectiveness on white blood cell cystine levels and comparison of safety.

Larry A Greenbaum, Pierre Cochat, Georges Deschênes, 2012, Clinical journal of the American Society of Nephrology : CJASN.

In vivo reflectance confocal microscopy of the skin: a noninvasive means of assessing body cystine accumulation in infantile cystinosis.

C. Chiaverini, P. Bahadoran, J. Ortonne, 2013, Journal of the American Academy of Dermatology.

Cystinosin is a melanosomal protein that regulates melanin synthesis

K. Wakamatsu, S. Ito, C. Chiaverini, 2012, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

An international cohort study spanning five decades assessed outcomes of nephropathic cystinosis.

L. Ravà, C. Antignac, O. Devuyst, 2021, Kidney international.

Excellent long-term outcome of renal transplantation in cystinosis patients

B. Chadefaux-Vekemans, M. Kessler, P. Niaudet, 2015, Orphanet Journal of Rare Diseases.

Outcome of infantile nephropathic cystinosis depends on early intervention, not genotype: A multicenter sibling cohort study

D. Haffner, E. Levtchenko, G. Ariceta, 2022, Journal of inherited metabolic disease.

Cystinose et syndrome de Fanconi

P. Niaudet, 2012 .

Immunological factors in organ transplantation

P. Niaudet, 2004, Intensive Care Medicine.

Non-immunological risk factors in paediatric renal transplantation

P. Niaudet, M. Broyer, M. Gagnadoux, 1993, Pediatric Nephrology.

Treatment and outcome of congenital nephrotic syndrome

R. Salomon, O. Gribouval, J. Bacchetta, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Long-term results of renal transplantation in children with the prune-belly syndrome.

L. Salomon, P. Niaudet, M. Broyer, 1997, The Journal of urology.

Development of human renal function: reference intervals for 10 biochemical markers in fetal urine.

L. Bussières, P. Aegerter, Y. Aigrain, 1996, Clinical chemistry.

Management of oxalosis.

Y. Révillon, M. Daudon, P. Niaudet, 1996, Kidney international. Supplement.

A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure

A. Munnich, P. Rustin, A. Rötig, 2001, Nature Genetics.

Renal involvement in mitochondrial cytopathies

A. Rötig, P. Niaudet, 1996, Pediatric Nephrology.

Deletion of the mitochondrial DNA in a case of de Toni-Debré-Fanconi syndrome and Pearson syndrome

A. Munnich, A. Rötig, M. Gubler, 1994, Pediatric Nephrology.

The kidney in mitochondrial cytopathies.

A. Rotig, P. Niaudet, 1997, Kidney international.

Anti-B-cell monoclonal antibodies in the treatment of severe B-cell lymphoproliferative syndrome following bone marrow and organ transplantation.

A. Fischer, C. Griscelli, P. Niaudet, 1991, The New England journal of medicine.

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.

C. Guyot, X. Jeunemaître, G. Deschênes, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Comparison between pre- and posttreatment renal biopsies in children receiving ciclosporine for idiopathic nephrosis.

P. Niaudet, R. Habib, 1994, Clinical nephrology.

NPHS 2 , encoding the glomerular protein podocin , is mutated in autosomal recessive steroid-resistant nephrotic syndrome

K. Dahan, O. Gribouval, C. Antignac, 2000 .

In vitro characteristics on human lymphocyte functions of a new immunomodulatory agent, a cyclic peptide, cyclomunine.

G. Beaurain, P. Niaudet, J. Bach, 1980, Clinical and experimental immunology.

Intra‐ and postoperative adverse events in children with nephrotic syndrome requiring surgery under general anesthesia

P. Niaudet, P. Carli, G. Orliaguet, 2012, Paediatric anaesthesia.

Congenital nephrotic syndrome , Finnish type Author : Professor

P. Niaudet, 2004 .

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.

J. Lamerdin, A. Olsen, O. Gribouval, 1999, American journal of human genetics.

Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.

T. Benzing, O. Gribouval, C. Antignac, 2008, Journal of the American Society of Nephrology : JASN.

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

J. Beckmann, O. Gribouval, C. Antignac, 1995, Human molecular genetics.

Steroid-sensitive nephrotic syndrome: from childhood to adulthood.

Paul Landais, Bertrand Knebelmann, B. Knebelmann, 2003, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Long-term outcome of children with steroid-sensitive idiopathic nephrotic syndrome.

P. Niaudet, 2009, Clinical journal of the American Society of Nephrology : CJASN.

A randomized clinical trial indicates that levamisole increases the time to relapse in children with steroid-sensitive idiopathic nephrotic syndrome.

A. Bagga, M. Van Dyck, F. Emma, 2017, Kidney international.

Treatment of severe childhood nephrosis.

P. Niaudet, M. Broyer, R. Habib, 1988, Advances in nephrology from the Necker Hospital.

Mycophenolate mofetil for steroid-dependent nephrotic syndrome: a phase II Bayesian trial

G. Deschênes, A. Bensman, F. Broux, 2012, Pediatric Nephrology.

Nephrotic syndrome in children.

P. Niaudet, 1993, Current opinion in pediatrics.

Cyclosporin in the treatment of idiopathic nephrotic syndrome in children

P. Niaudet, M. Broyer, R. Habib, 1987, Pediatric Nephrology.

Long-term outcome in methylmalonic aciduria: a series of 30 French patients.

N. Boddaert, Philippe M. Campeau, D. Rabier, 2009, Molecular genetics and metabolism.

Nephronophthisis

Sophie Saunier, Rémi Salomon, R. Salomon, 2008, Pediatric Nephrology.

Surface markers and electron microscopy of human blood L cells: a comparison with T and B lymphocytes.

M. Greaves, P. Niaudet, P. Deteix, 1978, Journal of immunology.

Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria.

A. Munnich, C. Guyot, D. Rabier, 2008, Molecular genetics and metabolism.

Steroid-Sensitive Nephrotic Syndrome

A. Bagga, P. Niaudet, A. Swiatecka-Urban, 2021, Pediatric Nephrology.

Treatment of idiopathic nephrotic syndrome with cyclosporin A in children.

P. Niaudet, M. Broyer, R. Habib, 1991, Clinical nephrology.

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

K. Dahan, R. Salomon, O. Gribouval, 2018, Pediatric Nephrology.

Urological complications after renal transplantation using ureteroureteral anastomosis in children.

Y. Révillon, P. Niaudet, M. Charbit, 2001, Journal of Urology.

Small intestinal transplantation in a child using cyclosporine.

A. Fischer, Y. Révillon, O. Goulet, 1988, Transplantation proceedings.

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

Colin A. Johnson, Nathalie Boddaert, Sophie Saunier, 2007, Nature Genetics.

Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1

K. Dahan, P. Houillier, X. Jeunemaître, 2015, Human mutation.

Anti-OKT3 response following prophylactic treatment in paediatric kidney transplant recipients

L. Chatenoud, P. Niaudet, M. Broyer, 1993, Pediatric Nephrology.

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.

J. Grünfeld, P. Niaudet, A. Servais, 2012, Kidney international.

Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease.

V. Torres, P. Harris, K. Hopp, 2009, Kidney international.

Long-term follow-up of ifosfamide renal toxicity in children treated for malignant mesenchymal tumors: an International Society of Pediatric Oncology report.

P. Niaudet, F. Flamant, E. Comoy, 1991, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database.

E. Denamur, C. Junien, M. Gubler, 1998, American journal of human genetics.

Living donor kidney transplantation in patients with hereditary nephropathies

P. Niaudet, 2010, Nature Reviews Nephrology.

Different inactivating mutations of the mineralocorticoid receptor in fourteen families affected by type I pseudohypoaldosteronism.

R. Salomon, D. Armanini, M. Lombès, 2003, Journal of Clinical Endocrinology and Metabolism.

A rational dosing algorithm for basiliximab (Simulect) in pediatric renal transplantation based on pharmacokinetic-dynamic evaluations1

J. Kovarik, P. Niaudet, M. Hall, 2002, Transplantation.

A multicenter, open-label, pharmacokinetic/pharmacodynamic safety, and tolerability study of basiliximab (Simulect) in pediatric de novo renal transplant recipients

P. Niaudet, M. Hall, P. Cochat, 2002, Transplantation.

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

X. Estivill, M. Caulfield, P. Froguel, 2012, Nature Genetics.

High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations.

K. Tory, N. Boddaert, R. Salomon, 2007, Journal of the American Society of Nephrology : JASN.

Impairment of lung diffusion capacity in Schönlein-Henoch purpura.

D. De boissieu, P. Niaudet, G. Kalifa, 1992, The Journal of pediatrics.

Population Pharmacokinetics and Pharmacogenetics of Mycophenolic Acid Following Administration of Mycophenolate Mofetil in De Novo Pediatric Renal‐Transplant Patients

G. Deschênes, A. Bensman, P. Niaudet, 2010, Journal of clinical pharmacology.

Peanut Agglutinin

P. Niaudet, L. Laroche, J. London, 1978, Scandinavian journal of immunology.

Pretransplant blood transfusions with cyclosporine in pediatric renal transplantation

P. Niaudet, M. Charbit, J. Dudley, 2000, Pediatric Nephrology.

Renal transplantation in 4 patients with methylmalonic aciduria: a cell therapy for metabolic disease.

R. Salomon, D. Rabier, Y. Aigrain, 2013, Molecular genetics and metabolism.

Successful kidney transplantation of immunized patients after desensitization with normal human polyclonal immunoglobulins.

J. Haymann, J. Bariéty, P. Niaudet, 1995, Transplantation proceedings.

Detection of antilineage specific leucocyte antibodies by a quantitative immunocytometry method in sera from candidates for renal allografts.

P. Niaudet, C. Kaplan, M. Broyer, 1995, Transplant immunology.

Population Pharmacokinetics and Pharmacogenetics of Tacrolimus in De Novo Pediatric Kidney Transplant Recipients

A. Bensman, P. Niaudet, G. Roussey, 2009, Clinical pharmacology and therapeutics.

PREGNANCY AND GLOMERULONEPHRITIS

P. Niaudet, F. Guillot, P. Lang, 1989, The Lancet.

X‐linked hypohidrotic ectodermal dysplasia and t(X;12) in a female

M. Cabanis, P. Niaudet, D. Cau, 1989, Clinical genetics.

Diffuse arterial calcified elastopathy--a new cause of renovascular hypertension in children.

C. Antignac, M. Gubler, L. Garel, 1985, The International journal of pediatric nephrology.

Methylprednisolone pulse therapy in the treatment of severe forms of Schönlein-Henoch purpura nephritis

P. Niaudet, Patrick Niaudet, R. Habib, 1998, Pediatric Nephrology.

LONG-TERM SOCIAL OUTCOME OF CHILDREN AFTER KIDNEY TRANSPLANTATION

P. Niaudet, M. Charbit, G. Guest, 2004, Transplantation.

Primary IgA nephropathies in children: prognosis and treatment.

P. Niaudet, M. Broyer, R. Habib, 1993, Advances in nephrology from the Necker Hospital.

Glucocorticoid pharmacokinetics and growth retardation in children with renal transplants

P. Niaudet, J. Bresson, R. Hankard, 2004, Pediatric Nephrology.

Clinical features and management of arterial hypertension in children with Williams-Beuren syndrome.

F. Brunelle, R. Salomon, G. Landthaler, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

High NPHP 1 and NPHP 6 Mutation Rate in Patients with Joubert Syndrome and Nephronophthisis : Potential Epistatic Effect of NPHP 6 and AHI 1 Mutations in Patients with NPHP 1 Mutations

K. Tory, N. Boddaert, R. Salomon, 2007 .

Comparison of two protein diets in infants with chronic renal failure

F. Terzi, P. Niaudet, M. Broyer, 1995 .

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes.

A. Ziegler, K. Grzeschik, G. Rizzoni, 1997, Human molecular genetics.

Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity

A. Ziegler, G. Rizzoni, C. Antignac, 2019 .

Clinicopathologic correlations in severe forms of Henoch-Schönlein purpura nephritis based on repeat biopsies.

P. Niaudet, M. Lévy, M. Broyer, 1984, Contributions to nephrology.

Multicenter trial of everolimus in pediatric renal transplant recipients: Results at three year

P. Niaudet, J. Mahan, P. Grimm, 2008, Pediatric transplantation.

Steady-state pharmacokinetics of cyclosporine in renal transplant patients: does an influence of age or body weight exist?

P. Niaudet, G. Guest, M. Broyer, 1994, Transplantation proceedings.

Timing and outcome of renal replacement therapy in patients with congenital malformations of the kidney and urinary tract.

C. Wanner, P. Ravani, F. Schaefer, 2013, Clinical journal of the American Society of Nephrology : CJASN.

Nail-patella syndrome

P. Niaudet, 2004 .

Nail-patella syndrome Author : Professor

P. Niaudet, 2004 .

[Renal transplantation in children under five years of age. Experience at the Hopital des Enfants-Malades].

Y. Révillon, P. Niaudet, M. Charbit, 1993, Annales de pediatrie.

Nephrotic syndrome in Kawasaki disease: a report of three cases

P. Niaudet, D. Sidi, O. Boyer, 2012, Pediatric Nephrology.

Renal function and histology in children after small bowel transplantation

M. Gubler, O. Goulet, P. Niaudet, 2013, Pediatric transplantation.

Relapsing nephrotic syndrome

P. Niaudet, 1993 .

[Bacterial complications of nephrotic syndrome in children].

P. Niaudet, P. Cochat, M. Broyer, 1995, Presse medicale.

Recurrence of de novo membranous glomerulonephritis on renal grafts.

P. Niaudet, L. Heidet, M. Broyer, 1994, Clinical nephrology.

PAX2 mutations in oligomeganephronia.

S. Lyonnet, M. Gubler, M. Vekemans, 2001, Kidney international.

One-year routine renal transplant biopsies in children

D. Droz, P. Niaudet, J. P. Benamenyo, 2001, Pediatric nephrology (Berlin, West).

Congenital nephrotic syndrome: commentary

P. Niaudet, 2001, Pediatric Nephrology.

[Transmission of nephrotic syndrome to two neonates. Spontaneous regression].

P. Niaudet, A. Branellec, J. Heslan, 1991, Presse medicale.

H deficiency in two brothers with atypical dense intramembranous deposit disease.

M. Gubler, P. Niaudet, M. Lévy, 1986, Kidney international.

Nitrogen mustard therapy in idiopathic nephrotic syndrome of childhood.

P. Niaudet, M. Broyer, C. Kleinknecht, 1985, The International journal of pediatric nephrology.

Treatment of childhood steroid-resistant idiopathic nephrotic syndrome.

P. Niaudet, M. Broyer, M. Gagnadoux, 1998, Advances in nephrology from the Necker Hospital.

Pediatric nephrology, seventh edition

E. Avner, S. Goldstein, N. Yoshikawa, 2015 .

Congenital disorders of glycosylation type I: a rare but new cause of hyperechoic kidneys in infants and children due to early microcystic changes

L. Hertz-Pannier, F. Brunelle, P. Niaudet, 2006, Pediatric Radiology.

Overall Neutralization of Complement Factor H by Autoantibodies in the Acute Phase of the Autoimmune Form of Atypical Hemolytic Uremic Syndrome

C. Sautès-Fridman, W. Fridman, A. Bagga, 2012, The Journal of Immunology.

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases.

G. Deschênes, P. Niaudet, P. Coppo, 2004, Journal of the American Society of Nephrology : JASN.

Schönlein-Henoch purpura nephritis: pronostic factors and therapy.

P. Niaudet, R. Habib, 1994, Annales de medecine interne.

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

P. Niaudet, 2000, Pediatric nephrology.

Schönlein-Henoch purpura nephritis

P. Niaudet, 1996 .

Loss of graft by chronic rejection in a series of pediatric kidney transplantation: predictive value of biopsy.

D. Droz, P. Niaudet, M. Charbit, 1998, Transplantation proceedings.

Cyclosporin in the Therapy of Idiopathic Nephrotic Syndrome in Children

P. Niaudet, M. Broyer, 1989 .

Keywords Congenital nephrotic syndrome · Diffuse mesangial sclerosis · WT1 gene · Genetic counselling

P. Niaudet, 2001 .

Proteinuria plus positive hepatitis B surface antigen test.

P. Niaudet, 1990, Pediatric nephrology (Berlin, West).

Ask the expert

P. Niaudet, 1990, Pediatric nephrology (Berlin, West).

[Value of cyclosporine in the treatment of the recurrence of nephrosis after renal transplantation].

D. Droz, M. Gubler, B. Ranchin, 1996, Nephrologie.

Preventive treatment of vascular thrombosis after kidney transplantation in children with low molecular weight heparin.

P. Niaudet, M. Broyer, M. Gagnadoux, 1991, Transplantation proceedings.

Loss of Ultrafiltration and Sclerosing Encapsulating Peritonitis in Children Undergoing CAPD/CCPD

P. Niaudet, 1987 .

Hydration measurement by bioimpedance spectroscopy and blood pressure management in children on hemodialysis

R. Salomon, F. Schaefer, P. Niaudet, 2013, Pediatric Nephrology.

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

P. Niaudet, O. Reigneau, H. Humbert, 2001, Pediatric Nephrology.

New Therapies for the Treatment of Idiopathic Nephrotic Syndrome

P. Niaudet, M. Broyer, R. Habib, 1991 .

Steroid-resistant idiopathic nephrotic syndrome and ciclosporin. French Club of Pediatric Nephrology.

P. Niaudet, 1991, Nephron.

Cyclosporine in the therapy of steroid-resistant idiopathic nephrotic syndrome.

P. Niaudet, M. Broyer, A. Fuchshuber, 1997, Kidney international. Supplement.

Podocin and nephrotic syndrome: implications for the clinician.

P. Niaudet, 2004, Journal of the American Society of Nephrology : JASN.

[Renal involvement in autoimmune enteropathies].

O. Goulet, P. Niaudet, S. Blanche, 1993, Annales de pediatrie.

[Acute renal insufficiency in Kawasaki disease].

P. Niaudet, G. Chéron, L. Heidet, 1993, Archives francaises de pediatrie.

Software and database for the analysis of mutations in the human WT1 gene

Christophe Béroud, Claudine Junien, Cécile Jeanpierre, 1998, Nucleic Acids Res..

[Nephropathy of rheumatoid purpura].

P. Niaudet, R. Habib, 1989, Presse medicale.

Cyclosporine and childhood idiopathic nephrosis.

P. Niaudet, M. Broyer, R. Habib, 1988, Transplantation proceedings.

Sclerosing encapsulating peritonitis in children.

Y. Révillon, P. Niaudet, E. Bérard, 1987, Contributions to nephrology.

Risk of primary disease recurrence in pediatric renal transplantation.

D. Droz, M. Gubler, P. Niaudet, 1999, Transplantation proceedings.

A specific glomerular lesion of the graft: allograft glomerulopathy.

C. Antignac, M. Gubler, P. Niaudet, 1993, Kidney international. Supplement.

CONVERSION FROM AZATHIOPRINE TO MYCOPHENOLATE MOFETIL IN PEDIATRIC RENAL TRANSPLANT RECIPIENTS

P. Niaudet, M. Charbit, G. Guest, 1999 .

Long-term remission of atypical HUS with anti-factor H antibodies after cyclophosphamide pulses

R. Salomon, P. Niaudet, V. Frémeaux-Bacchi, 2013, Pediatric Nephrology.

Complications of nephrotic syndrome in children

P. Niaudet, T. Mattoo, M. Kim, 2015 .

Long‐term results of combined liver‐kidney transplantation for primary hyperoxaluria type 1: The French Experience

D. Samuel, K. Boudjema, L. Rostaing, 2014, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

Update and outcome of renal transplant patients with human immunodeficiency virus. The Groupe Cooperatif de Transplantation de I'lle de France.

P. Lang, P. Niaudet, 1991, Transplantation proceedings.

ANCA-associated glomerulonephritis in systemic-onset juvenile idiopathic arthritis.

R. Salomon, A. Prieur, L. Noel, 2012, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Renal failure from mitochondrial cytopathies.

A. Allegra, M. Gubler, M. Buemi, 1997, Nephron.

Mitochondrial disorders and the kidney

P. Niaudet, 1998, Archives of disease in childhood.

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.

T. Friede, J. Ehrich, H. Anders, 2012, Kidney international.

Population pharmacokinetics and pharmacodynamics of cysteamine in nephropathic cystinosis patients

S. Urien, G. Deschênes, B. Chadefaux-Vekemans, 2011, Orphanet journal of rare diseases.

Donor-Specific Blood Transfusion and Renal Graft Survival: A 3-Year Experience in Pediatrics

P. Niaudet, J. Muller, M. Broyer, 1984 .

The levamisole study in steroid sensitive idiopathic nephrotic syndrome (SSINS): inclusion completed

A. Bagga, E. Levtchenko, F. Emma, 2012 .

Immunoglobulin-producing cells in cultured human peripheral blood lymphocytes. Modulation by accessory cells and enhancing effect of polyacrylamide beads.

P. Niaudet, P. Galanaud, J. Preud’homme, 1980, Clinical immunology and immunopathology.

Fanconi syndrome and severe polyuria: an uncommon clinicobiological presentation of a Gitelman syndrome

R. Salomon, P. Niaudet, A. Garnier, 2014, BMC Pediatrics.

Crescentic glomerulonephritis in juvenile chronic arthritis.

A. Prieur, P. Niaudet, A. François, 1996, The Journal of rheumatology.

Lupus érythémateux disséminé chez l'enfant : recommandations concernant les examens à effectuer lors de l'évaluation initiale et du suivi Guidelines about investigations to be performed at the diagnosis and during the follow-up of childhood-onset systemic lupus erythematosus

C. Bodemer, E. Haddad, R. Salomon, 2004 .

Serial renal biopsies in children with idiopathic nephrosis receiving cyclosporin.

P. Niaudet, M. Broyer, R. Habib, 1995, Contributions to Nephrology.

[Analgesia with oxygen-nitrous oxide mixture during percutaneous renal biopsy in children].

P. Niaudet, C. Pietrement, C. Petitjean, 2001, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Kidney involvement in mitochondrial disorders.

T. Bourgeron, A. Munnich, P. Rustin, 1995, Advances in nephrology from the Necker Hospital.

Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis.

A. Munnich, P. Rustin, A. Rötig, 1995, The Journal of pediatrics.

What is the risk that I will transmit nephrotic syndrome to my children, Doctor?

C. Antignac, G. Benoît, P. Niaudet, 2010, NDT plus.

[Cardiovascular impact of end-stage renal insufficiency in children undergoing hemodialysis].

P. Niaudet, D. Bonnet, D. Sidi, 2000, Archives des maladies du coeur et des vaisseaux.

Comprar Pediatric Nephrology | Avner, Ellis D. | 9783540763277 | Springer

E. Avner, N. Yoshikawa, P. Niaudet, 2009 .

Pediatric en bloc kidney transplantation into pediatric recipients: The French experience

P. Niaudet, O. Niel, E. Bérard, 2012, Pediatric transplantation.

Prophylactic OKT3 monoclonal antibody versus antilymphocyte globulins: a prospective, randomized study in 148 first cadaver kidney grafts.

Y. Révillon, P. Niaudet, G. Guest, 1993, Transplantation proceedings.

[A comparative trial of OKT3 and antilymphocyte serum in the preventive treatment of rejection after kidney transplantation in children].

P. Niaudet, M. Broyer, I. Murcia, 1990, Annales de pediatrie.

High-Resolution Mapping oftheGeneforCystinosis, Using Combined Biochemical andLinkage Analysis

O. Gribouval, P. Niaudet, M. Broyer, 1996 .

Idiopathic Nephrotic Syndrome in Children: Clinical Aspects

P. Niaudet, O. Boyer, 2016 .

[Prevention of vascular thromboses after renal transplantation using low molecular weight heparin].

Y. Révillon, P. Niaudet, M. Broyer, 1991, Annales de pediatrie.

A randomized controlled crossover trial with delayed-release cysteamine bitartrate in nephropathic cystinosis: effectiveness on white blood cell cystine levels and comparison of safety.

M. Sarwal, G. Deschênes, P. Rioux, 2012, Clinical journal of the American Society of Nephrology : CJASN.

Early-childhood membranous nephropathy due to cationic bovine serum albumin.

G. Remuzzi, G. Deschênes, M. Kemper, 2011, The New England journal of medicine.

Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults.

L. Rostaing, F. Bienaimé, G. Deschênes, 2013, Clinical journal of the American Society of Nephrology : CJASN.

Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies.

J. Grünfeld, P. Niaudet, A. Servais, 2012, Kidney International.

Complement factor H deficiency and posttransplantation glomerulonephritis with isolated C3 deposits.

R. Salomon, P. Niaudet, V. Frémeaux-Bacchi, 2008, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Long-term outcome of children with steroid-sensitive idiopathic nephrotic syndrome.

P. Niaudet, 2009, Clinical journal of the American Society of Nephrology : CJASN.

Neurological involvement in a child with atypical hemolytic uremic syndrome

N. Boddaert, P. Niaudet, V. Frémeaux-Bacchi, 2010, Pediatric Nephrology.