S. Decramer

Deepak Kumar Sharma, E. Frangou, M. Zacchia, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Even mild cases of paediatric Henoch‐Schönlein purpura nephritis show significant long‐term proteinuria

J. Hogan, G. Deschênes, S. Decramer, 2015, Acta paediatrica.

Mycophenolic acid area under the concentration-time curve is associated with therapeutic response in childhood-onset lupus nephritis

S. Decramer, V. Guigonis, J. Woillard, 2020, Pediatric Nephrology.

Association of kidney biopsy findings with short- and medium-term outcomes in children with moderate-to-severe IgA vasculitis nephritis

M. Boucekine, S. Decramer, V. Guigonis, 2021, European Journal of Pediatrics.

Clinical outcomes in children with Henoch–Schönlein purpura nephritis without crescents

R. Salomon, J. Hogan, G. Deschênes, 2017, Pediatric Nephrology.

Treatment and long-term outcome in primary distal renal tubular acidosis.

F. Trepiccione, G. Gambaro, Z. Gucev, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

An International Cohort Study of Autosomal Dominant Tubulointerstitial Kidney Disease due to REN Mutations Identifies Distinct Clinical Subtypes.

K. Tory, C. Shaw-Smith, A. Jakubowska, 2020, Kidney international.

Renal phenotypes related to hepatocyte nuclear factor-1beta (TCF2) mutations in a pediatric cohort.

C. Bellanné-Chantelot, S. Beaufils, G. Deschênes, 2006, Journal of the American Society of Nephrology : JASN.

Spectrum of HNF1B mutations in a large cohort of patients who harbor renal diseases.

R. Salomon, C. Antignac, B. Knebelmann, 2010, Clinical journal of the American Society of Nephrology : CJASN.

Mycophenolic Acid Pharmacokinetics and Relapse in Children with Steroid-Dependent Idiopathic Nephrotic Syndrome.

P. Marquet, P. Gandia, S. Decramer, 2016, Clinical journal of the American Society of Nephrology : CJASN.

Pharmacokinetics of mycophenolate mofetil in children with lupus and clinical findings in favour of therapeutic drug monitoring.

R. Salomon, P. Marquet, B. Ranchin, 2014, British journal of clinical pharmacology.

Causes of death in pediatric systemic lupus erythematosus.

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

Familial and syndromic lupus share the same phenotype as other early-onset forms of lupus.

F. Rieux-Laucat, Y. Crow, B. Ranchin, 2017, Joint, bone, spine : revue du rhumatisme.

Pre-emptive kidney transplantation is associated with improved graft survival in children: Data from the French renal replacement therapy registry

K. Leffondré, R. Salomon, B. Ranchin, 2017 .

Long-term effects of in utero exposure to cyclosporin A on renal function in the rabbit.

S. Decramer, J. Gouyon, T. Gilbert, 2004, Journal of the American Society of Nephrology : JASN.

Congenital ureteropelvic junction obstruction: human disease and animal models

J. Schanstra, S. Decramer, J. Klein, 2011, International journal of experimental pathology.

Steroid-responsive nephrotic syndrome in a child with juvenile idiopathic arthritis

S. Decramer, K. Brochard, F. Bandin, 2008, Pediatric Nephrology.

Hepatocyte Nuclear Factor-1β Controls Mitochondrial Respiration in Renal Tubular Cells.

N. Chassaing, J. Schanstra, M. Pontoglio, 2017, Journal of the American Society of Nephrology : JASN.

Renal Prognosis in Children With Tubulointerstitial Nephritis and Uveitis Syndrome

J. Bacchetta, J. Hogan, F. Broux, 2021, Kidney International Reports.

Consensus recommendations for diagnosis, management and treatment of Fabry disease in paediatric patients

D. Lacombe, G. Deschênes, S. Decramer, 2019, Clinical Genetics.

Renal outcome of children exposed to cyclosporine in utero.

P. Audra, S. Decramer, P. Cochat, 2004, Transplantation proceedings.

The low affinity p75 neurotrophin receptor is down-regulated in congenital anomalies of the kidney and the urinary tract: Possible involvement in early nephrogenesis.

J. Schanstra, J. Saulnier-Blache, S. Decramer, 2020, Biochemical and biophysical research communications.

Refining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis

N. Klopp, J. Gerss, H. Omran, 2022, Kidney international reports.

Consensus recommendations for diagnosis, management and treatment of Fabry disease in paediatric patients

D. Lacombe, G. Deschênes, S. Decramer, 2019, Clinical genetics.

Diagnosis, management, and prognosis of HNF1B nephropathy in adulthood.

P. Calvas, N. Chassaing, K. Dahan, 2011, Kidney international.

[Atypical onset of Churg and Strauss syndrome in a child].

A. Garnier, S. Decramer, A. Dallocchio, 2012, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

The ANTENATAL multicentre study to predict postnatal renal outcome in fetuses with posterior urethral valves: objectives and design

J. Schanstra, D. Oepkes, E. Levtchenko, 2019, Clinical kidney journal.

Benign and malignant proliferation in idiopathic nephrotic syndrome: a French cohort study

F. Rieux-Laucat, G. Roussey, S. Decramer, 2022, Pediatric Nephrology.

Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

F. Trepiccione, P. Houillier, L. Weber, 2022, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[Outcomes of pediatric renal transplantation in France].

G. Roussey-Kesler, S. Decramer, 2011, Nephrologie & therapeutique.

Thrombotic microangiopathy in a child with acute pancreatitis.

S. Decramer, A. Breton, P. Broué, 2007, Journal of pediatric gastroenterology and nutrition.

Long-term outcome of children treated with rituximab for idiopathic nephrotic syndrome

A. Garnier, S. Decramer, V. Guigonis, 2013, Pediatric Nephrology.

Quality of life in children with severe forms of idiopathic nephrotic syndrome in stable remission—A cross‐sectional study

G. Deschênes, S. Decramer, T. Ulinski, 2019, Acta paediatrica.

Adverse events associated with currently used medical treatments for cystinuria and treatment goals: results from a series of 442 patients in France

J. Jais, M. Daudon, P. Meria, 2019, BJU international.

CKD and Its Risk Factors among Patients with Cystinuria.

M. Daudon, P. Meria, O. Traxer, 2015, Clinical journal of the American Society of Nephrology : CJASN.

Age‐specific characteristics of neutrophilic dermatoses and neutrophilic diseases in children

S. Mallet, S. Barbarot, J. Lacour, 2019, Journal of the European Academy of Dermatology and Venereology : JEADV.

Preemptive Kidney Transplantation Is Associated With Transplantation Outcomes in Children: Results From the French Kidney Replacement Therapy Registry

K. Leffondré, R. Salomon, C. Couchoud, 2021, Transplantation.

Cryptosporidiosis in paediatric renal transplantation

A. Garnier, S. Decramer, V. Guigonis, 2009, Pediatric Nephrology.

Cryptosporidium spp. Infection in Solid Organ Transplantation: The Nationwide “TRANSCRYPTO” Study

M. Mamzer-Bruneel, O. Lortholary, M. Bougnoux, 2017, Transplantation.

Prospective, Randomized Trial Comparing Short and Long Intravenous Antibiotic Treatment of Acute Pyelonephritis in Children: Dimercaptosuccinic Acid Scintigraphic Evaluation at 9 Months

C. Guyot, S. Decramer, M. Fischbach, 2008, Pediatrics.

Pediatric ANCA vasculitis: clinical presentation, treatment, and outcomes in a French retrospective study

B. Ranchin, C. Dossier, A. Belot, 2023, Pediatric Nephrology.

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.

Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease.

A. Raaijmakers, J. Oury, R. Favre, 2020, Kidney international.

The human urinary proteome reveals high similarity between kidney aging and chronic kidney disease

H. Mischak, J. Coon, M. Dakna, 2009, Proteomics.

Urine in Clinical Proteomics*

Harald Mischak, Joost P. Schanstra, Bernard Monsarrat, 2008, Molecular & Cellular Proteomics.

Combination of the fetal urinary metabolome and peptidome for the prediction of postnatal renal outcome in fetuses with PUV.

J. Schanstra, P. Moulos, S. Decramer, 2018, Journal of proteomics.

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.

Label-free Quantitative Urinary Proteomics Identifies the Arginase Pathway as a New Player in Congenital Obstructive Nephropathy*

B. Monsarrat, J. Schanstra, O. Burlet-Schiltz, 2014, Molecular & Cellular Proteomics.

Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.

R. Salomon, C. Férec, D. Mekahli, 2016, Journal of the American Society of Nephrology : JASN.

Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies plastin 3 as a protein involved in glomerular integrity

B. Wirth, J. Schanstra, O. Burlet-Schiltz, 2021, The Journal of pathology.

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

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

In utero exposure to immunosuppressive drugs: experimental and clinical studies

S. Decramer, J. Gouyon, A. Tendron, 2002, Pediatric Nephrology.

School level of children carrying a HNF1B variant or a deletion

N. Chassaing, C. Bellanné-Chantelot, F. Broux, 2019, European Journal of Human Genetics.

School level of children carrying a HNF1B variant or a deletion

N. Chassaing, C. Bellanné-Chantelot, F. Broux, 2019, European Journal of Human Genetics.

The HNF1B score is a simple tool to select patients for HNF1B gene analysis.

P. Calvas, N. Chassaing, J. Schanstra, 2014, Kidney international.

Expression of Renal Cystic Genes in Patients with HNF1B Mutations

O. Devuyst, D. Chauveau, S. Decramer, 2012, Nephron Clinical Practice.

Mutations in the RARE and MARE regulatory sequences of HNF1β are not a frequent cause of kidney/urinary tract malformation

N. Chassaing, D. Chauveau, S. Decramer, 2009, NDT plus.

Blockade of the kinin B1 receptor ameloriates glomerulonephritis.

D. Salant, J. Schanstra, P. Heeringa, 2010, Journal of the American Society of Nephrology : JASN.

Diagnosis of Streptococcus pneumoniae–associated Hemolytic Uremic Syndrome

S. Decramer, M. Thouret, V. Guigonis, 2013, The Pediatric infectious disease journal.

Patterns of Clinical Response to Eculizumab in Patients With C3 Glomerulopathy.

E. Daugas, A. Servais, S. Decramer, 2018, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Varicella-zoster virus meningoencephalitis without skin lesions in a paediatric kidney recipient.

F. Frascari, A. Garnier, S. Decramer, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[Lowe syndrome revealed by prenatal diagnosis of congenital cataract with brain abnormalities].

S. Decramer, C. Vayssière, A. Sartor, 2014, Gynecologie, obstetrique & fertilite.

Clinical and Genetic Spectrum of Bartter Syndrome Type 3.

B. Knebelmann, G. Deschênes, S. Lemoine, 2017, Journal of the American Society of Nephrology : JASN.

Definition, diagnosis and management of fetal lower urinary tract obstruction: consensus of the ERKNet CAKUT-Obstructive Uropathy Work Group

J. Schanstra, M. Liebau, F. Schaefer, 2022, Nature Reviews Urology.

Mutations affecting the conserved acidic WNK1 motif cause inherited hyperkalemic hyperchloremic acidosis.

P. Welling, X. Jeunemaître, G. Gamba, 2020, The Journal of clinical investigation.

Hepatocyte nuclear factor‐1β shapes the energetic homeostasis of kidney tubule cells

J. Schanstra, D. Chauveau, M. Malet‐Martino, 2021, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts.

R. Moots, R. Redon, I. Bruce, 2020, The Lancet. Rheumatology.

Large-scale analysis of the genetic basis of pediatric systemic lupus erythematosus

Quentin, Y. Crow, Emilie Chopin, 2020 .

A rare cause of anaemia associated with hypertension in a 14-year-old girl

C. Baunin, S. Decramer, G. Ssi-Yan-Kai, 2012, Pediatric Radiology.

Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study.

R. Salomon, B. Ranchin, G. Deschênes, 2015, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Systems biology combining human- and animal-data miRNA and mRNA data identifies new targets in ureteropelvic junction obstruction

Panagiotis Moulos, Julie Klein, Joost Schanstra, 2017, BMC Systems Biology.

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.

Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

N. Boddaert, D. Magen, P. Revy, 2019, Nature Communications.

Alternative complement pathway hemolytic assays reveal incomplete complement blockade in patients treated with eculizumab.

D. Chauveau, A. Blancher, N. Kamar, 2017, Clinical immunology.

The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results

G. Capasso, G. Remuzzi, J. Wetzels, 2021, Orphanet Journal of Rare Diseases.

Valganciclovir is not associated with decreased EBV infection rate in pediatric kidney transplantation

G. Roussey, S. Decramer, V. Baudouin, 2023, Frontiers in Pediatrics.

A low molecular weight urinary proteome profile of human kidney aging

H. Mischak, J. Coon, M. Dakna, 2016 .

A database of naturally occurring human urinary peptides and proteins for use in clinical applications

A. Dominiczak, A. Ganser, W. Kolch, 2007 .

Ofatumumab treatment for nephrotic syndrome recurrence after pediatric renal transplantation

J. Dantal, G. Roussey, S. Decramer, 2020, Pediatric Nephrology.

To biopsy or not to biopsy: Henoch-Schönlein nephritis in children, a 5-year follow-up study

R. Salomon, J. Bacchetta, J. Hogan, 2021, Pediatric Nephrology.

Value of biomarkers for predicting immunoglobulin A vasculitis nephritis outcome in an adult prospective cohort

R. Salomon, E. Daugas, A. Jamin, 2017, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Urinary proteome analysis identifies infants but not older children requiring pyeloplasty

H. Mischak, E. Schiffer, J. Ehrich, 2010, Pediatric Nephrology.

Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome.

R. Salomon, G. Deschênes, F. Broux, 2017, Clinical journal of the American Society of Nephrology : CJASN.

Fetal Urinary Peptides to Predict Postnatal Outcome of Renal Disease in Fetuses with Posterior Urethral Valves (PUV)

H. Mischak, M. Dakna, B. Monsarrat, 2013, Science Translational Medicine.

Update of PAX2 mutations in renal coloboma syndrome and establishment of a locus‐specific database

Marni J. Falk, Gerard C. P. Schaafsma, R. Kumar, 2012, Human mutation.

Long-term effects of cyclophosphamide therapy in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome.

B. Ranchin, S. Decramer, F. Bouissou, 2011, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Comparison of the amniotic fluid and fetal urine peptidome for biomarker discovery in renal developmental disease

J. Schanstra, P. Zürbig, S. Decramer, 2020, Scientific Reports.

A single-center study to evaluate the efficacy of a fetal urine peptide signature predicting postnatal renal outcome in fetuses with posterior urethral valves

J. Schanstra, M. Tkaczyk, S. Decramer, 2019, Pediatric Nephrology.

Klein Fetuses with Posterior Urethral Valves ( PUV ) Fetal Urinary Peptides to Predict Postnatal Outcome of Renal Disease in

H. Mischak, M. Dakna, B. Monsarrat, 2013 .

Hyperechogenic kidneys and polyhydramnios associated with HNF1B gene mutation

R. Salomon, G. Chalouhi, S. Decramer, 2016, Pediatric Nephrology.

Urinary proteome signature of Renal Cysts and Diabetes syndrome in children

G. Remuzzi, H. Mischak, J. Schanstra, 2019, Scientific Reports.

Advances in urinary proteome analysis and biomarker discovery in pediatric renal disease

H. Mischak, J. Ehrich, J. Schanstra, 2010, Pediatric Nephrology.