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Anomalies of the TCF2 gene are the main cause of fetal bilateral hyperechogenic kidneys.
Stéphane Decramer
,
Olivier Parant
,
Sandrine Beaufils
,
Séverine Clauin
,
Cécile Guillou
,
et al.
Journal articles
inserm-00409591v1
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Pharmacokinetics of mycophenolate mofetil in children with lupus and clinical findings in favour of therapeutic drug monitoring.
Jean-Baptiste Woillard
,
Brigitte Bader-Meunier
,
Rémi Salomon
,
Bruno Ranchin
,
Stéphane Decramer
,
et al.
Journal articles
inserm-00966145v1
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Is there any relationship between the exposure to mycophenolic acid and the clinical status in children with lupus?
C. Jurado
,
Brigitte Bader-Meunier
,
Bruno Ranchin
,
Stéphane Decramer
,
Michel Fischbac
,
et al.
Pediatric Rheumatology, 2011, 9 (Suppl 1), pp.P248
Journal articles
inserm-00624790v1
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Advances in urinary proteome analysis and biomarker discovery in pediatric renal disease.
Cécile Caubet
,
Chrystelle Lacroix
,
Stéphane Decramer
,
Jens Drube
,
Jochen H. H. Ehrich
,
et al.
Journal articles
istex
inserm-00410282v1
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Blockade of the kinin B1 receptor ameloriates glomerulonephritis.
Julie Klein
,
Julien Gonzalez
,
Stéphane Decramer
,
Flavio Bandin
,
Eric Neau
,
et al.
Journal articles
inserm-00506236v1
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The HNF1B score is a simple tool to select patients for HNF1B gene analysis
Stanislas Faguer
,
Nicolas Chassaing
,
Flavio Bandin
,
Cathie Prouheze
,
Arnaud Garnier
,
et al.
Journal articles
hal-03474737v1
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Hepatocyte nuclear factor‐1β shapes the energetic homeostasis of kidney tubule cells
Alexis Piedrafita
,
Stéphane Balayssac
,
Audrey Casemayou
,
Jean Sébastien Saulnier-Blache
,
Alexandre Lucas
,
et al.
Journal articles
inserm-03531997v1
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Thrombotic microangiopathy in a child with acute pancreatitis.
Emmanuel Mas
,
Christine Azéma
,
Anne Breton
,
Stéphane Decramer
,
Emmanuelle Fournié-Gardini
,
et al.
Journal articles
inserm-00409664v1
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The human urinary proteome reveals high similarity between kidney aging and chronic kidney disease.
Petra Zürbig
,
Stéphane Decramer
,
Mohammed Dakna
,
Justyna Jantos
,
David M. Good
,
et al.
Journal articles
inserm-00409938v1
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Congenital ureteropelvic junction obstruction: human disease and animal models.
Julie Klein
,
Julien Gonzalez
,
Mathieu Miravete
,
Cécile Caubet
,
Rana Chaaya
,
et al.
Journal articles
inserm-00550883v1
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Fetal Urinary Peptides to Predict Postnatal Outcome of Renal Disease in Fetuses with Posterior Urethral Valves (PUV).
Julie Klein
,
Chrystelle Lacroix
,
Cécile Caubet
,
Justyna Siwy
,
Petra Zürbig
,
et al.
Journal articles
inserm-00853060v1
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Systems biology combining human- and animal-data miRNA and mRNA data identifies new targets in ureteropelvic junction obstruction
Theofilos Papadopoulos
,
Audrey Casemayou
,
Eric Neau
,
Benjamin Breuil
,
Cécile Caubet
,
et al.
Journal articles
inserm-01480970v1
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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
Camille Fédou
,
Mylène Camus
,
Ophélie Lescat
,
Guylène Feuillet
,
Ilka Mueller
,
et al.
Journal articles
inserm-03268515v1
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Urinary proteome analysis identifies infants but not older children requiring pyeloplasty.
Jens Drube
,
Petra Zürbig
,
Eric Schiffer
,
Esther Lau
,
Benno Ure
,
et al.
Journal articles
istex
inserm-00505093v1
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Nephrin mutations can cause childhood-onset steroid-resistant nephrotic syndrome.
Aurélie Philippe
,
Fabien Nevo
,
Ernie L. Esquivel
,
Dalia Reklaityte
,
Olivier Gribouval
,
et al.
Journal articles
inserm-00409360v1
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Urinary proteome analysis at 5-year followup of patients with nonoperated ureteropelvic junction obstruction suggests ongoing kidney remodeling.
Flavio Bandin
,
Justyna Siwy
,
Benjamin Breuil
,
Harald Mischak
,
Jean-Loup Bascands
,
et al.
Journal articles
inserm-00726782v1
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Quality of life in children with severe forms of idiopathic nephrotic syndrome in stable remission—A cross‐sectional study
Aphaia Roussel
,
Jean-Daniel Delbet
,
Laurianne Micheland
,
Georges Deschênes
,
Stéphane Decramer
,
et al.
Journal articles
hal-02361199v1
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Defects in t6A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome
Christelle C. Arrondel
,
Sophia Missoury
,
Rozemarijn Snoek
,
Julie Patat
,
Giulia Menara
,
et al.
Journal articles
inserm-02322309v1
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Amniotic fluid peptides predict postnatal kidney survival in developmental kidney disease
Julie Klein
,
Bénédicte Buffin-Meyer
,
Franck Boizard
,
Nabila Moussaoui
,
Ophélie Lescat
,
et al.
Journal articles
inserm-03268524v1
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Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis
Hélène Louis-Dit-Picard
,
Ilektra Kouranti
,
Chloé Rafael
,
Irmine Loisel-Ferreira
,
Maria Chavez-Canales
,
et al.
Journal articles
hal-03832885v1
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Urine in clinical proteomics.
Stéphane Decramer
,
Anne Gonzalez de Peredo
,
Benjamin Breuil
,
Harald Mischak
,
Bernard Monsarrat
,
et al.
Journal articles
hal-00360866v1
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CKD and Its Risk Factors among Patients with Cystinuria
Caroline Prot-Bertoye
,
Saïd Lebbah
,
Michel Daudon
,
Isabelle Tostivint
,
Pierre Bataille
,
et al.
Journal articles
hal-02081201v1
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