Philippe Eckart

Neurological disorders in pediatric emergency department: From consultation to follow-up of first epileptic seizures.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: July 29, 2024

Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions.

Journal: Kidney international reports

Published: February 13, 2024

Prescription practice and yield of chest radiography in the management of children presenting to the French pediatric emergency department with non-traumatic chest pain.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: September 20, 2023

A very uncommon cause of acute kidney injury in infancy.

Journal: Kidney international

Published: December 28, 2020

Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trial.

Journal: BMJ open

Published: September 24, 2020

Bi-allelic mutations in renin-angiotensin system genes, associated with renal tubular dysgenesis, can also present as a progressive chronic kidney disease.

Journal: Pediatric nephrology (Berlin, Germany)

Published: January 15, 2020

Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia.

Journal: European journal of medical genetics

Published: April 09, 2018

School level of children carrying a HNF1B variant or a deletion.

Journal: European journal of human genetics : EJHG

Published: December 18, 2017

Eculizumab treatment in severe pediatric STEC-HUS: a multicenter retrospective study.

Journal: Pediatric nephrology (Berlin, Germany)

Published: June 27, 2017

Profile of bacterial resistance in pediatric urinary tract infections in 2014

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: February 18, 2016

CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait.

Journal: The Journal of clinical endocrinology and metabolism

Published: July 28, 2015

NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.

Journal: Human mutation

Published: August 12, 2013

Neurological disorders in pediatric emergency department: From consultation to follow-up of first epileptic seizures.

Neurological disorders in pediatric emergency department: From consultation to follow-up of first epileptic seizures.

Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions.

Renal and Extrarenal Phenotypes in Patients With HNF1B Variants and Chromosome 17q12 Microdeletions.

Prescription practice and yield of chest radiography in the management of children presenting to the French pediatric emergency department with non-traumatic chest pain.

Prescription practice and yield of chest radiography in the management of children presenting to the French pediatric emergency department with non-traumatic chest pain.

A very uncommon cause of acute kidney injury in infancy.

A very uncommon cause of acute kidney injury in infancy.

Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trial.

Efficacy and safety of intravenous immunoglobulin with rituximab versus rituximab alone in childhood-onset steroid-dependent and frequently relapsing nephrotic syndrome: protocol for a multicentre randomised controlled trial.

Bi-allelic mutations in renin-angiotensin system genes, associated with renal tubular dysgenesis, can also present as a progressive chronic kidney disease.

Bi-allelic mutations in renin-angiotensin system genes, associated with renal tubular dysgenesis, can also present as a progressive chronic kidney disease.

Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia.

Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia.

School level of children carrying a HNF1B variant or a deletion.

School level of children carrying a HNF1B variant or a deletion.

Eculizumab treatment in severe pediatric STEC-HUS: a multicenter retrospective study.

Eculizumab treatment in severe pediatric STEC-HUS: a multicenter retrospective study.

Profile of bacterial resistance in pediatric urinary tract infections in 2014

Profile of bacterial resistance in pediatric urinary tract infections in 2014

CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait.

CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait.

NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.

NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum.

Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia.

Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia.