List of works - Véronique Baudouin

Acute renal failure in a 3-year-old child as part of the drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome following hepatitis A.

scientific article

Age-Dependent Risk of Graft Failure in Young Kidney Transplant Recipients

scientific article published on August 2016

C3 nephritic factor associated with C3 glomerulopathy in children

scientific article published on 26 September 2013

Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant

scientific article published on 14 January 2009

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

scientific article published on 23 October 2017

Combination therapy of rituximab and mycophenolate mofetil in childhood lupus nephritis

scientific article published on 05 August 2017

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

scientific article published on 2 July 2015

Cryptosporidiosis in paediatric renal transplantation

scientific article published in November 2009

Cytomegalovirus infection can mimic genetic nephrotic syndrome: a case report

scientific article published on 22 September 2015

Effect of hydrochlorothiazide on urinary calcium excretion in dent disease: an uncontrolled trial

scientific article

Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

scientific article published on 10 March 2016

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

scientific article published on 11 August 2009

LMX1B mutations cause hereditary FSGS without extrarenal involvement

scientific article published on 16 May 2013

Literature review and case histories of Histoplasma capsulatum var. duboisii infections in HIV-infected patients

scientific article

Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations

scientific article

Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.

scientific article published on 11 June 2015

Observations of a large Dent disease cohort

scientific article published on 22 June 2016

Population pharmacokinetics and pharmacogenetics of once daily prolonged-release formulation of tacrolimus in pediatric and adolescent kidney transplant recipients

scientific article published on 17 June 2012

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

scientific article

Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

scientific article

Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome

scientific article

Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

scientific article

Therapy for acute rejection in pediatric organ transplant recipients

scientific article

Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two cases

scientific article

List of works by Véronique Baudouin

Acute renal failure in a 3-year-old child as part of the drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome following hepatitis A.

Age-Dependent Risk of Graft Failure in Young Kidney Transplant Recipients

C3 nephritic factor associated with C3 glomerulopathy in children

Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

Combination therapy of rituximab and mycophenolate mofetil in childhood lupus nephritis

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

Cryptosporidiosis in paediatric renal transplantation

Cytomegalovirus infection can mimic genetic nephrotic syndrome: a case report

Effect of hydrochlorothiazide on urinary calcium excretion in dent disease: an uncontrolled trial

Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences

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

LMX1B mutations cause hereditary FSGS without extrarenal involvement

Literature review and case histories of Histoplasma capsulatum var. duboisii infections in HIV-infected patients

Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations

Mutation Update of the CLCN5 Gene Responsible for Dent Disease 1.

Observations of a large Dent disease cohort

Population pharmacokinetics and pharmacogenetics of once daily prolonged-release formulation of tacrolimus in pediatric and adolescent kidney transplant recipients

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

Successful pre-transplant management of a patient with anti-factor H autoantibodies-associated haemolytic uraemic syndrome

Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

Therapy for acute rejection in pediatric organ transplant recipients

Varicella as a trigger of atypical haemolytic uraemic syndrome associated with complement dysfunction: two cases