Lista de obras - Véronique Baudouin - Dominio Público Uruguay

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.

artículo científico publicado en 2007

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

artículo científico publicado en 2016

C3 nephritic factor associated with C3 glomerulopathy in children

artículo científico publicado en 2013

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

artículo científico publicado en 2009

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

artículo científico publicado en 2017

Combination therapy of rituximab and mycophenolate mofetil in childhood lupus nephritis

artículo científico

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

artículo científico publicado en 2015

Cryptosporidiosis in paediatric renal transplantation

artículo científico publicado en 2009

Cytomegalovirus infection can mimic genetic nephrotic syndrome: a case report

artículo científico publicado en 2015

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

artículo científico publicado en 2008

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

artículo científico publicado en 2016

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

artículo científico publicado en 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

artículo científico publicado en 2007

Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations

artículo científico publicado en 2012

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

artículo científico

Observations of a large Dent disease cohort

artículo científico publicado en 2016

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

artículo científico publicado en 2012

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

artículo científico publicado en 2013

Spondyloenchondrodysplasia Due to Mutations in ACP5: A Comprehensive Survey

artículo científico publicado en 2016

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

artículo científico publicado en 2008

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

artículo científico publicado en 2011

Therapy for acute rejection in pediatric organ transplant recipients

artículo científico publicado en 2003

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

artículo científico publicado en 2009

Lista de obras de 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