Lista de obras - Georges Deschênes - Dominio Público Uruguay

A randomized controlled crossover trial with delayed-release cysteamine bitartrate in nephropathic cystinosis: effectiveness on white blood cell cystine levels and comparison of safety

artículo científico publicado en 2012

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

Antenatal membranous glomerulonephritis with vascular injury induced by anti-neutral endopeptidase antibodies: toward new concepts in the pathogenesis of glomerular diseases

artículo científico publicado en 2003

Arterial hypertension and ovarian tumour in a girl: what is the link?

artículo científico publicado en 2004

Blockade of alternative complement pathway in dense deposit disease

artículo científico publicado en 2014

Cinacalcet in hyperparathyroidism management after pediatric renal transplantation

artículo científico publicado en 2016

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

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

Controversies and research agenda in nephropathic cystinosis: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference

artículo científico publicado en 2016

Cytomegalovirus infection can mimic genetic nephrotic syndrome: a case report

artículo científico publicado en 2015

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome

artículo científico publicado en 2007

Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease

artículo científico publicado en 2015

Early-childhood membranous nephropathy due to cationic bovine serum albumin

artículo científico publicado en 2011

Exposure to maternal diabetes induces salt-sensitive hypertension and impairs renal function in adult rat offspring

artículo científico publicado en 2008

Fetal urine biochemistry in antenatal Bartter syndrome: a case report

scientific article published on 08 August 2016

Fulminant viral myocarditis after rituximab therapy in pediatric nephrotic syndrome

artículo científico publicado en 2013

Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults

artículo científico publicado en 2013

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

artículo científico publicado en 2009

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

artículo científico publicado en 2004

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy

artículo científico publicado en 2011

Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

artículo científico publicado en 2016

Inhibitory ITAM signaling by Fc alpha RI-FcR gamma chain controls multiple activating responses and prevents renal inflammation

artículo científico publicado en 2008

Intracellular Na+ controls cell surface expression of Na,K-ATPase via a cAMP-independent PKA pathway in mammalian kidney collecting duct cells

artículo científico publicado en 2003

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation

artículo científico publicado en 2005

Mechanism of control of Na,K-ATPase in principal cells of the mammalian collecting duct

artículo científico publicado en 2003

Molecular mechanism of edema formation in nephrotic syndrome: therapeutic implications

artículo científico publicado en 2007

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

artículo científico

Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulation

artículo científico publicado en 2010

Observations of a large Dent disease cohort

artículo científico publicado en 2016

Ocular involvement in hemolytic uremic syndrome due to factor H deficiency--are there therapeutic consequences?

artículo científico publicado en 2007

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome

artículo científico publicado en 2009

Physiopathology of idiopathic nephrotic syndrome: lessons from glucocorticoids and epigenetic perspectives

scientific article published on 28 June 2011

Plasma therapy in von Willebrand factor protease deficiency

artículo científico publicado en 2002

Population pharmacokinetics and pharmacodynamics of cysteamine in nephropathic cystinosis patients

artículo científico publicado en 2011

Population pharmacokinetics and pharmacogenetics of mycophenolic acid following administration of mycophenolate mofetil in de novo pediatric renal-transplant patients

artículo científico publicado en 2010

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

artículo científico publicado en 2012

Prevalence of herpesviruses at onset of idiopathic nephrotic syndrome

artículo científico publicado en 2014

Primary molecular disorders and secondary biological adaptations in bartter syndrome

artículo científico

Quality of life is improved and kidney function preserved in patients with nephropathic cystinosis treated for 2 years with delayed-release cysteamine bitartrate

artículo científico publicado en 2014

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

artículo científico publicado en 2013

Secondary failure of plasma therapy in factor H deficiency

artículo científico publicado en 2006

Tacrolimus nephrotoxicity: beware of the association of diarrhea, drug interaction and pharmacogenetics

artículo científico publicado en 2010

Lista de obras de Georges Deschênes

A randomized controlled crossover trial with delayed-release cysteamine bitartrate in nephropathic cystinosis: effectiveness on white blood cell cystine levels and comparison of safety

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.

Antenatal membranous glomerulonephritis with vascular injury induced by anti-neutral endopeptidase antibodies: toward new concepts in the pathogenesis of glomerular diseases

Arterial hypertension and ovarian tumour in a girl: what is the link?

Blockade of alternative complement pathway in dense deposit disease

Cinacalcet in hyperparathyroidism management after pediatric renal transplantation

Clinical and genetic heterogeneity in familial steroid-sensitive nephrotic syndrome

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

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

Combination therapy of rituximab and mycophenolate mofetil in childhood lupus nephritis

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

Controversies and research agenda in nephropathic cystinosis: conclusions from a "Kidney Disease: Improving Global Outcomes" (KDIGO) Controversies Conference

Cytomegalovirus infection can mimic genetic nephrotic syndrome: a case report

Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome

Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent disease

Early-childhood membranous nephropathy due to cationic bovine serum albumin

Exposure to maternal diabetes induces salt-sensitive hypertension and impairs renal function in adult rat offspring

Fetal urine biochemistry in antenatal Bartter syndrome: a case report

Fulminant viral myocarditis after rituximab therapy in pediatric nephrotic syndrome

Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults

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

Heterozygous and homozygous factor h deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy

Increased Wnt and Notch signaling: a clue to the renal disease in Schimke immuno-osseous dysplasia?

Inhibitory ITAM signaling by Fc alpha RI-FcR gamma chain controls multiple activating responses and prevents renal inflammation

Intracellular Na+ controls cell surface expression of Na,K-ATPase via a cAMP-independent PKA pathway in mammalian kidney collecting duct cells

Late-onset thrombocytic microangiopathy caused by cblC disease: association with a factor H mutation

Mechanism of control of Na,K-ATPase in principal cells of the mammalian collecting duct

Molecular mechanism of edema formation in nephrotic syndrome: therapeutic implications

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

Non-atheromatous arterial stenoses in atypical haemolytic uraemic syndrome associated with complement dysregulation

Observations of a large Dent disease cohort

Ocular involvement in hemolytic uremic syndrome due to factor H deficiency--are there therapeutic consequences?

Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome

Physiopathology of idiopathic nephrotic syndrome: lessons from glucocorticoids and epigenetic perspectives

Plasma therapy in von Willebrand factor protease deficiency

Population pharmacokinetics and pharmacodynamics of cysteamine in nephropathic cystinosis patients

Population pharmacokinetics and pharmacogenetics of mycophenolic acid following administration of mycophenolate mofetil in de novo pediatric renal-transplant patients

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

Prevalence of herpesviruses at onset of idiopathic nephrotic syndrome

Primary molecular disorders and secondary biological adaptations in bartter syndrome

Quality of life is improved and kidney function preserved in patients with nephropathic cystinosis treated for 2 years with delayed-release cysteamine bitartrate

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

Secondary failure of plasma therapy in factor H deficiency

Tacrolimus nephrotoxicity: beware of the association of diarrhea, drug interaction and pharmacogenetics