Lista de obras - Chantal Loirat - Dominio Público Uruguay

Alternative complement pathway assessment in patients with atypical HUS.

artículo científico publicado en 2011

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

artículo científico publicado en 2004

Atypical hemolytic uremic syndrome

artículo científico publicado en 2011

Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome

artículo científico publicado en 2010

Complement and the atypical hemolytic uremic syndrome in children.

artículo científico publicado en 2008

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

artículo científico publicado en 2007

Enteric-coated mycophenolate sodium in de novo pediatric renal transplant patients

artículo científico publicado en 2008

Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome

artículo científico publicado en 2006

Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome

artículo científico publicado en 2010

HNF1beta/TCF2 mutations impair transactivation potential through altered co-regulator recruitment

artículo científico publicado en 2004

Hemolytic uremic syndrome recurrence after renal transplantation

artículo científico publicado en 2008

Hemolytic-uremic syndrome: what is the mechanism?

artículo científico publicado en 2008

Hereditary hemolytic uremic syndromes and thrombotic thrombocytopenic purpura

artículo científico publicado en 2006

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

Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome

artículo científico publicado en 2009

Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy

artículo científico publicado en 2008

In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys

artículo científico publicado en 2003

Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease

artículo científico publicado en 2009

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

artículo científico publicado en 2008

Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome

artículo científico publicado en 2010

Overall neutralization of complement factor H by autoantibodies in the acute phase of the autoimmune form of atypical hemolytic uremic syndrome

artículo científico publicado en 2012

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

artículo científico publicado en 2009

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

artículo científico publicado en 2013

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

artículo científico publicado en 2008

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

artículo científico publicado en 2009

Lista de obras de Chantal Loirat

Alternative complement pathway assessment in patients with atypical HUS.

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

Atypical hemolytic uremic syndrome

Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome

Complement and the atypical hemolytic uremic syndrome in children.

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

Enteric-coated mycophenolate sodium in de novo pediatric renal transplant patients

Genetic and functional analyses of membrane cofactor protein (CD46) mutations in atypical hemolytic uremic syndrome

Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome

HNF1beta/TCF2 mutations impair transactivation potential through altered co-regulator recruitment

Hemolytic uremic syndrome recurrence after renal transplantation

Hemolytic-uremic syndrome: what is the mechanism?

Hereditary hemolytic uremic syndromes and thrombotic thrombocytopenic purpura

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

Hyperfunctional C3 convertase leads to complement deposition on endothelial cells and contributes to atypical hemolytic uremic syndrome

Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy

In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys

Mutational analysis of CLC-5, cofilin and CLC-4 in patients with Dent's disease

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome

Overall neutralization of complement factor H by autoantibodies in the acute phase of the autoimmune form of atypical hemolytic uremic syndrome

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

Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome

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

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