List of works - Marie-Alice Macher

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

scientific article published on August 2016

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

scientific article

Are there good reasons for inequalities in access to renal transplantation in children?

scientific article published on 23 November 2014

C3 nephritic factor associated with C3 glomerulopathy in children

scientific article published on 26 September 2013

Cinacalcet in hyperparathyroidism management after pediatric renal transplantation

scientific article published on 22 January 2016

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

scientific article

Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1.

scientific article

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

Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome

scientific article published on 16 December 2009

High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations

scientific article

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

scientific article

Improving mutation screening in familial hematuric nephropathies through next generation sequencing

scientific article

Infection-related hospitalizations after kidney transplantation in children: incidence, risk factors, and cost

scientific article

Long-term outcome of prenatally detected posterior urethral valves: single center study of 65 cases managed by primary valve ablation

scientific article published on 19 November 2007

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

scientific article published on 11 June 2015

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

scientific article

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

scientific article

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

scientific article

The clinical spectrum and therapeutic management of hypocomplementemic urticarial vasculitis: data from a French nationwide study of fifty-seven patients

scientific article

List of works by Marie-Alice Macher

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

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome

Are there good reasons for inequalities in access to renal transplantation in children?

C3 nephritic factor associated with C3 glomerulopathy in children

Cinacalcet in hyperparathyroidism management after pediatric renal transplantation

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

Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1.

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

Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome

High NPHP1 and NPHP6 mutation rate in patients with Joubert syndrome and nephronophthisis: potential epistatic effect of NPHP6 and AHI1 mutations in patients with NPHP1 mutations

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

Improving mutation screening in familial hematuric nephropathies through next generation sequencing

Infection-related hospitalizations after kidney transplantation in children: incidence, risk factors, and cost

Long-term outcome of prenatally detected posterior urethral valves: single center study of 65 cases managed by primary valve ablation

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

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

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

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

The clinical spectrum and therapeutic management of hypocomplementemic urticarial vasculitis: data from a French nationwide study of fifty-seven patients