Marie‐Alice Macher

The Clinical Spectrum and Therapeutic Management of Hypocomplementemic Urticarial Vasculitis: Data From a French Nationwide Study of Fifty‐Seven Patients

M. Jachiet, B. Flageul, Alban Deroux et al. · Arthritis & Rheumatology · 2014 · 172 citations

Improving Mutation Screening in Familial Hematuric Nephropathies through Next Generation Sequencing

Vincent Morinière, Karin Dahan, Pascale Hilbert et al. · Journal of the American Society of Nephrology · 2014 · 166 citations · Full text

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

Karine Brochard, Olivia Boyer, Anne Blanchard et al. · Nephrology Dialysis Transplantation · 2008 · 165 citations

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

Jérôme Harambat, Sonia Fargue, Cécile Acquaviva et al. · Kidney International · 2009 · 151 citations · Full text

Allelic Variant, Primary Hyperoxaluria, Genetic Disorder +10

Genetic Investigation of Autosomal Recessive Distal Renal Tubular Acidosis

Rosa Vargas‐Poussou, Pascal Houillier, Nelly Le Pottier et al. · Journal of the American Society of Nephrology · 2006 · 137 citations

Biology, Subunits B1, Genetic Disorder +13