Marie-lucile Figueres
Paris, France
Last Updated: 09/26/2026
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Found 12 publications
Characterization of Renal Injury and Inflammation in an Experimental Model of Intravascular Hemolysis.
Journal: Frontiers in immunology
Published: October 04, 2017
Intravascular hemolysis activates complement via cell-free heme and heme-loaded microvesicles.
Journal: JCI insight
Published: August 18, 2017
Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 15, 2017
Loss of tubular creatinine secretion as the only sign of tubular proximal cell dysfunction in light chain proximal tubulopathy: A case report.
Journal: Medicine
Published: July 02, 2016
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations.
Journal: Journal of medical genetics
Published: May 11, 2016
Claudin-16 Deficiency Impairs Tight Junction Function in Ameloblasts, Leading to Abnormal Enamel Formation.
Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
Published: May 15, 2015
Diagnostic value of IgG subtypes in membranous nephropathy: A case report
Journal: Nephrologie & therapeutique
Published: October 14, 2014
Kidney function and influence of sunlight exposure in patients with impaired 24-hydroxylation of vitamin D due to CYP24A1 mutations.
Journal: American journal of kidney diseases : the official journal of the National Kidney Foundation
Published: December 04, 2013
Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.
Journal: Nephron. Physiology
Published: February 20, 2013
Aspergillus arthritis and organ transplantation.
Journal: Clinical kidney journal
Published: December 07, 2011
Showing 1-12 of 12
Last Updated: 09/26/2026