Dr. Alexandra Cambier’s Laboratory for the Improvement of Care and Diagnosis of Pediatric Glomerular Kidney Diseases.
News
The inauguration of the Centre of Expertise in Complement-Mediated Rare Diseases at CHU Sainte-Justine marks a major step forward in advancing the understanding, diagnosis, and treatment of these conditions through a unique translational research infrastructure in Canada. This centre will enable the development of local diagnostic tools, the centralization of specialized analyses, and the strengthening of international collaboration—ultimately improving access to care and enhancing patients’ quality of life.
Our projects
Through our work, we strive to improve the state of diagnosis and management of IgA Nephropathy in children by understanding the fundamental role of CD89 and collagen variants.
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Our research
Clinical and pathophysiological studies
Search for specific immune biomarkers for diagnosis and prognosis
Research into genetic predispositions
Research into specific treatments, implementation of randomized controlled trials with innovative molecules
Our team
Each Néphronté(e) strengthens the range of expertise, techniques, and knowledge available to the laboratory. With collaborators from around the world, we benefit from a rich and dynamic culture that enhances our work.
Meet our team
Our lab
Located at Sainte-Justine University Hospital, the laboratory aims to be a hub of expertise, techniques, and knowledge available to all. A true place for exchange, its proximity to the hospital allows us to integrate our projects with strong translational research.
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