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Medrxiv : the Preprint Server for Health Sciences|January 20, 2025
The ratio of plasma pTau217 to Aβ42 outperforms individual measurements in detecting brain amyloidosisSylvain Lehmann, Audrey Gabelle, Marie Duchiron, et al.
Clinical Chemistry and Laboratory Medicine|March 18, 2015
LC-MS/MS method for hepcidin-25 measurement in human and mouse serum: clinical and research implications in iron disordersThibaud Lefebvre, Nathalie Dessendier, Dounia Houamel, et al.
Human Mutation|January 6, 2006
Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolismFrancesca Ferrari, Barbara Foglieni, Paolo Arosio, et al.
Blood|September 17, 2010
Erythropoietin stimulates spleen BMP4-dependent stress erythropoiesis and partially corrects anemia in a mouse model of generalized inflammationSarah Millot, Valérie Andrieu, Philippe Letteron, et al.
Neurology|April 14, 2026
Influence of Decreased Kidney Function on Plasma Biomarkers of Neurodegenerative Disorders in Routine Care: Confirmation of the Interest of RatiosEtienne Mondésert, Jean-Paul Cristol, Anne-Sophie Bargnoux, et al.
Frontiers in Aging Neuroscience|November 17, 2022
Neurofilaments contribution in clinic: state of the artConstance Delaby, Olivier Bousiges, Damien Bouvier, et al.
Alzheimer'S Research & Therapy|June 3, 2015
Cerebrospinal fluid amyloid-β 42/40 ratio in clinical setting of memory centers: a multicentric studyJulien Dumurgier, Susanna Schraen, Audrey Gabelle, et al.
Annales De Biologie Clinique|December 1, 2022
Neurofilaments: a key new biomarker for clinicians. Part 1: Importance of neurofilaments in the management of neurodegenerative diseasesConstance Delaby, Olivier Bousiges, Damien Bouvier, et al.
Annales De Biologie Clinique|December 1, 2022
Neurofilaments: a key new biomarker for clinicians. Part 2: Neurofilaments, an asset beyond neurodegenerative diseasesConstance Delaby, Olivier Bousiges, Damien Bouvier, et al.
Blood|October 28, 2011
A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 geneBernard Grandchamp, Gilles Hetet, Caroline Kannengiesser, et al.
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