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EMBO Molecular Medicine|January 31, 2024
Infected erythrocytes and plasma proteomics reveal a specific protein signature of severe malariaJeremy Fraering, Virginie Salnot, Emilie-Fleur Gautier, et al.
European Journal of Gastroenterology & Hepatology|January 3, 2020
Biological response under treatment and prognostic value of protein induced by vitamin K absence or antagonist-II in a French cohort of patients with hepatocellular carcinomaAudrey Payancé, Marco Dioguardi Burgio, Katell Peoc'h, et al.
Critical Care Explorations|February 9, 2024
Association of Sepsis With Neurologic Outcomes of Adult Patients Treated With Venoarterial Extracorporeal Membrane OxygnenationChloé Tridon, Delphine Bachelet, Majda El Baied, et al.
Blood Cells, Molecules & Diseases|August 4, 2017
Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutationMarie-Amelyne Le Rouzic, Cyrielle Fouquet, Thierry Leblanc, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 7, 2023
Evaluation of iron metabolism in hospitalized COVID-19 patientsThibaud Lefebvre, Anne Boutten, Célia Raulet-Bussian, et al.
American Journal of Human Genetics|February 5, 2019
Erythroid-Progenitor-Targeted Gene Therapy Using Bifunctional TFR1 Ligand-Peptides in Human Erythropoietic ProtoporphyriaArienne Mirmiran, Caroline Schmitt, Thibaud Lefebvre, et al.
Human Molecular Genetics|January 24, 2018
From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyriaHugo Lenglet, Caroline Schmitt, Thomas Grange, et al.
Molecular Genetics and Metabolism|January 21, 2022
Givosiran in acute intermittent porphyria: A personalized medicine approachAntoine Poli, Caroline Schmitt, Boualem Moulouel, et al.
American Journal of Human Genetics|April 1, 2014
Antisense oligonucleotide-based therapy in human erythropoietic protoporphyriaVincent Oustric, Hana Manceau, Sarah Ducamp, et al.
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