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42

Zoubida Karim


Journal articles42 documents

  • Raêd Daher, Nicolas Ducrot, Thibaud Lefebvre, Sofia Zineeddine, Jérome Ausseil, et al.. Crosstalk between Acidosis and Iron Metabolism: Data from In Vivo Studies. Metabolites, 2022, 12 (2), pp.89. ⟨10.3390/metabo12020089⟩. ⟨inserm-03874980⟩
  • Maria Qatato, Michael Bonadonna, Gaël Palais, Alina Ertl, Gabriele Schmidt, et al.. IRE-dependent Regulation of Intestinal Dmt1 Prevails During Chronic Dietary Iron Deficiency but is Dispensable in Conditions of Acute Erythropoietic Stress. HemaSphere, 2022, 6 (3), pp.e693. ⟨10.1097/HS9.0000000000000693⟩. ⟨inserm-03874988⟩
  • Meunier Mathieu, Chloé Friedrich, Nicolas Ducrot, Johanna Zannoni, Tondeur Sylvie, et al.. Luspatercept (RAP-536) modulates oxidative stress without affecting mutation burden in myelodysplastic syndromes. Annals of Hematology, 2022, 101 (12), pp.2633-2643. ⟨10.1007/s00277-022-04993-7⟩. ⟨hal-03876188⟩
  • Meunier Mathieu, Chloé Friedrich, Nicolas Ducrot, Johanna Zannoni, Tondeur Sylvie, et al.. Luspatercept (RAP-536) modulates oxidative stress without affecting mutation burden in myelodysplastic syndromes. Annals of Hematology, 2022, 101 (12), pp.2633-2643. ⟨10.1007/s00277-022-04993-7⟩. ⟨inserm-03874959⟩
  • Maxime Touzot, Thibaud Lefebvre, Catherine Maheas, Katell Peoc'H, Pablo Ureña-Torres, et al.. Kinetics of serum hepcidin and interleukin-6 levels following COVID-19 infection in hemodialysis patients. Clinical Kidney Journal, 2022, 15 (3), pp.582-583. ⟨10.1093/ckj/sfab254⟩. ⟨hal-03764736⟩
  • Gérald Le Gac, Virginie Scotet, Isabelle Gourlaouen, Carine L'Hostis, Marie-Christine Merour, et al.. Prevalence of HFE-related haemochromatosis and secondary causes of hyperferritinaemia and their association with iron overload in 1059 French patients treated by venesection. Alimentary Pharmacology and Therapeuthics, 2022, 55 (8), pp.1016-1027. ⟨10.1111/apt.16775⟩. ⟨hal-03592561⟩
  • Thibaud Lefebvre, Muriel Coupaye, Marina Esposito-Farèse, Nathalie Gault, Neila Talbi, et al.. Hepcidin and Iron Deficiency in Women One Year after Sleeve Gastrectomy: A Prospective Cohort Study. Nutrients, MDPI, 2021, 13 (8), pp.2516. ⟨10.3390/nu13082516⟩. ⟨hal-03448937⟩
  • Colin P Farrell, Gaël Nicolas, Robert Desnick, Charles J Parker, Jerome Lamoril, et al.. ABCB6 Polymorphisms are not Overly Represented in Patients with Porphyria. Blood Advances, The American Society of Hematology, 2021, ⟨10.1182/bloodadvances.2021005484⟩. ⟨hal-03483658⟩
  • Colin Farrell, Gaël Nicolas, Robert Desnick, Charles Parker, Jerome Lamoril, et al.. ABCB6 Polymorphisms are not Overly Represented in Patients with Porphyria Tracking no: ADV-2021-005484R1. Blood Advances, The American Society of Hematology, In press, ⟨10.1182/bloodadvances.2021005484⟩. ⟨hal-03450020⟩
  • Jean-Marc Blouin, Cécile Ged, Magalie Lalanne, Isabelle Lamrissi-Garcia, Fanny Morice-Picard, et al.. Iron chelation rescues hemolytic anemia and skin photosensitivity in congenital erythropoietic porphyria. Blood, American Society of Hematology, 2020, 136 (21), pp.2457-2468. ⟨10.1182/blood.2020006037⟩. ⟨hal-03045807⟩
  • Elisabeth Tybl, Hiromi Gunshin, Sanjay Gupta, Tomasa Barrientos, Michael Bonadonna, et al.. Control of Systemic Iron Homeostasis by the 3’ Iron-Responsive Element of Divalent Metal Transporter 1 in Mice. HemaSphere, Lippincott, Williams & Wilkins, 2020, 4 (5), pp.e459. ⟨10.1097/HS9.0000000000000459⟩. ⟨hal-03043109⟩
  • Maxime Touzot, Thibaud Lefebvre, Catherine Maheas, Christophe Ridel, Hervé Puy, et al.. A hepcidin‐based approach for iron therapy in hemodialysis patients: A pilot study. Hemodialysis International, Wiley, 2020, 24 (2), pp.188-194. ⟨10.1111/hdi.12823⟩. ⟨hal-03046316⟩
  • Sabrina Bondu, Anne-Sophie Alary, Carine Lefevre, Alexandre Houy, Grace Jung, et al.. A variant erythroferrone disrupts iron homeostasis in SF3B1-mutated myelodysplastic syndrome. Science Translational Medicine, 2019, 11 (500), pp.eaav5467. ⟨10.1126/scitranslmed.aav5467⟩. ⟨inserm-02449216⟩
  • Raêd Daher, Thibaud Lefebvre, Hervé Puy, Zoubida Karim. Extrahepatic hepcidin production: The intriguing outcomes of recent years. World Journal of Clinical Cases, Baishideng Publishing Group 2019, 7 (15), pp.1926-1936. ⟨10.12998/wjcc.v7.i15.1926⟩. ⟨hal-03046342⟩
  • Thibaud Lefebvre, Sarah Millot, Emmanuel Richard, Jean-Marc Blouin, Magalie Lalanne, et al.. Genetic background influences hepcidin response to iron imbalance in a mouse model of hemolytic anemia (Congenital erythropoietic porphyria). Biochemical and Biophysical Research Communications, Elsevier, 2019, 520 (2), pp.297-303. ⟨10.1016/j.bbrc.2019.09.141⟩. ⟨hal-03046353⟩
  • Raed Daher, Abdellah Mansouri, Alain Martelli, Sophie Bayart, Hana Manceau, et al.. GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemia. Molecular Genetics and Metabolism, Elsevier, 2019, ⟨10.1016/j.ymgme.2018.12.012⟩. ⟨hal-02351427⟩
  • Sarah Rio, Marc Gastou, Narjesse Karboul, Raphaёl Derman, Thunwarat Suriyun, et al.. Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1. Blood, 2019, 133 (12), pp.1358-1370. ⟨10.1182/blood-2018-09-875674⟩. ⟨hal-02339695⟩
  • Camille Petillon, Rudolf Hergesheimer, Hervé Puy, Philippe Corcia, Patrick Vourc'H, et al.. The Relevancy of Data Regarding the Metabolism of Iron to Our Understanding of Deregulated Mechanisms in ALS; Hypotheses and Pitfalls. Frontiers in Neuroscience, Frontiers, 2019, 12, pp.1031. ⟨10.3389/fnins.2018.01031⟩. ⟨hal-02351424⟩
  • Arienne Mirmiran, Caroline Schmitt, Thibaud Lefebvre, Hana Manceau, Raed Daher, et al.. Erythroid-Progenitor-Targeted Gene Therapy Using Bifunctional TFR1 Ligand-Peptides in Human Erythropoietic Protoporphyria. American Journal of Human Genetics, Elsevier (Cell Press), 2019, 104 (2), pp.341-347. ⟨10.1016/j.ajhg.2018.12.021⟩. ⟨hal-02328937⟩
  • Raed Daher, Thibaud Lefebvre, Hervé Puy, Zoubida Karim. Extrahepatic hepcidin production: The intriguing outcomes of recent years. World Journal of Clinical Cases, Baishideng Publishing Group 2019, 7 (15), pp.1926-1936. ⟨10.12998/wjcc.v7.i15.1926⟩. ⟨hal-02350928⟩
  • Zoubida Karim. Genetic background influences hepcidin response to iron imbalance in a mouse model of hemolytic anemia (Congenital erythropoietic porphyria). Biochemical and Biophysical Research Communications, Elsevier, In press, ⟨10.1016/j.bbrc.2019.09.141⟩. ⟨hal-02350852⟩
  • Sophie Park, Olivier Kosmider, Fréderic Maloisel, Bernard Drénou, Nicolas Chapuis, et al.. Dyserythropoiesis evaluated by the RED score and hepcidin:ferritin ratio predicts response to erythropoietin in lower-risk myelodysplastic syndromes. Haematologica, 2019, 104 (3), pp.497-504. ⟨10.3324/haematol.2018.203158⟩. ⟨hal-02351432⟩
  • Katell Peoc'H, Gaël Nicolas, Caroline Schmitt, Arienne Mirmiran, Raed Daher, et al.. Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias. Molecular Genetics and Metabolism, Elsevier, 2019, ⟨10.1016/j.ymgme.2019.01.015⟩. ⟨hal-02351175⟩
  • Maxime Touzot, Thibaud Lefebvre, Arthur Roux, Catherine Maheas, Christophe Ridel, et al.. Functional erythropoietin‐hepcidin axis in recombinant human erythropoietin independent haemodialysis patients. Nephrology, 2019, 24 (7), pp.751-757. ⟨10.1111/nep.13485⟩. ⟨hal-02351435⟩
  • Katell Peoc'H, Gaël Nicolas, Caroline Schmitt, Arienne Mirmiran, Raed Daher, et al.. Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias. Molecular Genetics and Metabolism, Elsevier, 2019, ⟨10.1016/j.ymgme.2019.01.015⟩. ⟨inserm-02075450⟩
  • Caroline Schmitt, Hugo Lenglet, Angèle Yu, Constance Delaby, Arndt Benecke, et al.. Recurrent attacks of acute hepatic porphyria: major role of the chronic inflammatory response in the liver. Journal of Internal Medicine, Wiley, 2018, 284 (1), pp.78-91. ⟨10.1111/joim.12750⟩. ⟨hal-02503870⟩
  • Katell Peoc'H, Hana Manceau, Zoubida Karim, Staffan Wahlin, Laurent Gouya, et al.. Hepatocellular carcinoma in acute hepatic porphyrias: A Damocles Sword. Molecular Genetics and Metabolism, Elsevier, 2018, ⟨10.1016/j.ymgme.2018.10.001⟩. ⟨hal-02351428⟩
  • Jeremy Rouillon, Thibaud Lefebvre, Jérôme Denard, Vincent Puy, Raed Daher, et al.. High urinary ferritin reflects myoglobin iron evacuation in DMD patients. Neuromuscular Disorders, Elsevier, 2018, 28 (7), pp.564-571. ⟨10.1016/j.nmd.2018.03.008⟩. ⟨hal-02351437⟩
  • Thibaud Lefebvre, Niloofar Reihani, Raed Daher, Thierry Billette de Villemeur, Nadia Belmatoug, et al.. Involvement of hepcidin in iron metabolism dysregulation in Gaucher disease. Haematologica, Ferrata Storti Foundation, 2018, 103 (4), pp.587-596. ⟨10.3324/haematol.2017.177816⟩. ⟨hal-01762401⟩
  • Nicolas Pallet, Alexandre Karras, Eric Thervet, Laurent Gouya, Zoubida Karim, et al.. Porphyria and kidney diseases. Clinical Kidney Journal, Oxford University Press, 2018, 11 (2), pp.191-197. ⟨10.1093/ckj/sfx146⟩. ⟨hal-02351440⟩
  • Vincent Puy, Walaa Darwiche, Stephanie Trudel, Cathy Gomila, Christelle Lony, et al.. Predominant role of microglia in brain iron retention in Sanfilippo syndrome, a pediatric neurodegenerative disease. Glia, Wiley, 2018, 66 (8), pp.1709-1723. ⟨10.1002/glia.23335⟩. ⟨hal-02351442⟩
  • Hugo Lenglet, Caroline Schmitt, Thomas Grange, Hana Manceau, Narjesse Karboul, et al.. From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria. Human Molecular Genetics, Oxford University Press (OUP), 2018, 27 (7), pp.1164-1173. ⟨10.1093/hmg/ddy030⟩. ⟨hal-02351445⟩
  • Mariane de Montalembert, Jean-Antoine Ribeil, Valentine Brousse, Agnès Guerci-Bresler, Aspasia Stamatoullas, et al.. Cardiac iron overload in chronically transfused patients with thalassemia, sickle cell anemia, or myelodysplastic syndrome. PLoS ONE, Public Library of Science, 2017, 12 (3), pp.e0172147. ⟨10.1371/journal.pone.0172147⟩. ⟨hal-02377929⟩
  • Yvette Yien, Sarah Ducamp, Lisa van Der Vorm, Julia Kardon, Hana Manceau, et al.. Mutation in human CLPX elevates levels of δ- aminolevulinate synthase and protoporphyrin IX to promote erythropoietic protoporphyria. Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2017, 114 (38), pp.E8045-E8052. ⟨10.1073/pnas.1700632114⟩. ⟨inserm-02075468⟩
  • Raed Daher, Hana Manceau, Zoubida Karim. Iron metabolism and the role of the iron-regulating hormone hepcidin in health and disease. La Presse Médicale, Elsevier Masson, 2017, 46 (12), pp.e272-e278. ⟨10.1016/j.lpm.2017.10.006⟩. ⟨hal-02351459⟩
  • Vincent Puy, Pierre-Edouard Bodet, Camille Rottier, Rémi Delaunay, Cathy Gomila, et al.. Corrigendum to “Alteration of cerebral iron metabolism in Sanfilippo syndrome” [Mol. Genet. Metab. 117 2, February 2016, p. S97]. Molecular Genetics and Metabolism, Elsevier, 2016, 118 (1), pp.64. ⟨10.1016/j.ymgme.2016.03.005⟩. ⟨hal-02065247⟩
  • Jean-Christophe Deschemin, Marie-Louise M.-L. Noordine, Aude Remot, Alexandra Willemetz, Clément Afif, et al.. The microbiota shifts the iron sensing of intestinal cells. FASEB Journal, 2016, 30 (1), pp.252-261. ⟨10.1096/fj.15-276840⟩. ⟨hal-02632319⟩
  • Raed Daher, Caroline Kannengiesser, Dounia Houamel, Thibaud Lefebvre, Edouard Bardou-Jacquet, et al.. Heterozygous Mutations in BMP6 Pro-peptide Lead to Inappropriate Hepcidin Synthesis and Moderate Iron Overload in Humans. Gastroenterology, Elsevier, 2016, 150 (3), pp.672-683. ⟨10.1053/j.gastro.2015.10.049⟩. ⟨hal-01231430⟩
  • Nicolas Pallet, Iadh Mami, Caroline Schmitt, Zoubida Karim, Arnaud François, et al.. High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyria. Kidney International, Nature Publishing Group, 2015, 88 (2), pp.386-395. ⟨10.1038/ki.2015.97⟩. ⟨hal-02317945⟩
  • Chadi Homedan, Caroline Schmitt, Jihane Laafi, Naïg Gueguen, Valérie Desquiret-Dumas, et al.. Mitochondrial energetic defects in muscle and brain of a Hmbs-/- mouse model of acute intermittent porphyria. Human molecular genetics online, 2015, 24 (17), pp.5015-23. ⟨10.1093/hmg/ddv222⟩. ⟨hal-02056592⟩
  • Chadi Homedan, Jihane Laafi, Caroline Schmitt, Naïg Gueguen, Thibaud Lefebvre, et al.. Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse model. International Journal of Biochemistry and Cell Biology, Elsevier, 2014, 51, pp.93-101. ⟨10.1016/j.biocel.2014.03.032⟩. ⟨hal-03328708⟩
  • Saïd Lyoumi, Marie Abitbol, Dominique Rainteau, Zoubida Karim, Florence Bernex, et al.. Protoporphyrin retention in hepatocytes and kupffer cells prevents sclerosing cholangitis in erythropoietic protoporphyria mouse model.. Gastroenterology, Elsevier, 2011, 141 ((4)), pp.1509-1519.e3. ⟨10.1053/j.gastro.2011.06.078⟩. ⟨hal-00631510⟩