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Kidney International|April 2, 2015
High prevalence of and potential mechanisms for chronic kidney disease in patients with acute intermittent porphyriaNicolas Pallet, Iadh Mami, Caroline Schmitt, et al.
The International Journal of Biochemistry & Cell Biology|April 15, 2014
Acute intermittent porphyria causes hepatic mitochondrial energetic failure in a mouse modelChadi Homedan, Jihane Laafi, Caroline Schmitt, et al.
Nature Genetics|January 17, 2012
Null alleles of ABCG2 encoding the breast cancer resistance protein define the new blood group system JuniorCarole Saison, Virginie Helias, Bryan A Ballif, et al.
Blood|July 18, 2020
Iron chelation rescues hemolytic anemia and skin photosensitivity in congenital erythropoietic porphyriaJean-Marc Blouin, Cécile Ged, Magalie Lalanne, et al.
Human Molecular Genetics|September 15, 2005
Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyriaCaroline Schmitt, Laurent Gouya, Eva Malonova, et al.
Biochemical and Biophysical Research Communications|October 12, 2019
Genetic background influences hepcidin response to iron imbalance in a mouse model of hemolytic anemia (Congenital erythropoietic porphyria)Thibaud Lefebvre, Sarah Millot, Emmanuel Richard, et al.
Molecular Genetics and Metabolism Reports|December 6, 2023
Management of erythropoietic protoporphyria with cholestatic liver disease: A case reportAntoine Poli, Camilla Frieri, Thibaud Lefebvre, et al.
Molecular Genetics and Metabolism|September 7, 2020
Kidney transplantation improves the clinical outcomes of Acute Intermittent PorphyriaHelene Lazareth, Neila Talbi, Nassim Kamar, 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.
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