Recombinant human factor VIIa (rFVIIa) in hemophilia: mode of action and evidence to date

por Giansily-Blaizot, Muriel, Schved, Jean-François
Publicado en Ther Adv Hematol (2017)

SULFs in human neoplasia: implication as progression and prognosis factors

por Bret, Caroline, Moreaux, Jérôme, Schved, Jean-François, Hose, Dirk, Klein, Bernard
Publicado 2011

Homozygous mutation of the 5'UTR region of the L-Ferritin gene in the hereditary hyperferritinemia cataract syndrome and its impact on the phenotype

por Giansily-Blaizot, Muriel, Cunat, Séverine, Moulis, Grégory, Schved, Jean-François, Aguilar-Martinez, Patricia
Publicado 2013

HAMP promoter mutation nc.-153C>T in non p.C282Y homozygous patients with iron overload

por Aguilar-Martinez, Patricia, Giansily-Blaizot, Muriel, Bismuth, Michael, Cunat, Séverine, Igual, Hélène, Schved, Jean François
Publicado 2010

Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants

por Aguilar-Martinez, Patricia, Grandchamp, Bernard, Cunat, Séverine, Cadet, Estelle, Blanc, François, Nourrit, Marlène, Lassoued, Kaiss, Schved, Jean-François, Rochette, Jacques
Publicado 2011

Design of a prospective observational study on the effectiveness and real-world usage of recombinant factor VIII Fc (rFVIIIFc) compared with conventional products in haemophilia A:...

por Oldenburg, Johannes, Hay, Charles R M, Jiménez-Yuste, Víctor, Peyvandi, Flora, Schved, Jean-François, Szamosi, Johan, Winding, Bent, Lethagen, Stefan
Publicado en BMJ Open (2019)

Long-Term Antithrombotic Treatments Prescribed for Cardiovascular Diseases in Patients with Hemophilia: Results from the French Registry

por Guillet, Benoît, Cayla, Guillaume, Lebreton, Aurélien, Trillot, Nathalie, Wibaut, Bénédicte, Falaise, Céline, Castet, Sabine, Gautier, Philippe, Claeyssens, Ségolène, Schved, Jean-François
Publicado en Thromb Haemost (2021)

Expression of genes encoding for proteins involved in heparan sulphate and chondroitin sulphate chain synthesis and modification in normal and malignant plasma cells

por Bret, Caroline, Hose, Dirk, Reme, Thierry, Sprynski, Anne-Catherine, Mahtouk, Karène, Schved, Jean-François, Quittet, Philippe, Rossi, Jean-François, Goldschmidt, Hartmut, Klein, Bernard
Publicado 2009

Evaluation of hemostasis and endothelial function in patients with paroxysmal nocturnal hemoglobinuria receiving eculizumab

por Helley, Dominique, de Latour, Régis Peffault, Porcher, Raphaël, Rodrigues, Celso Arrais, Galy-Fauroux, Isabelle, Matheron, Jeanne, Duval, Arnaud, Schved, Jean-François, Fischer, Anne-Marie, Socié, Gérard
Publicado 2010

Expression Map of the Human Exome in CD34+ Cells and Blood Cells: Increased Alternative Splicing in Cell Motility and Immune Response Genes

por Tondeur, Sylvie, Pangault, Céline, Le Carrour, Tanguy, Lannay, Yoann, Benmahdi, Rima, Cubizolle, Aurélie, Assou, Said, Pantesco, Véronique, Klein, Bernard, Hamamah, Samir, Schved, Jean-François, Fest, Thierry, De Vos, John
Publicado 2010

The Southern French registry of genetic hemochromatosis: a tool for determining clinical prevalence of the disorder and genotype penetrance

por Aguilar-Martinez, Patricia, Bismuth, Michael, Blanc, François, Blanc, Pierre, Cunat, Severine, Dereure, Olivier, Dujols, Pierre, Giansily-Blaizot, Muriel, Jorgensen, Christian, Konate, Amadou, Larrey, Dominique, Le Quellec, Alain, Mura, Thibault, Raingeard, Isabelle, Ramos, Jeanne, Renard, Eric, Rousseau, Florence, Schved, Jean-François, Picot, Marie-Christine
Publicado 2010

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1

por Morange, Pierre-Emmanuel, Bezemer, Irene, Saut, Noémie, Bare, Lance, Burgos, Gwenaelle, Brocheton, Jessy, Durand, Hervé, Biron-Andreani, Christine, Schved, Jean-Francois, Pernod, Gilles, Galan, Pilar, Drouet, Ludovic, Zelenika, Diana, Germain, Marine, Nicaud, Viviane, Heath, Simon, Ninio, Ewa, Delluc, Aurélien, Münzel, Thomas, Zeller, Tanja, Brand-Herrmann, Stefan-Martin, Alessi, Marie-Christine, Tiret, Laurence, Lathrop, Mark, Cambien, François, Blankenberg, Stefan, Emmerich, Joseph, Trégouët, David-Alexandre, Rosendaal, Frits R.
Publicado 2010

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1

por Morange, Pierre-Emmanuel, Bezemer, Irene, Saut, Noémie, Bare, Lance, Burgos, Gwenaelle, Brocheton, Jessy, Durand, Hervé, Biron-Andreani, Christine, Schved, Jean-Francois, Pernod, Gilles, Galan, Pilar, Drouet, Ludovic, Zelenika, Diana, Germain, Marine, Nicaud, Viviane, Heath, Simon, Ninio, Ewa, Delluc, Aurélien, Münzel, Thomas, Zeller, Tanja, Brand-Herrmann, Stefan-Martin, Alessi, Marie-Christine, Tiret, Laurence, Lathrop, Mark, Cambien, François, Blankenberg, Stefan, Emmerich, Joseph, Trégouët, David-Alexandre, Rosendaal, Frits R.
Publicado 2010