Netrins and Their Roles in Placental Angiogenesis

por Dakouane-Giudicelli, Mbarka, Alfaidy, Nadia, de Mazancourt, Philippe
Publicado 2014

A Simple RFLP-Based Method for HFE Gene Multiplex Amplification and Determination of Hereditary Hemochromatosis-Causing Mutation C282Y and H63D Variant with Highly Sensitive Determ...

por OGOUMA-AWORET, Ludmilla, RABES, Jean-Pierre, de MAZANCOURT, Philippe
Publicado 2020

Adiponectin promotes syncytialisation of BeWo cell line and primary trophoblast cells

por Benaitreau, Delphine, Santos, Esther Dos, Leneveu, Marie-Christine, De Mazancourt, Philippe, Pecquery, René, Dieudonné, Marie-Noëlle
Publicado 2010

Classical Ehlers–Danlos syndrome with severe kyphoscoliosis due to a novel pathogenic variant of COL5A2

por Foy, Malika, de Mazancourt, Philippe, Bremond Gignac, Dominique, Gillas, Fabrice, Trigui, Nawel, Mekki, Ahmed, Carlier, Robert, Benistan, Karelle
Publicado 2022

Mild forms of hypophosphatasia mostly result from dominant negative effect of severe alleles or from compound heterozygosity for severe and moderate alleles

por Fauvert, Delphine, Brun-Heath, Isabelle, Lia-Baldini, Anne-Sophie, Bellazi, Linda, Taillandier, Agnès, Serre, Jean-Louis, de Mazancourt, Philippe, Mornet, Etienne
Publicado 2009

Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria

por Hadjali‐Saichi, Soraya, de Mazancourt, Philippe, Tapon‐Bretaudière, Jacqueline, Mirault, Tristan, Guenounou, Kahina, Frigaa, Issam, Fischer, Anne‐Marie, Chafa, Ouerdia, Helley, Dominique
Publicado 2022

Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) Programs

por Boudjenah, Radia, Molina-Gomes, Denise, Torre, Antoine, Boitrelle, Florence, Taieb, Stéphane, Dos Santos, Esther, Wainer, Robert, de Mazancourt, Philippe, Selva, Jacqueline, Vialard, François
Publicado 2014

TWEAK Appears as a Modulator of Endometrial IL-18 Related Cytotoxic Activity of Uterine Natural Killers

por Petitbarat, Marie, Rahmati, Mona, Sérazin, Valérie, Dubanchet, Sylvie, Morvan, Corinne, Wainer, Robert, de Mazancourt, Philippe, Chaouat, Gérard, Foidart, Jean-Michel, Munaut, Carine, Lédée, Nathalie
Publicado 2011

Genetic Polymorphisms Influence the Ovarian Response to rFSH Stimulation in Patients Undergoing In Vitro Fertilization Programs with ICSI

por Boudjenah, Radia, Molina-Gomes, Denise, Torre, Antoine, Bergere, Marianne, Bailly, Marc, Boitrelle, Florence, Taieb, Stéphane, Wainer, Robert, Benahmed, Mohamed, de Mazancourt, Philippe, Selva, Jacqueline, Vialard, François
Publicado 2012

A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder

por Foy, Malika, De Mazancourt, Philippe, Métay, Corinne, Carlier, Robert, Allamand, Valérie, Gartioux, Corine, Gillas, Fabrice, Miri, Nawel, Jobic, Valérie, Mekki, Ahmed, Richard, Pascale, Michot, Caroline, Benistan, Karelle
Publicado 2021

A severe case of PLOD1 ‐related kyphoscoliotic Ehlers–Danlos syndrome associated with several arterial and venous complications: A case report

por Foy, Malika, Métay, Corinne, Frank, Michael, Denarié, Nicolas, Adham, Salma, Billon, Clarisse, Legrand, Anne, Jeunemaitre, Xavier, Gillas, Fabrice, Gaudon, Karen, De Mazancourt, Philippe, Mekki, Ahmed, Carlier, Robert, Benistan, Karelle
Publicado 2023