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Journal of Analytical Toxicology|April 8, 2004
A rapid and sensitive high-performance liquid chromatography method for determination of embutramide (a Tanax or T61 component) in human blood with photodiode-array UV detectionEmuri Abe, Magali Delamoye, Bertille Mathieu, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|October 15, 2009
Characterization and expression of netrin-1 and its receptors UNC5B and DCC in human placentaMbarka Dakouane-Giudicelli, Christophe Duboucher, Joanne Fortemps, et al.
Forensic Science International|June 14, 2006
Allele frequencies and haplotypes of eight Y-short tandem repeats in Bantu population living in Central AfricaMaxime Lecerf, Mounir Filali, Gérard Grésenguet, et al.
Fertility and Sterility|January 24, 2012
Adiponectin and leptin systems in human endometrium during window of implantationEsther Dos Santos, Valérie Serazin, Corinne Morvan, et al.
Molecular Human Reproduction|November 8, 2014
Trophoblast syncytialisation necessitates mitochondrial function through estrogen-related receptor-γ activationDorothée Poidatz, Esther Dos Santos, Héloïse Gronier, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 5, 2008
Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodesIsmail Simsek, Philippe de Mazancourt, Marie-Hèléne Horellou, et al.
Forensic Science International|November 11, 2005
Study of the diagnostic value of iron in fresh water drowningGeoffroy Lorin de la Grandmaison, Michel Leterreux, Karine Lasseuguette, et al.
The International Journal of Developmental Biology|January 19, 2012
Hypoxia-inducible factor 1 controls the expression of the uncoordinated-5-B receptor, but not of netrin-1, in first trimester human placentaMbarka Dakouane-Giudicelli, Nadia Alfaidy, Perrine Bayle, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 5, 2008
An unusual clinical presentation of factor XIII deficiency and issues relating to the monitoring of factor XIII replacement therapyYesim Dargaud, Philippe de Mazancourt, Lucia Rugeri, et al.
Clinical Case Reports|November 30, 2022
Classical Ehlers-Danlos syndrome with severe kyphoscoliosis due to a novel pathogenic variant of <i>COL5A2</i>Malika Foy, Philippe de Mazancourt, Dominique Bremond Gignac, et al.
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