P. Mazancourt

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LETTERS TO THE EDITOR: Four cases of hypofibrinogenemia associated with four novel mutations

M. Bertrand, C. Vinciguerra, M. Hanss, 2005, Journal of thrombosis and haemostasis : JTH.

EG-VEGF controls placental growth and survival in normal and pathological pregnancies: case of fetal growth restriction (FGR)

S. Brouillet, P. de Mazancourt, M. Dieudonné, 2012, Cellular and Molecular Life Sciences.

Antiproliferative Effects of Adiponectin on Human Trophoblastic Cell Lines JEG-3 and BeWo1

M. Dieudonné, M. Leneveu, R. Pecquery, 2009, Biology of reproduction.

Mitogenic effects of pertussis toxin-sensitive G-protein α subunits: The mitogenic action of αi2 in NIH 3T3 cells is mimicked by αi1, but not αi3

S. Hermouet, A. Spiegel, P. Mazancourt, 1993 .

N6-phenylisopropyladenosine stimulates in normal and inhibits in adrenalectomized rats the low K M cyclic AMP phosphodiesterase in the brain

Y. Giudicelli, P. Mazancourt, 1984, Brain Research.

Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

M. Trossaërt, É. Fressinaud, M. Trossaert, 2004, Journal of thrombosis and haemostasis : JTH.

DNA genotyping of unbuffered formalin fixed paraffin embedded tissues.

M. Durigon, P. Mazancourt, K. Crainic, 2002, Forensic science international.

The vascular endothelial growth factor (VEGF) +405 G/C polymorphism and its relationship with recurrent implantation failure in women in an IVF programme with ICSI

F. Vialard, J. Selva, R. Wainer, 2012, Journal of Assisted Reproduction and Genetics.

Are the metabolic characteristics of congenital intraspinal lipoma cells identical to, or different from normal adipocytes?

J. Hirsch, Y. Giudicelli, D. Lacasa, 2004, Child's Nervous System.

Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency

J. Peynet, C. Mazurier, L. Guillon, 2006, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Y-STR AS PROOF OF RAPE WHEN SPERM CELLS CANNOT BE FOUND

M. Durigon, P. Mazancourt, C. Duverneuil, 2002 .

Direct control of a large conductance K+-selective channel by G-proteins in adrenal chromaffin granule membranes

E. Rojas, N. Arispe, P. Mazancourt, 1995, The Journal of Membrane Biology.

Gamete cytogenetic study in couples with implantation failure: aneuploidy rate is increased in both couple members

F. Vialard, J. Selva, R. Wainer, 2008, Journal of Assisted Reproduction and Genetics.

Prenatal diagnosis of a 45,X male with a SRY‐bearing chromosome 21

J. Roume, M. Senat, V. Nataf, 2002, Prenatal diagnosis.

A single session of anodal transcranial direct current stimulation applied over the affected primary motor cortex does not alter gait parameters in chronic stroke survivors

D. Pradon, R. Zory, N. Roche, 2019, Neurophysiologie Clinique.

EG-VEGF controls placental growth and survival in normal and pathological pregnancies: case of fetal growth restriction (FGR)

S. Brouillet, M. Dieudonné, N. Alfaidy, 2013, Cellular and Molecular Life Sciences.

PreImplantation factor (PIF) promotes human trophoblast invasion

M. Dieudonné, F. Vialard, L. Loeuillet, 2014 .

Activated protein C sensitivity ratio in pregnant women at delivery

Y. Giudicelli, J. Borg, P. Mazancourt, 1996, British journal of haematology.

X‐chromosome inactivation in female patients with Fabry disease

A. Hagège, P. de Mazancourt, O. Dubourg, 2016, Clinical genetics.

Array Comparative Genomic Hybridization in Prenatal Diagnosis: Another Experience

J. Roume, P. de Mazancourt, V. Sérazin, 2009, Fetal Diagnosis and Therapy.

Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

P. de Mazancourt, P. Calès, S. Michalak, 2007, Journal of thrombosis and haemostasis : JTH.

Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations(γAla341Thr, Bβ Tyr326Cys and Aα Asp496Asn)

C. Négrier, M. Hanss, P. French, 2007, Thrombosis and Haemostasis.

Y. Giudicelli, D. Lacasa, P. Goldsmith, 1996 .

Thrombin generation in patients with factor XI deficiency and clinical bleeding risk

P. de Mazancourt, C. Négrier, Y. Dargaud, 2010, Haemophilia : the official journal of the World Federation of Hemophilia.

A heterozygous 4-bp deletion mutation in the Gs alpha gene (GNAS1) in a patient with Albright hereditary osteodystrophy.

P. Gejman, P. de Mazancourt, L. Weinstein, 1992, Genomics.

A matrix factorization and its application to large-scale linear programming

P. F. De Mazancourt, P. Mazancourt, 1990 .

Use of Genotypic Identification by sodA Sequencing in a Prospective Study To Examine the Distribution of Coagulase-Negative Staphylococcus Species among Strains Recovered during Septic Orthopedic Surgery and Evaluate Their Significance

P. de Mazancourt, P. Trieu-Cuot, J. Gaillard, 2005, Journal of Clinical Microbiology.