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Philippe de Moerloose Selected Research
Afibrinogenemia (Fibrinogen Deficiency)
06/2007
Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
11/2005
Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia.
12/2004
Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
12/2003
Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
Articles by Research Topic
Disease
4
Afibrinogenemia (Fibrinogen Deficiency)
06/2007 - 12/2003
3
Venous Thromboembolism
09/2008 - 03/2002
3
Antiphospholipid Syndrome (Antiphospholipid Antibody Syndrome)
04/2008 - 01/2004
2
Hemophilia A (Haemophilia)
02/2008 - 05/2006
1
Thrombosis (Thrombus)
10/2008
1
Thrombocytopenic Purpura (Thrombopenic Purpura)
04/2008
1
Thrombocytopenia (Thrombopenia)
12/2007
1
Tissue Adhesions
02/2005
1
Pulmonary Embolism
12/2004
1
Cardiovascular Diseases (Cardiovascular Disease)
12/2004
1
Acute Coronary Syndrome
12/2004
1
Thrombophlebitis
01/2004
Drug/Important Bio-Agent (IBA)
4
Fibrinogen (Factor I)
IBA
10/2008 - 12/2003
3
fibrin fragment D (D-dimer)
IBA
09/2008 - 09/2002
2
Factor V (Coagulation Factor V)
IBA
02/2008 - 05/2006
1
fibrinopeptides gamma
IBA
10/2008
1
Immunoglobulins (Immunoglobulin)
IBA
04/2008
1
Heparin (Liquaemin)
FDA Link
Generic
12/2007
1
Immunoglobulin G (IgG)
IBA
02/2005
1
Thromboplastin (Tissue Factor)
IBA
02/2005
1
Chemokine CCL2 (Monocyte Chemoattractant Protein 1)
IBA
02/2005
1
fluvastatin
FDA Link
02/2005
1
Antiphospholipid Antibodies
IBA
02/2005
1
Nonsense Codon (Nonsense Mutation)
IBA
12/2004
1
Apolipoprotein A-I (Apolipoprotein A1)
IBA
12/2004
1
Autoantibodies
IBA
12/2004
1
RNA (Ribonucleic Acid)
IBA
12/2004
1
Anticardiolipin Antibodies
IBA
01/2004
1
Homocysteine
IBA
03/2002