de Moerloose P - Search Results

1

Pharmacology, Efficacy and Safety of a Triple-Secured Fibrinogen Concentrate in Children Less than or Equal to 12 Years with Afibrinogenaemia.

Djambas Khayat C, El Khorassani M, Aytaç S, Harroche A, Dahmane A, Pujol S, Henriet C, de Moerloose P, Bridey F. Djambas Khayat C, et al. Among authors: de moerloose p. Thromb Haemost. 2020 Jun;120(6):957-967. doi: 10.1055/s-0040-1710015. Epub 2020 May 11. Thromb Haemost. 2020. PMID: 32392604 Clinical Trial.

2

Value of liquid crystal contact thermography and plasma level of D-dimer for screening of deep venous thrombosis following general abdominal surgery.

Bounameaux H, Khabiri E, Huber O, Schneider PA, Didier D, de Moerloose P, Reber G. Bounameaux H, et al. Among authors: de moerloose p. Thromb Haemost. 1992 Jun 1;67(6):603-6. Thromb Haemost. 1992. PMID: 1509399 Clinical Trial.

3

D-Dimer for venous thromboembolism diagnosis: 20 years later.

Righini M, Perrier A, De Moerloose P, Bounameaux H. Righini M, et al. Among authors: de moerloose p. J Thromb Haemost. 2008 Jul;6(7):1059-71. doi: 10.1111/j.1538-7836.2008.02981.x. Epub 2008 Jul 1. J Thromb Haemost. 2008. PMID: 18419743 Free article. Review.

4

Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation.

Djambas Khayat C, Salem N, Chouery E, Corbani S, Moix I, Nicolas E, Morris MA, de Moerloose P, Mégarbané A. Djambas Khayat C, et al. Among authors: de moerloose p. Haemophilia. 2008 Jul;14(4):709-16. doi: 10.1111/j.1365-2516.2008.01760.x. Epub 2008 May 7. Haemophilia. 2008. PMID: 18479430

5

A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis.

Robert-Ebadi H, Le Querrec A, de Moerloose P, Gandon-Laloum S, Borel Derlon A, Neerman-Arbez M. Robert-Ebadi H, et al. Among authors: de moerloose p. Blood Coagul Fibrinolysis. 2008 Oct;19(7):697-9. doi: 10.1097/MBC.0b013e3282f544ee. Blood Coagul Fibrinolysis. 2008. PMID: 18832913

6

A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.

Robert-Ebadi H, de Moerloose P, El Khorassani M, El Khattab M, Neerman-Arbez M. Robert-Ebadi H, et al. Among authors: de moerloose p. Blood Coagul Fibrinolysis. 2009 Jul;20(5):385-7. doi: 10.1097/MBC.0b013e328329f2a0. Blood Coagul Fibrinolysis. 2009. PMID: 19417632 Review.

7

Congenital fibrinogen disorders.

de Moerloose P, Neerman-Arbez M. de Moerloose P, et al. Semin Thromb Hemost. 2009 Jun;35(4):356-66. doi: 10.1055/s-0029-1225758. Epub 2009 Jul 13. Semin Thromb Hemost. 2009. PMID: 19598064 Review.

8

A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family.

Levrat E, Aboukhamis I, de Moerloose P, Farho J, Chamaa S, Reber G, Fort A, Neerman-Arbez M. Levrat E, et al. Among authors: de moerloose p. Blood Coagul Fibrinolysis. 2011 Mar;22(2):148-50. doi: 10.1097/MBC.0b013e32834330d9. Blood Coagul Fibrinolysis. 2011. PMID: 21245743

9

Platelet reactivity is a stable and global phenomenon in aspirin-treated cardiovascular patients.

Zufferey A, Reny JL, Combescure C, de Moerloose P, Sanchez JC, Fontana P. Zufferey A, et al. Among authors: de moerloose p. Thromb Haemost. 2011 Sep;106(3):466-74. doi: 10.1160/TH11-04-0226. Epub 2011 Jul 4. Thromb Haemost. 2011. PMID: 21725581

10

Acquired factor XIII deficiency: a therapeutic challenge.

Boehlen F, Casini A, Chizzolini C, Mansouri B, Kohler HP, Schroeder V, Reber G, de Moerloose P. Boehlen F, et al. Among authors: de moerloose p. Thromb Haemost. 2013 Mar;109(3):479-87. doi: 10.1160/TH12-08-0604. Epub 2013 Jan 10. Thromb Haemost. 2013. PMID: 23306660 Review.

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