de Moerloose P - Search Results

1

Can the phenotype of inherited fibrinogen disorders be predicted?

Casini A, de Moerloose P. Casini A, et al. Among authors: de moerloose p. Haemophilia. 2016 Sep;22(5):667-75. doi: 10.1111/hae.12967. Epub 2016 Jun 13. Haemophilia. 2016. PMID: 27293018 Review.

2

Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion.

Vu D, de Moerloose P, Batorova A, Lazur J, Palumbo L, Neerman-Arbez M. Vu D, et al. Among authors: de moerloose p. J Med Genet. 2005 Sep;42(9):e57. doi: 10.1136/jmg.2005.033530. J Med Genet. 2005. PMID: 16141000 Free PMC article.

3

Rare bleeding disorders.

Peyvandi F, Cattaneo M, Inbal A, De Moerloose P, Spreafico M. Peyvandi F, et al. Among authors: de moerloose p. Haemophilia. 2008 Jul;14 Suppl 3:202-10. doi: 10.1111/j.1365-2516.2008.01751.x. Haemophilia. 2008. PMID: 18510543 Review.

4

Treatment of congenital fibrinogen disorders.

de Moerloose P, Neerman-Arbez M. de Moerloose P, et al. Expert Opin Biol Ther. 2008 Jul;8(7):979-92. doi: 10.1517/14712598.8.7.979. Expert Opin Biol Ther. 2008. PMID: 18549327 Review.

5

A survey of adherence to haemophilia therapy in six European countries: results and recommendations.

De Moerloose P, Urbancik W, Van Den Berg HM, Richards M. De Moerloose P, et al. Haemophilia. 2008 Sep;14(5):931-8. doi: 10.1111/j.1365-2516.2008.01843.x. Epub 2008 Aug 4. Haemophilia. 2008. PMID: 18684125

6

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

7

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.

8

Diagnosis of mild bleeding disorders.

de Moerloose P, Levrat E, Fontana P, Boehlen F. de Moerloose P, et al. Swiss Med Wkly. 2009 Jun 13;139(23-24):327-32. doi: 10.4414/smw.2009.12476. Swiss Med Wkly. 2009. PMID: 19529990 Free article. Review.

9

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.

10

Fibrinogen and the risk of thrombosis.

de Moerloose P, Boehlen F, Neerman-Arbez M. de Moerloose P, et al. Semin Thromb Hemost. 2010 Feb;36(1):7-17. doi: 10.1055/s-0030-1248720. Epub 2010 Apr 13. Semin Thromb Hemost. 2010. PMID: 20391292 Review.

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