de Moerloose P - Search Results

1

Identification and functional characterization of a novel nonsense mutation in FGA accounting for congenital afibrinogenemia in six Egyptian patients.

Abdel Wahab M, de Moerloose P, Fish RJ, Neerman-Arbez M. Abdel Wahab M, et al. Among authors: de moerloose p. Blood Coagul Fibrinolysis. 2010 Mar;21(2):164-7. doi: 10.1097/MBC.0b013e32833678d5. Blood Coagul Fibrinolysis. 2010. PMID: 20051841

2

Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.

Neerman-Arbez M, de Moerloose P, Bridel C, Honsberger A, Schönbörner A, Rossier C, Peerlinck K, Claeyssens S, Di Michele D, d'Oiron R, Dreyfus M, Laubriat-Bianchin M, Dieval J, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. Among authors: de moerloose p. Blood. 2000 Jul 1;96(1):149-52. Blood. 2000. PMID: 10891444 Free article.

3

Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G-->T.

Attanasio C, de Moerloose P, Antonarakis SE, Morris MA, Neerman-Arbez M. Attanasio C, et al. Among authors: de moerloose p. Blood. 2001 Mar 15;97(6):1879-81. doi: 10.1182/blood.v97.6.1879. Blood. 2001. PMID: 11238133 Free article.

4

Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.

Neerman-Arbez M, de Moerloose P, Honsberger A, Parlier G, Arnuti B, Biron C, Borg JY, Eber S, Meili E, Peter-Salonen K, Ripoll L, Vervel C, d'Oiron R, Staeger P, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. Among authors: de moerloose p. Hum Genet. 2001 Mar;108(3):237-40. doi: 10.1007/s004390100469. Hum Genet. 2001. PMID: 11354637

5

Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.

Vu D, Bolton-Maggs PH, Parr JR, Morris MA, de Moerloose P, Neerman-Arbez M. Vu D, et al. Among authors: de moerloose p. Blood. 2003 Dec 15;102(13):4413-5. doi: 10.1182/blood-2003-06-2141. Epub 2003 Jul 31. Blood. 2003. PMID: 12893758 Free article.

6

Severe factor XI deficiency in a Lebanese family: identification of a novel missense mutation (Trp501Cys) in the catalytic domain.

de Moerloose P, Germanos-Haddad M, Boehlen F, Neerman-Arbez M. de Moerloose P, et al. Blood Coagul Fibrinolysis. 2004 Apr;15(3):269-72. doi: 10.1097/00001721-200404000-00013. Blood Coagul Fibrinolysis. 2004. PMID: 15060426

7

Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.

Neerman-Arbez M, Germanos-Haddad M, Tzanidakis K, Vu D, Deutsch S, David A, Morris MA, de Moerloose P. Neerman-Arbez M, et al. Among authors: de moerloose p. Blood. 2004 Dec 1;104(12):3618-23. doi: 10.1182/blood-2004-06-2312. Epub 2004 Jul 29. Blood. 2004. PMID: 15284111 Free article.

8

Fluvastatin increases the expression of adhesion molecules, monocyte chemoattractant protein-1 and tissue factor in HUVEC stimulated by patient IgG fractions containing antiphospholipid antibodies.

Dunoyer-Geindre S, Dimitrova Y, Fish RJ, Satta N, Reber G, Kruithof EK, de Moerloose P. Dunoyer-Geindre S, et al. Among authors: de moerloose p. Thromb Haemost. 2005 Feb;93(2):339-45. doi: 10.1160/TH04-05-0297. Thromb Haemost. 2005. PMID: 15711752

9

Homozygosity for a Thr575Met missense mutation in the catalytic domain associated with factor XI deficiency.

Germanos-Haddad M, de Moerloose P, Boehlen F, Peyvandi F, Neerman-Arbez M. Germanos-Haddad M, et al. Among authors: de moerloose p. Haematologica. 2005 Mar;90(3):418-9. Haematologica. 2005. PMID: 15749683

10

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.

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