de Moerloose P - Search Results

1

Hypodysfibrinogenaemia due to production of mutant fibrinogen alpha-chains lacking fibrinopeptide A and polymerisation knob 'A'.

Vorjohann S, Fish RJ, Biron-Andréani C, Nagaswami C, Weisel JW, Boulot P, Reyftmann L, de Moerloose P, Neerman-Arbez M. Vorjohann S, et al. Among authors: de moerloose p. Thromb Haemost. 2010 Nov;104(5):990-7. doi: 10.1160/TH10-03-0161. Epub 2010 Aug 30. Thromb Haemost. 2010. PMID: 20806111 Free PMC article.

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

Fibrinogen Geneva, a new case of A alpha 16 Arg----Cys dysfibrinogenaemia.

Furlan M, Bögli C, Hofer A, Bouvier CA, de Moerloose P. Furlan M, et al. Among authors: de moerloose p. Blood Coagul Fibrinolysis. 1990 Jun;1(2):139-43. Blood Coagul Fibrinolysis. 1990. PMID: 2130925

4

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.

5

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.

6

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

7

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.

8

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

9

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.

10

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

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