Neerman-Arbez M - Search Results

1

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.

2

Composition of thrombi in zebrafish: similarities and distinctions with mammals.

Griffin MS, Dahlgren AR, Nagaswami C, Litvinov RI, Keeler K, Madenjian C, Fuentes R, Fish RJ, Neerman-Arbez M, Holinstat M, Adili R, Weisel JW, Shavit JA. Griffin MS, et al. Among authors: neerman arbez m. J Thromb Haemost. 2024 Apr;22(4):1056-1068. doi: 10.1016/j.jtha.2023.12.025. Epub 2023 Dec 30. J Thromb Haemost. 2024. PMID: 38160724

3

Deletion of the fibrinogen [correction of fibrogen] alpha-chain gene (FGA) causes congenital afibrogenemia.

Neerman-Arbez M, Honsberger A, Antonarakis SE, Morris MA. Neerman-Arbez M, et al. J Clin Invest. 1999 Jan;103(2):215-8. doi: 10.1172/JCI5471. J Clin Invest. 1999. PMID: 9916133 Free PMC article.

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. 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. 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. Hum Genet. 2001 Mar;108(3):237-40. doi: 10.1007/s004390100469. Hum Genet. 2001. PMID: 11354637

7

Fibrinogen gene mutations accounting for congenital afibrinogenemia.

Neerman-Arbez M. Neerman-Arbez M. Ann N Y Acad Sci. 2001;936:496-508. doi: 10.1111/j.1749-6632.2001.tb03536.x. Ann N Y Acad Sci. 2001. PMID: 11460507 Review.

8

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. 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.

9

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

10

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. 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.

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