Neerman-Arbez M - Search Results

1

Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A.

Vilar R, Casini A, Fournel A, Mourey G, Neerman-Arbez M. Vilar R, et al. Thromb Res. 2020 Sep;193:5-8. doi: 10.1016/j.thromres.2020.05.040. Epub 2020 May 28. Thromb Res. 2020. PMID: 32497950 No abstract available.

2

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.

3

The molecular basis of inherited afibrinogenaemia.

Neerman-Arbez M. Neerman-Arbez M. Thromb Haemost. 2001 Jul;86(1):154-63. Thromb Haemost. 2001. PMID: 11487003 Review.

4

Molecular basis of fibrinogen deficiency.

Neerman-Arbez M. Neerman-Arbez M. Pathophysiol Haemost Thromb. 2006;35(1-2):187-98. doi: 10.1159/000093566. Pathophysiol Haemost Thromb. 2006. PMID: 16855369 Review.

5

Molecular mechanisms accounting for fibrinogen deficiency: from large deletions to intracellular retention of misfolded proteins.

Vu D, Neerman-Arbez M. Vu D, et al. J Thromb Haemost. 2007 Jul;5 Suppl 1:125-31. doi: 10.1111/j.1538-7836.2007.02465.x. J Thromb Haemost. 2007. PMID: 17635718 Free article. Review.

6

To aggregate or not to aggregate..

Neerman-Arbez M. Neerman-Arbez M. J Thromb Haemost. 2007 Oct;5(10):1997-8. doi: 10.1111/j.1538-7836.2007.02608.x. J Thromb Haemost. 2007. PMID: 17883695 Free article. No abstract available.

7

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. Blood Coagul Fibrinolysis. 2008 Oct;19(7):697-9. doi: 10.1097/MBC.0b013e3282f544ee. Blood Coagul Fibrinolysis. 2008. PMID: 18832913

8

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. Blood Coagul Fibrinolysis. 2009 Jul;20(5):385-7. doi: 10.1097/MBC.0b013e328329f2a0. Blood Coagul Fibrinolysis. 2009. PMID: 19417632 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

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. 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.

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