Alhenc-Gelas M - Search Results

1

Fetal intracerebral hemorrhage in familial thrombophilia.

Crespin M, Alhenc-Gelas M, Grangé G, Fallet-Bianco C, Fontenay M. Crespin M, et al. Pediatr Neurol. 2009 Oct;41(4):291-3. doi: 10.1016/j.pediatrneurol.2009.04.027. Pediatr Neurol. 2009. PMID: 19748050

2

Intracerebral hemorrhage associated with a novel antithrombin gene mutation in a neonate.

Baud O, Picard V, Durand P, Duchemin J, Proulle V, Alhenc-Gelas M, Devictor D, Dreyfus M. Baud O, et al. J Pediatr. 2001 Nov;139(5):741-3. doi: 10.1067/mpd.2001.118191. J Pediatr. 2001. PMID: 11713457

3

Heerlen polymorphism associated with type III protein S deficiency and factor V Leiden mutation in a Polish patient with deep vein thrombosis.

Wypasek E, Potaczek DP, Alhenc-Gelas M, Undas A. Wypasek E, et al. Blood Coagul Fibrinolysis. 2014 Jan;25(1):84-5. doi: 10.1097/MBC.0b013e328365032c. Blood Coagul Fibrinolysis. 2014. PMID: 24365770

4

Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.

Boinot C, Borgel D, Kitzis A, Guicheteau M, Aiach M, Alhenc-Gelas M. Boinot C, et al. Blood Coagul Fibrinolysis. 2003 Feb;14(2):191-6. doi: 10.1097/01.mbc.0000046180.72384.39. Blood Coagul Fibrinolysis. 2003. PMID: 12632031

5

[Coagulation factor mutations and thrombosis].

Aiach M, Alhenc-Gelas M, Borgel D, Emmerich J, Gandrille S, Picard V. Aiach M, et al. Med Sci (Paris). 2006 Nov;22(11):985-9. doi: 10.1051/medsci/20062211985. Med Sci (Paris). 2006. PMID: 17101102 Free article. Review. French.

6

Influence of three potential genetic risk factors for thrombosis in 43 families carrying the factor V Arg 506 to Gln mutation.

Le Cam-Duchez V, Gandrille S, Trégouët D, Alhenc-Gelas M, Emmerich J, Fiessinger JN, Borg JY, Aiach M. Le Cam-Duchez V, et al. Br J Haematol. 1999 Sep;106(4):889-97. doi: 10.1046/j.1365-2141.1999.01661.x. Br J Haematol. 1999. PMID: 10519989 Free article.

7

Venous thromboembolic disease: risk factors and laboratory investigation.

Alhenc-Gelas M, Aiach M, de Moerloose P. Alhenc-Gelas M, et al. Semin Vasc Med. 2001;1(1):81-8. doi: 10.1055/s-2001-14544. Semin Vasc Med. 2001. PMID: 15199517 Review.

8

Incidence of activated protein C resistance caused by the ARG 506 GLN mutation in factor V in 113 unrelated symptomatic protein C-deficient patients. The French Network on the behalf of INSERM.

Gandrille S, Greengard JS, Alhenc-Gelas M, Juhan-Vague I, Abgrall JF, Jude B, Griffin JH, Aiach M. Gandrille S, et al. Blood. 1995 Jul 1;86(1):219-24. Blood. 1995. PMID: 7795227 Free article.

9

Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes.

Picard V, Bauters A, Khairy M, Ochat N, Jude B, Aiach M, Alhenc-Gelas M. Picard V, et al. Thromb Haemost. 2005 Jan;93(1):57-62. doi: 10.1160/TH04-08-0477. Thromb Haemost. 2005. PMID: 15630491

10

Protein C and protein S deficiencies.

Aiach M, Borgel D, Gaussem P, Emmerich J, Alhenc-Gelas M, Gandrille S. Aiach M, et al. Semin Hematol. 1997 Jul;34(3):205-16. Semin Hematol. 1997. PMID: 9241706 Review.

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