Alhenc-Gelas M - Search Results

1

Late onset of clinical symptoms and recurrent ecchymotic skin lesions in a 12-year-old girl with a severe double heterozygous protein C deficiency.

Loop M, Ferster A, Corazza F, Alhenc-Gelas M, Demulder A. Loop M, et al. J Pediatr Hematol Oncol. 2004 Jan;26(1):2-4. doi: 10.1097/00043426-200401000-00002. J Pediatr Hematol Oncol. 2004. PMID: 14707701

2

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.

3

[Skin necrosis during long-term fluindione treatment revealing protein C deficiency].

Merklen-Djafri C, Mazurier I, Samama MM, Alhenc-Gelas M, Tortel MC, Cribier B, Roth B, Batard ML. Merklen-Djafri C, et al. Ann Dermatol Venereol. 2012 Mar;139(3):199-203. doi: 10.1016/j.annder.2011.12.018. Epub 2012 Jan 30. Ann Dermatol Venereol. 2012. PMID: 22401685 French.

4

Protein C infusion in a patient with inherited protein C deficiency caused by two missense mutations: Arg 178 to Gln and Arg-1 to His.

Alhenc-Gelas M, Emmerich J, Gandrille S, Aubry ML, Benaily N, Fiessinger JN, Aiach M. Alhenc-Gelas M, et al. Blood Coagul Fibrinolysis. 1995 Feb;6(1):35-41. doi: 10.1097/00001721-199502000-00006. Blood Coagul Fibrinolysis. 1995. PMID: 7795152 Review.

5

Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.

Borgel D, Duchemin J, Alhenc-Gelas M, Matheron C, Aiach M, Gandrille S. Borgel D, et al. J Lab Clin Med. 1996 Aug;128(2):218-27. doi: 10.1016/s0022-2143(96)90015-3. J Lab Clin Med. 1996. PMID: 8765219 Clinical Trial.

6

Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis.

Borensztajn K, Chafa O, Alhenc-Gelas M, Salha S, Reghis A, Fischer AM, Tapon-Bretaudière J. Borensztajn K, et al. Br J Haematol. 2002 Apr;117(1):168-71. doi: 10.1046/j.1365-2141.2002.03397.x. Br J Haematol. 2002. PMID: 11918550 Free article.

7

Two novel mutations responsible for hereditary type I protein C deficiency: characterization by denaturing gradient gel electrophoresis.

Gandrille S, Vidaud M, Aiach M, Alhenc-Gelas M, Fischer AM, Gouault-Heilman M, Toulon P, Fiessinger JN, Goossens M. Gandrille S, et al. Hum Mutat. 1992;1(6):491-500. doi: 10.1002/humu.1380010607. Hum Mutat. 1992. PMID: 1301959

8

Protein C concentrates in a neonate with a cerebral venous thrombosis due to heterozygous type 1 protein C deficiency.

Tardy-Poncet B, Rayet I, Damon G, Alhenc-Gelas M, Dutour N, Lavocat MP. Tardy-Poncet B, et al. Thromb Haemost. 2001 Jun;85(6):1118-9. Thromb Haemost. 2001. PMID: 11434695 No abstract available.

9

Venous thrombosis in older people: prevalence of the factor V gene mutation Q506.

André E, Siguret V, Alhenc-Gelas M, Saint-Jean O, Gaussem P. André E, et al. J Am Geriatr Soc. 1998 Dec;46(12):1545-9. doi: 10.1111/j.1532-5415.1998.tb01540.x. J Am Geriatr Soc. 1998. PMID: 9848816

10

[Venous thrombosis in a pregnant woman heterozygous for factor V Q506 mutation].

Chabane MH, Alhenc-Gelas M, Pathier D, Siguret V, Andreux JP, Gaussem P. Chabane MH, et al. Ann Biol Clin (Paris). 1998 Jan-Feb;56(1):112-3. Ann Biol Clin (Paris). 1998. PMID: 9754234 Free article. French. No abstract available.

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