Emmerich J - Search Results

1

[Protein C deficiency: cause or coincidence in arterial vascular accidents].

Emmerich J, Alhenc-Gelas M, Gandrille S, Laurian C, Capron L, Aiach M, Fiessinger JN. Emmerich J, et al. Presse Med. 1993 May 15;22(17):830. Presse Med. 1993. PMID: 8316554 French. No abstract available.

2

[A new cause of familial thrombophilia: resistance to the effect of activated protein C].

Emmerich J, Alhenc-Gelas M, Gandrille S, Fiessinger JN, Aiach M. Emmerich J, et al. Presse Med. 1994 Sep 24;23(28):1285-7. Presse Med. 1994. PMID: 7984524 French.

3

[Treatment with octreotide for functional obstructions in scleroderma].

Emmerich J, Roux ME, Capron L, Fiessinger JN. Emmerich J, et al. Presse Med. 1992 Feb 22;21(7):316-7. Presse Med. 1992. PMID: 1532651 French. No abstract available.

4

[Heparin-fluindione relay. Comparison of 2 prescription models].

Le Floch E, Alhenc-Gelas M, Paul JF, Emmerich J, Aiach M, Fiessinger JN. Le Floch E, et al. Among authors: emmerich j. Presse Med. 1995 May 6-13;24(17):828. Presse Med. 1995. PMID: 7630875 Clinical Trial. French. No abstract available.

5

[Apropos of the resistance to activated protein-C in venous thromboembolic accidents].

Alhenc-Gelas M, Emmerich J, Aiach M, Fiessinger JN. Alhenc-Gelas M, et al. Among authors: emmerich j. Presse Med. 1995 Apr 29;24(16):784. Presse Med. 1995. PMID: 7784421 French. No abstract available.

6

Met 358 to Arg mutation of alpha 1-antitrypsin associated with protein C deficiency in a patient with mild bleeding tendency.

Vidaud D, Emmerich J, Alhenc-Gelas M, Yvart J, Fiessinger JN, Aiach M. Vidaud D, et al. Among authors: emmerich j. J Clin Invest. 1992 May;89(5):1537-43. doi: 10.1172/JCI115746. J Clin Invest. 1992. PMID: 1569192 Free PMC article.

7

Mechanism of protein C deficiency in a patient with arginine 358 alpha 1-antitrypsin (Pittsburgh mutation): role in the maintenance of hemostatic balance.

Emmerich J, Alhenc-Gelas M, Gandrille S, Guichet C, Fiessinger JN, Aiach M. Emmerich J, et al. J Lab Clin Med. 1995 Apr;125(4):531-9. J Lab Clin Med. 1995. PMID: 7706910

8

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. Among authors: emmerich j. Blood Coagul Fibrinolysis. 1995 Feb;6(1):35-41. doi: 10.1097/00001721-199502000-00006. Blood Coagul Fibrinolysis. 1995. PMID: 7795152 Review.

9

First de novo mutations in the protein C gene of two patients with type I deficiency: a missense mutation and a splice site deletion.

Gandrille S, Jude B, Alhenc-Gelas M, Emmerich J, Aiach M. Gandrille S, et al. Among authors: emmerich j. Blood. 1994 Oct 15;84(8):2566-70. Blood. 1994. PMID: 7919373 Free article.

10

[Percutaneous thrombo-aspiration as a substitute for surgical embolectomy using Fogarty's catheter].

Emmerich J, Beyssen B, Fiessinger JN, Gaux JC. Emmerich J, et al. Presse Med. 1993 Nov 13;22(35):1765-6. Presse Med. 1993. PMID: 8115314 Review. French. No abstract available.

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