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The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A-like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor.
Ribba AN, Hilbert L, Lavergne JM, Fressinaud E, Boyer-Neumann C, Ternisien C, Juhan-Vague I, Goudemand J, Girma J, Mazurier C, Meyer D. Ribba AN, et al. Among authors: ternisien c. Blood. 2001 Feb 15;97(4):952-9. doi: 10.1182/blood.v97.4.952. Blood. 2001. PMID: 11159522 Free article.
Prothrombin index is an indirect marker of severe liver fibrosis.
Croquet V, Vuillemin E, Ternisien C, Pilette C, Oberti F, Gallois Y, Trossaert M, Rousselet MC, Chappard D, Calès P. Croquet V, et al. Among authors: ternisien c. Eur J Gastroenterol Hepatol. 2002 Oct;14(10):1133-41. doi: 10.1097/00042737-200210000-00015. Eur J Gastroenterol Hepatol. 2002. PMID: 12362105
Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one-stage and chromogenic factor VIII activity.
Trossaërt M, Boisseau P, Quemener A, Sigaud M, Fouassier M, Ternisien C, Lefrançois-Bettembourg A, Tesson C, Thomas C, Bezieau S. Trossaërt M, et al. Among authors: ternisien c. J Thromb Haemost. 2011 Mar;9(3):524-30. doi: 10.1111/j.1538-7836.2010.04174.x. J Thromb Haemost. 2011. PMID: 21166991 Free article.
[Acquired hemophilia A. A monocentric retrospective study of 39 patients].
Graveleau J, Trossaërt M, Leux C, Masseau A, Ternisien C, Néel A, Fouassier M, Agard C, Sigaud M, Hamidou M. Graveleau J, et al. Among authors: ternisien c. Rev Med Interne. 2013 Jan;34(1):4-11. doi: 10.1016/j.revmed.2012.10.367. Epub 2012 Dec 14. Rev Med Interne. 2013. PMID: 23246283 French.
97 results