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Acquired von Willebrand syndrome: from pathophysiology to management.
Veyradier A, Jenkins CS, Fressinaud E, Meyer D. Veyradier A, et al. Thromb Haemost. 2000 Aug;84(2):175-82. Thromb Haemost. 2000. PMID: 10959686 Review. No abstract available.
Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis.
Veyradier A, Caron C, Ternisien C, Wolf M, Trossaert M, Fressinaud E, Goudemand J. Veyradier A, et al. Haemophilia. 2011 Nov;17(6):944-51. doi: 10.1111/j.1365-2516.2011.02499.x. Epub 2011 Mar 3. Haemophilia. 2011. PMID: 21371195
[Von Willebrand disease: from diagnosis to treatment].
Fressinaud E, Meyer D. Fressinaud E, et al. Rev Prat. 2005 Dec 31;55(20):2209-18. Rev Prat. 2005. PMID: 16519045 Review. French.
A new mutation, S1285F, within the A1 loop of von Willebrand factor induces a conformational change in A1 loop with abnormal binding to platelet GPIb and botrocetin causing type 2M von Willebrand disease.
Stepanian A, Ribba AS, Lavergne JM, Fressinaud E, Juhan-Vague I, Mazurier C, Girma JP, Meyer D. Stepanian A, et al. Br J Haematol. 2003 Feb;120(4):643-51. doi: 10.1046/j.1365-2141.2003.04168.x. Br J Haematol. 2003. PMID: 12588351
Molecular genetics of type 2 von Willebrand disease.
Fressinaud E, Mazurier C, Meyer D. Fressinaud E, et al. Int J Hematol. 2002 Jan;75(1):9-18. doi: 10.1007/BF02981973. Int J Hematol. 2002. PMID: 11843298 Review.
Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII-binding capacity.
Hilbert L, Jorieux S, Proulle V, Favier R, Goudemand J, Parquet A, Meyer D, Fressinaud E, Mazurier C; INSERM Network on Molecular Abnormalities in von Willebrand Disease. Hilbert L, et al. Br J Haematol. 2003 Feb;120(4):627-32. doi: 10.1046/j.1365-2141.2003.04163.x. Br J Haematol. 2003. PMID: 12588349
A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease: A New Epidemiologic Picture.
Veyradier A, Boisseau P, Fressinaud E, Caron C, Ternisien C, Giraud M, Zawadzki C, Trossaert M, Itzhar-Baïkian N, Dreyfus M, d'Oiron R, Borel-Derlon A, Susen S, Bezieau S, Denis CV, Goudemand J; French Reference Center for von Willebrand disease. Veyradier A, et al. Among authors: fressinaud e. Medicine (Baltimore). 2016 Mar;95(11):e3038. doi: 10.1097/MD.0000000000003038. Medicine (Baltimore). 2016. PMID: 26986123 Free PMC article. Clinical Trial.
Mutations in the A3 domain of von Willebrand factor inducing combined qualitative and quantitative defects in the protein.
Legendre P, Navarrete AM, Rayes J, Casari C, Boisseau P, Ternisien C, Caron C, Fressinaud E, Goudemand J, Veyradier A, Denis CV, Lenting PJ, Christophe OD. Legendre P, et al. Among authors: fressinaud e. Blood. 2013 Mar 14;121(11):2135-43. doi: 10.1182/blood-2012-09-456038. Epub 2013 Jan 18. Blood. 2013. PMID: 23335371
A novel ELISA-based diagnosis of acquired von Willebrand disease with increased VWF proteolysis.
Rauch A, Caron C, Vincent F, Jeanpierre E, Ternisien C, Boisseau P, Zawadzki C, Fressinaud E, Borel-Derlon A, Hermoire S, Paris C, Lavenu-Bombled C, Veyradier A, Ung A, Vincentelli A, van Belle E, Lenting PJ, Goudemand J, Susen S. Rauch A, et al. Among authors: fressinaud e. Thromb Haemost. 2016 May 2;115(5):950-9. doi: 10.1160/TH15-08-0638. Epub 2016 Jan 21. Thromb Haemost. 2016. PMID: 26791163
Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide.
Hilbert L, Nurden P, Caron C, Nurden AT, Goudemand J, Meyer D, Fressinaud E, Mazurier C; INSERM Network on Molecular Abnormalities in von Willebrand Disease. Hilbert L, et al. Thromb Haemost. 2006 Sep;96(3):290-4. doi: 10.1160/TH06-03-0157. Thromb Haemost. 2006. PMID: 16953269
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