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Plasma therapy in von Willebrand factor protease deficiency.
Deschênes G, Veyradier A, Cloarec S, Benoit S, Desbois I, Gruel Y, Nivet H. Deschênes G, et al. Among authors: veyradier a. Pediatr Nephrol. 2002 Oct;17(10):867-70. doi: 10.1007/s00467-002-0944-9. Epub 2002 Aug 16. Pediatr Nephrol. 2002. PMID: 12376819
Prothrombin 20210G/A mutation in two patients with mesenteric ischemia.
Balian A, Veyradier A, Naveau S, Wolf M, Montembault S, Giraud V, Borotto E, Henry C, Meyer D, Chaput JC. Balian A, et al. Among authors: veyradier a. Dig Dis Sci. 1999 Sep;44(9):1910-3. doi: 10.1023/a:1018867311839. Dig Dis Sci. 1999. PMID: 10505734
Compound heterozygosity or heterozygosity with two mutations in cis on the same allele? A rebuttal to the letter to the Editors: Koessler et al. Von Willebrand disease caused by compound heterozygosity for p.R854Q and p.R760C: diagnostic and therapeutic implications. Haemophilia 2011; 17: e240-2.
Veyradier A, Fressinaud E, Goudemand J. Veyradier A, et al. Haemophilia. 2011 Sep;17(5):e832-3. doi: 10.1111/j.1365-2516.2011.02531.x. Epub 2011 Apr 13. Haemophilia. 2011. PMID: 21489050 No abstract available.
185 results