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Platelets|January 19, 2002
Description of 10 new mutations in platelet glycoprotein IIb (alphaIIb) and glycoprotein IIIa (beta3) genesC Vinciguerra, J C Bordet, G Beaune, et al.
Revue Du Rhumatisme (English Ed.)|October 1, 1995
Predictors of the need for total hip replacement in patients with osteoarthritis of the hipC Vinciguerra, A Gueguen, M Revel, et al.
British Journal of Haematology|February 5, 1998
Illegitimate transcription: its use for studying genetic abnormalities in lymphoblastoid cells from patients with Glanzmann thrombastheniaC Negrier, C Vinciguerra, O Attali, et al.
Scientific Reports|June 11, 2026
Utilizing 45 years of instrumental seismicity to investigate blind seismogenic faults in Southeastern PiedmontFrancisca Guiñez-Rivas, Sergio C Vinciguerra, Cesare Comina, et al.
Revue Neurologique|July 13, 2000
[Postoperative combined medullary sclerosis revealing Biermer's disease: toxic effect of nitrous oxide]C Vinciguerra, P Chazerain, J P Olivero de Rubiana, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 27, 2016
Characterization of five associations of F8 missense mutations containing FVIII B domain mutationsY Jourdy, C Nougier, O Roualdes, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 25, 2015
Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiencyO Roualdes, C Nougier, M Fretigny, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 31, 2013
Characterization of four novel molecular changes in the promoter region of the factor VIII geneC Nougier, O Roualdes, M Fretigny, et al.
Thrombosis and Haemostasis|September 1, 1995
Molecular study of Glanzmann thrombasthenia in 3 patients issued from 2 different familiesC Vinciguerra, M C Trzeciak, N Philippe, et al.
Journal of Thrombosis and Haemostasis : JTH|June 29, 2004
Two novel mutations in EGF-like domains of human factor IX dramatically impair intracellular processing and secretionN Enjolras, J-L Plantier, M-H Rodriguez, et al.
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