A variant of Glanzmann's thrombasthenia with abnormal glycoprotein IIb-IIIa complexes in the platelet membrane.

Alan T. Nurden, Jean‐Philippe Rosa, Dominique J. Fournier, +4

Journal of Clinical Investigation

Intact Platelet MembraneImmunologyMolecular BiologyPlatelet PathobiologyPathology +14

Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII‐binding capacity

Lysiane Hilbert, Sylvie Jorieux, Valérie Proulle, +6

British Journal of Haematology

Total knee arthroplasty in hemophilic arthropathy

Isabelle Legroux-Gérot, Guillaume Strouk, A Parquet, +3

Joint Bone Spine

OsteoarthritisTotal Knee ArthroplastySurgeryJoint ReplacementMusculoskeletal Surgery +3

Transmission of human parvovirus B19 by plasma derived factor VIII concentrates.

Y. Laurian, E Dussaix, A Parquet, +3

PubMed

Viral DiagnosticsViral PathogenesisImmunologyPathologyClotting Factor Concentrate +16

Prevalence of IgG antibodies to human parvovirus B19 in haemophilia children treated with recombinant factor (F)VIII only or with at least one plasma‐derived FVIII or FIX concentrate: results from the French haemophilia cohort

Valérie Gaboulaud, A Parquet, C. Tahiri, +5

British Journal of Haematology

Comparison of Anti-Human and Anti-Porcine Factor VIII Inhibitor Levels in 63 Patients with Severe Haemophilia A

M Fiks-Sigaud, L. Bendelac, A Parquet, +12

Vox Sanguinis

Incidence of Factor IX Inhibitor Development in Severe Haemophilia B Patients Treated with only one Brand of High Purity Plasma Derived Factor IX Concentrate

Y. Laurian, Chantal Rothschild, Robert Navarro, +6

Thrombosis and Haemostasis

Fix InhibitorsImmunohematologyImmunologyGenetic EpidemiologyPathology +14

Hepatitis A in French Hemophiliacs

Jenny Goudemand, A Parquet, Roseline d’Oiron, +8

Vox Sanguinis

Ha ChildrenHepatologyFrench HemophiliacsViral HepatitisMedicine +10

Identification of new type 2B von Willebrand disease mutations: Arg543Gln, Arg545Pro and Arg578Leu

Lysiane Hilbert, Christine Gaucher, J.F. Abgrall, +3

British Journal of Haematology