Comparison of von Willebrand Disease and Bernard-Soulier Syndrome

Thromb Haemost 1977; 38(02): 0586-0587
DOI: 10.1055/s-0038-1651868

Letters to the Editor

Schattauer GmbH

Authors

J. P Caen

¹Research unit INSERM 150, Hopital Saint-Louis, 2 Place du Dr. Fournier, Paris
H Michel

¹Research unit INSERM 150, Hopital Saint-Louis, 2 Place du Dr. Fournier, Paris
Y Sultan

¹Research unit INSERM 150, Hopital Saint-Louis, 2 Place du Dr. Fournier, Paris
G Tobelem

¹Research unit INSERM 150, Hopital Saint-Louis, 2 Place du Dr. Fournier, Paris
A. T Nurden

¹Research unit INSERM 150, Hopital Saint-Louis, 2 Place du Dr. Fournier, Paris
S Levy-Toledano

¹Research unit INSERM 150, Hopital Saint-Louis, 2 Place du Dr. Fournier, Paris

References
1 Caen J. P, Nurden A. T, Jeanneau C, Michel H, Tobelem G, Levy-Toledano S, Sultan Y, Valensi F, Bernard J. 1976; Bernard-Soulier syndrome: A new platelet glycoprotein abnormality. Its relation to platelet adhesion to subendothelium and with the factor VIII von Willebrand protein. Journal of Laboratory and Clinical Medicine 87: 586.
2 Caen J. P, Michel H, Tobelem G, Bodevin E, Levy-Toledano S. 1977; Adhesion and aggregation of human platelets to rabbit subendothelium. A new approach for investigation: specific antibodies. Experientia 33: 91.
3 O’Brien J. R, Heywood J. B. 1967; Some interactions between human platelets and glass: von Willebrand’s disease compared with normal. Journal of Clinical Pathology 20: 56.
4 Tobelem G, Levy-Toledano S, Bredoux R, Degos L, Michel H, Nurden A, Caen J. P. 1976; New approach to determination of specific functions of platelet membrane sites. Nature 263: 427.