Results 181 to 190 of about 13,399 (295)

Use of the collagen‐binding assay for von Willebrand factor 
in the analysis of type 2M von Willebrand disease: 
a comparison with the ristocetin cofactor assay [PDF]

, 2002
Anne Riddell, P. Vincent Jenkins, Ioana Nitu-Whalley, A. McCraw, Christine A. Lee, Simon Brown   +5 more
openalex   +1 more source

Acquired Bernard-Soulier-like syndrome due to a plasma-based inhibitor treated successfully with rituximab. [PDF]

Res Pract Thromb Haemost
Banaszak LG, Clark PA, Peterson CG, Sheehan J.   +3 more
europepmc   +1 more source

The Effects of Ristocetin and von Willebrand Factor on Platelet Electrophoretic Mobility [PDF]

, 1978
Barry S. Coller
openalex   +1 more source

Oscillatory Response of Ristocetin Induced-Platelet Aggregation in Thrombasthenia [PDF]

, 1977
Juan Chediak, Margaret Telfer, B. Vander Laan, Isaac Cohen   +3 more
openalex   +1 more source

Defective ristocetin-induced platelet aggregation in von Willebrand's disease and its correction by factor VIII.

Journal of Clinical Investigation, 1973
H. Weiss, J. Rogers, H. Brand
semanticscholar   +1 more source

Recurrent Intramuscular Hematoma Revealing Moderate Congenital Factor XIII Deficiency. [PDF]

Cureus
Ben Halima N, Riahi S, Mazlout I, Mgarrech I, Bouatay A.   +4 more
europepmc   +1 more source

Total Laparoscopic Hysterectomy in Factor XI Deficiency: A Case Report. [PDF]

Cureus
Ortiz-Villanueva BJ, Lopez-Chavez AG, Mendoza-Torres A, Bravo-Rodriguez LM, Interián-Alvarez FJ.   +4 more
europepmc   +1 more source

Acquired von Willebrand syndrome in young children with congenital heart defects: focus on patent ductus arteriosus and ventricular septal defect. [PDF]

Res Pract Thromb Haemost
Trębacz O, Szafarz K, Zdziarska J, Podlewski J, Weryński P, Tarała W, Iwaniec T.   +6 more
europepmc   +1 more source

Acquired Bernard-Soulier syndrome as the presenting feature of GATA2-related myeloid neoplasm in an adolescent: an insight into the mechanisms underlying the platelet defect. [PDF]

Haematologica
Kamiya LJ, Morell MD, Marta RF, Narbaitz M, Marzac C, Goette NP, De Luca G, Lev PR, Metrebian MF, Ganiewich D, Llera AS, Raslova H, Heller PG, Glembotsky AC.   +13 more
europepmc   +1 more source

von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib.

Proceedings of the National Academy of Sciences of the United States of America, 1992
I. Rabinowitz, E. Tuley, D. Mancuso, A. Randi, B. Firkin, M. Howard, J. Sadler   +6 more
semanticscholar   +1 more source