Results 121 to 130 of about 13,243 (286)

Identification of 22 novel mutations in patients with Glanzmann's thrombasthenia [PDF]

, 2008
Glanzmann's thrombasthenia (GT) is an autosomal recessive inherited platelet function defect that characterized by reduction in, or absence of, platelet aggregation in response to multiple physiologic agonists. GT is characterized by normal platelet
Abdul Ethayathulla, Birendra Yadav, Firdos Ahmad, Meganathan Kannan, Rajive Kumar, Renu Saxena, Ved Choudhry   +6 more
core   +1 more source

Effects of Modification of the Platelet Surface on Receptors for Aggregated IgG and Ristocetin-Von Willebrand Factor [PDF]

, 1977
Sharron L. Pfueller, C. S. P. Jenkins, E. F. Lüscher   +2 more
openalex   +1 more source

PO09 | Comparison of different aggregometry methods for evaluation of platelet function in patients with myeloproliferative neoplasms

Bleeding, Thrombosis and Vascular Biology
Background and Aims: Myeloproliferative neoplasms (MPN) are clonal disorders of hematopoietic stem cells characterized by increased thrombotic and hemorrhagic complications.
doaj   +1 more source

Poster Sessions

HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source

Increased von Willebrand Factor and Defective Ristocetin-Induced platelet Aggregation in Liver Disease [PDF]

, 1977
S Maragall, Antonio Ordinas, Carmine Clemente, F Casals, J. Profitós, R. Castillo   +5 more
openalex   +1 more source

Single-platelet nanomechanics measured by high-throughput cytometry [PDF]

, 2016
Ahn, B., Baek, J., Bennett, C., Briones, M., Brown, A. C., Bunting, S., Chester, D., Ciciliano, J., Ciciliano, J., Cuadrado, J., Fay, M. E., Fernandez-Nieves, A., Lam, W. A., Mannino, R., Myers, D. R., Qiu, Y., Sakurai, Y., Smith, Michael L., Sulchek, T., Tennenbaum, M., Tran, R.   +20 more
core   +2 more sources

Molar substitution and C2/C6 ratio of hydroxyethyl starch: influence on blood coagulation [PDF]

, 2017
Background. Development of hydroxyethyl starches (HES) with a low impact on blood coagulation but a long intravascular persistence is of clinical interest.
Bombeli, T., Burmeister, M.-A, Fisch, A., Frascarolo, P., Madjdpour, C., Schramm, S., Spahn, D. R., von Roten, I.   +7 more
core  

Publication Only

HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source

von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma [PDF]

, 1986
Lars Holmberg, Erik Berntorp, Mikael Donnér, Nilsson Im   +3 more
openalex   +1 more source

Bernard-Soulier syndrome: a flow cytometric analysis of membrane GP-Ib expression

The Turkish Journal of Pediatrics, 1996
A case of Bernard-Soulier syndrome in a five-year-old female is presented. The diagnosis was confirmed by flow cytometric analysis of glycoprotein Ib (CD 42b) in addition to the patient's classic laboratory findings such as prolonged bleeding time,
M A Yeşilipek, I Karadoğan, L Undar
doaj