Results 111 to 120 of about 13,243 (286)

Macrotrombocitopenia isolada crónica hereditária - estudo de uma família Portuguesa [PDF]

, 2003
Apresenta-se uma família com macrotrombocitopenia hereditária crónica (MHC) documentada em 6 elementos pertencentes a 3 gerações. A propositus era uma criança com 7 anos de idade, enviada a Consulta de Hematologia por trombocitopenia moderada (90 X ...
Antunes, Marika Bini, Barbot, José, Costa, Elísio, Morais, Sara   +3 more
core  

High shear induces platelet dysfunction leading to enhanced thrombotic propensity and diminished hemostatic capacity

Platelets, 2019
Thrombosis and bleeding are devastating adverse events in patients supported with blood-contacting medical devices (BCMDs). In this study, we delineated that high non-physiological shear stress (NPSS) caused platelet dysfunction that may contribute to ...
Zengsheng Chen, Nandan K. Mondal, Shirong Zheng, Steven C. Koenig, Mark S. Slaughter, Bartley P. Griffith, Zhongjun J. Wu   +6 more
doaj   +1 more source

Coagulation factors in spray‐dried plasma: A systematic review and meta‐analysis

Transfusion, Volume 65, Issue 5, Page 1012-1020, May 2025.
Biswadev Mitra, Patrick J. C. Biggins, Denese C. Marks, Michael C. Reade   +3 more
wiley   +1 more source

LABRAD : Vol 32, Issue 1 - January 2007 [PDF]

, 2007
T-Cell Receptor (TcR) Gene Rearrangement Studies: A Useful Adjunct for the Diagnosis of T-Cell Lymphoproliferative Disorders Vitamin D Measurement Quiz Ristocetin Cofactor Activity Portal Biliopathy- An Uncommon Cause of Biliary Obstruction Laboratory ...
Aga Khan University Hospital, Karachi
core   +1 more source

The specificity of combination between ristocetins and peptides related to bacterial cell wall mucopeptide precursors [PDF]

, 1971
M. Ángela Nieto, H. R. Perkins
openalex   +1 more source

Novel point mutation in a leucine-rich repeat of the GPIbα chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant

Haematologica, 2008
In Italy, a significant proportion of patients with autosomal dominant inheritance of macrothrombocytopenia have been recognized as having heterozygous Bernard-Soulier syndrome carrying the Bolzano-type defect. This condition prompted a systematic review
Silvia Vettore, Raffaella Scandellari, Stefano Moro, Anna Maria Lombardi, Margherita Scapin, Maria Luigia Randi, Fabrizio Fabris   +6 more
doaj   +1 more source

LABRAD : Vol 38, Issue 1 - July 2012 [PDF]

, 2012
How to Investigate a Bleeding Disorder Nucleic Acid Testing at AKUH Lab Diagnosis of von Willebrand Disease Scoring Systems in Diagnosis of Disseminated Intravascular Coagulation Plasma and Platelet Transfusions in Liver Diseases Ristocetin Cofactor ...
Aga Khan University Hospital, Karachi
core   +1 more source

Autosomal dominant macrothrombocytopenia caused by a rare GPIBB variant : the importance of DNA sequencing [PDF]

, 2020
De Kesel, Pieter, Debussche, Sarah, Devreese, Katrien, Dierick, Jan, Freson, Kathleen, Luyckx, Ariane, Vantilborgh, Anna   +6 more
core   +2 more sources

Abnormalities of factor VIII and platelet aggregation--use of ristocetin in diagnosing the von Willebrand syndrome [PDF]

, 1975
HJ Weiss
openalex   +1 more source

Von Willebrand's disease: case report and review of literature

The Pan African Medical Journal, 2017
Von Willebrand Disease (VWD) is the most common human inherited bleeding disorder due to a defect of Von Willebrand Factor (VWF), which a glycoprotein crucial for platelet adhesion to the subendothelium after vascular injury.
Hanae Echahdi, Brahim El Hasbaoui, Mohamed El Khorassani, Aomar Agadr, Mohamed Khattab   +4 more
doaj   +1 more source