Results 81 to 90 of about 9,310 (270)

Enhanced platelet adhesion in essential thrombocythemia after in vitro activation [PDF]

, 2010
Objective: Essential thrombocythemia (ET) is a chronic myeloproliferative disorder characterized by elevated platelet counts and increased risk of thrombosis.
Andreas C. Eriksson, Kourosh Lotfi, Per A. Whiss   +2 more
core  

Complications at Diagnosis of Pediatric Chronic Myeloid Leukemia in Chronic Phase

Pediatric Blood &Cancer, Volume 72, Issue 10, October 2025.
ABSTRACT Chronic myeloid leukemia (CML) is uncommon during the first two decades of life, resulting in limited experience of pediatricians in handling this leukemia. This is even more true when it comes to managing rare complications at the time of diagnosis.
Nirmalya Roy Moulik, Uma Athale, Markus Metzler, Frederic Millot, Meinolf Suttorp   +4 more
wiley   +1 more source

Diagnostic tool for Glanzmann\u27s thrombasthenia clinicopathologic spectrum [PDF]

, 2008
OBJECTIVE: To platelet aggregometry and describe the clinical spectrum of Glanzmann\u27s thrombasthenia diagnosed by platelet aggregometry. STUDY DESIGN: A case-series.
Adil, Salman, Ali, Natasha, Moiz, Bushra, Rahman, Yasmeen, Rizvi, Bushra, Shaikh, Usman   +5 more
core   +1 more source

von Willebrand's disease: a report from a meeting in the Åland islands [PDF]

, 2012
von Willebrand's disease (VWD) is probably the most common bleeding disorder, with some studies indicating that up to 1% of the population may have the condition.
Bergamaschini, Berntorp, Berntorp, Berntorp, Berntorp, Berntorp, Borel-Derlon, Bowen, Dean, Dunkley, Federici, Federici, Flood, Franchini, Goodeve, Hyatt, Iorio, Klenk, Laffan, Larsson, Lassila, Lethagen, Mannucci, Mannucci, Matsui, McGrath, Nichols, Nilsson, Pasi, Rodeghiero, Rodeghiero, Ruggeri, Ruggeri, Sadler, Sadler, Sarji, Soulier, Stray-Pedersen, Sweeney, Titani, Tosetto, Von Willebrand, Von Willebrand, Von Willebrand, Williams, Witmer, Zhang   +46 more
core   +1 more source

Bleeding Complications in JAK2‐Variant Essential Thrombocythemia: A Revisit in 2025

eJHaem, Volume 6, Issue 4, August 2025.
ABSTRACT Essential thrombocythemia (ET) is a myeloproliferative neoplasm characterised by sustained thrombocytosis. Paradoxically, bleeding complications remain an under‐recognised clinical challenge. Compared with CALR‐mutated patients, those harbouring the JAK2‐V617F variant appear more prone to haemorrhage.
Gerard Gurumurthy, Samantha Gurumurthy, Tim C. P. Somervaille, Anna Falanga, Jecko Thachil   +4 more
wiley   +1 more source

The relationship between ABO groups and subgroups, factor VIII and von Willebrand factor

Haematologica, 2007
The aim of this study was to correlate ABO groups with plasma levels of factor VIII (FVIII), von Willebrand factor (VWF:Ag), and ristocetin cofactor (VWF:RCo).
Norma Cristina Sousa, Joyce Maria Anicchino-Bizzacchi, Maria Fátima Locatelli, Vagner Castro, Maria Lourdes Barjas-Castro   +4 more
doaj   +1 more source

Comparison of the adsorption dynamics of leucyl-leucine enantiomers and glycyl-glycine on Chirobiotic R and Chirobiotic V columns

Journal of Chromatography Open
The adsorption dynamics of the LL- and DD-enantiomers of Leu-Leu and Gly-Gly on a Chirobiotic V column packed with a CSP bearing glycopeptide antibiotic vancomycin was studied and compared with the adsorption dynamics of the same dipeptides on a ...
Yana A. Klimova, Leonid D. Asnin
doaj   +1 more source

Our First Experience with Magnetic Separation of Platelets for Analyses of Platelet MicroRNA in Patients with Sticky Platelet Syndrome

Acta Medica Martiniana, 2019
Introduction: Sticky platelet syndrome (SPS) is referred to as a platelet hyperaggregability triggered by low concentrations of platelet agonists adenosine diphosphate (ADP) and/or epinephrine (EPI).
Vadelova L, Ivankova J, Sokol J, Skerenova M, Zolkova J, Vazanova A, Skornova I, Stasko J   +7 more
doaj   +1 more source

The N-terminal domain of human GATA1 prevents dyserythropoietic anemia and megakaryocyte dysplasia in vivo [PDF]

, 2015
We describe a child with dyserythropoietic anemia, thrombocytosis, functional platelet defect, and megakaryocyte dysplasia. We show that (i) this constellation of hematopoietic abnormalities was due to a germline mutation within the 5′ untranslated ...
Czader, Magdalena, Nalepa, Grzegorz, Temm, Constance, Zucker, Jacob   +3 more
core   +2 more sources

Identification of one novel pathogenic ITGB3 mutation and two known mutations in two Chinese pedigrees with hereditary Glanzmann thrombasthenia

Platelets, 2020
Glanzmann thrombasthenia (GT) is an inherited disorder of platelet aggregation resulting from quantitative and/or qualitative abnormalities of the glycoprotein IIb/IIIa complex.
Zhengjing Lu, Lauriane Nikuze, Zhoulin Zhong, Fang Li, Fuyong Zhang, Kairong Liang, Manlv Wei, Hongying Wei   +7 more
doaj   +1 more source