Results 81 to 90 of about 13,243 (286)

Evaluation of platelet aggregation in splenectomized beta-thalassemia major and intermedia patients

Journal of Applied Hematology, 2018
BACKGROUND: Platelet dysfunction may be one of the pathophysiologic complications in beta-thalassemia patients. However, the results obtained from the platelet aggregation vary in different types of β-thalassemia and among patients.
Mahdi Zahedpanah, Azita Azarkeivan, Minoo Ahmadinejad, Mohamad R Tabatabaiee, Bashir Hajibeigi, Mahtab Maghsudlu   +5 more
doaj   +1 more source

Influence of heart rate variability on platelet hemostasis by average aggregate size in patients with chronic coronary heart disease in combination with COVID-19

Infusion & Chemotherapy
BACKGROUND. In order to prevent complications of coronavirus infection (platelet hemostasis disorders, heart rate variability and QT interval dispersion, which increase the risk of thromboembolic complications and fatal arrhythmias), it is promising to ...
V.Z. Netiazhenko, S.Ye. Mostovyi
doaj   +1 more source

Post‐Diagnosis Hemorrhagic Events Are Strongly Associated With Poor Survival in Patients With Essential Thrombocythemia

eJHaem, Volume 6, Issue 4, August 2025.
ABSTRACT Objectives The present study investigated the effects of thrombosis, hemorrhagic events, disease progression, and secondary malignancies on patient survival after the diagnosis of essential thrombocythemia (ET). Methods We analyzed data from 1152 patients enrolled in the JSH‐MPN‐18 study using time‐dependent Cox regression and multistate ...
Yoshinori Hashimoto, Tomoki Ito, Akihiko Gotoh, Mika Nakamae, Fumihiko Kimura, Michiaki Koike, Keita Kirito, Hideho Wada, Kensuke Usuki, Takayuki Tanaka, Takehiko Mori, Satoshi Wakita, Toshiki I. Saito, Akiko Kada, Akiko M. Saito, Kazuya Shimoda, Yuka Sugimoto, Toshiro Kurokawa, Akihiro Tomita, Yoko Edahiro, Hitoshi Kiyoi, Koichi Akashi, Itaru Matsumura, Katsuto Takenaka, Norio Komatsu   +24 more
wiley   +1 more source

Enhanced Platelet Activity May Increase The Risk of Myocardial Infarction and Stroke in Patients with Chronic Myeloproliferative Neoplasms

Mediterranean Journal of Hematology and Infectious Diseases, 2014
Background. Thrombotic complications may impact mortality and morbidity in chronic myeloproliferative neoplasms (MPNs) mainly polycythemia vera (PV) and essential thrombocythemia (ET).
Viola Maria Popov, Ana Maria Vladareanu, Adrian Tase, Horia Bumbea, Eugenia Kovacs, Camelia Dobrea, Mihaela Georgeta Moisescu, Tudor Savopol, Mihai Popescu   +8 more
doaj  

The Effect of Hyperparathyroid State on Platelet Functions and Bone Loss

Turkish Journal of Hematology, 2016
Objective: Coagulation and fibrinolysis defects were reported in primary hyperparathyroid patients. However, there are not enough data regarding platelet functions in this group of patients.
Göknur Yorulmaz, Aysen Akalın, Olga Meltem Akay, Garip Şahin, Cengiz Bal   +4 more
doaj   +1 more source

Drug-Free Platelets Can Act as Seeds for Aggregate Formation During Antiplatelet Therapy [PDF]

, 2015
The online-only Data Supplement is available with this article at http://atvb.ahajournals.org/lookup/suppl/doi:10.1161/ATVBAHA.115.306219/-/DC1.Medical Research Council, the British Heart Foundation (PG-12-68-29779), the Wellcome Trust (101604/Z/13/Z ...
Abrahamsen AF, Armstrong PC, Cattaneo M, Dassin E, Di Minno G, Ferguson JC, Jneid H, Scott JP   +7 more
core   +1 more source

Anesthesia Management Using Remimazolam in A Patient With Bernard‐Soulier Syndrome: A Case Report

Clinical Case Reports, Volume 13, Issue 5, May 2025.
ABSTRACT Bernard‐Soulier syndrome (BSS) is a platelet dysfunction disorder characterized by massive thrombocytopenia and a lack of platelet aggregation. Remimazolam, a short‐acting benzodiazepine sedative, is believed to have minimal effects on platelets. Here, we report the safe use of remimazolam for anesthesia management in a patient with BSS.
Tomoharu Shakuo, Yusuke Ishida, Daiki Sugawara, Masato Ryo, Haruko Okazaki, Katsunori Oe   +5 more
wiley   +1 more source

Preliminary Study Of Von Willebrand Factor Profiles Of The Different Abo Blood Group Among Malay Population [PDF]

, 2016
Di kalangan 28 juta penduduk Malaysia pada tahun 2010, sebanyak 0.002% pesakit von Willebrand dilaporkan dengan 63% daripadanya berbangsa Melayu.
Abdul Rahman, Rohaida
core  

The contribution of von Willebrand factor-GPIbα interactions to persistent aggregate formation in apheresis platelet concentrates [PDF]

, 2016
BACKGROUND AND OBJECTIVES: Apheresis platelet concentrates sometimes contain persistent aggregates (PA). Because apheresis involves extracorporeal circulation, we hypothesized that interactions between GPIbα and von Willebrand factor (VWF) underlie their
Compernolle, Veerle, Devloo, Rosalie, Feys, Hendrik, Van Aelst, Britt, Vandekerckhove, Philippe   +4 more
core   +2 more sources

Clinical, Phenotypic and Genotypic Characteristics of Von Willebrand Disease in Afro‐Caribbeans: Results From a Study in Martinique Island, French West Indies

Haemophilia, Volume 31, Issue 3, Page 458-476, May 2025.
ABSTRACT Background Several cohort studies have investigated the molecular basis of von Willebrand disease (VWD); very few have focused on the Afro‐Caribbean population. Objectives To determine the genotypic and phenotypic characterization of VWD in a large cohort of Afro‐Caribbean patients living in Martinique.
Marie‐Daniéla Dubois, Olivier Nicolas Pierre‐Louis, Serge Pierre‐Louis, Pierre Boisseau, Cécile V. Denis, Annabelle Dupont, Jenny Goudemand, Caterina Casari, Emmanuelle Jeanpierre, Christophe Zawadzki, Béatrice Ferrey, Johalène Rabout, Pascal Fuseau, Emelyne Chonville, Franck Michel, Marie‐Nadiège Yerro, Yves Gruel, Olivier Christophe, Peter J. Lenting, Eustase Janky, Sophie Susen, Rémi Neviere   +21 more
wiley   +1 more source