Basic hemostatic parameters in adults with sickle cell anemia at Ahmadu Bello University Teaching Hospital, Zaria Nigeria

IU Kusfa, SM Aminu, AI Mamman, A Hassan… - Sahel Medical …, 2018 - journals.lww.com
Background: Reports from various studies showed that patients with sickle cell anemia
(SCA) have altered components of hemostasis such as platelet function, the procoagulant …

Sickle cell disease: Assessment of hemostasis parameters in steady-state patients at Tertiary Care Hospital, Indore, India

GK Gupta, PD Sarkar, R Manyal… - … Research Journal (BBRJ …, 2022 - journals.lww.com
Background: The evidence from various studies showed that patients with sickle cell disease
(SCD) have altered components of hemostasis such as platelet function, procoagulant …

[PDF][PDF] Comparative haematological evaluation of sickle cell anaemic patients in steady state and during vaso-occlusive crisis at Maiduguri, Nigeria

UA Abjah, JT Medugu, HA Bulama, IA Nasir… - Nigeria Int J Clin Med …, 2017 - academia.edu
Background: Sickle cell disease (SCD) is a hereditary haemoglobinopathy characterized by
deranged haematopoiesis, and intermittent occlusion of small blood vessels. Patients can …

Haemostatic disorders in sickle cell disease subjects in Nigeria: A review of literature

K Akaba, M Inyama, T Ekwere… - International …, 2018 - research.europeanlibrarypress.com
Background: Sickle cell disease (SCD) is an autosomal recessive disorder that is
characterised with chronic anaemia and painful crisis. SCD is associated with …

Plasma levels of some blood coagulation parameters in Nigerian homozygous sickle cell patients (HbSS) in steady state

FI Buseri, ZA Jeremiah, WA Shokunbi - Hematology, 2006 - Taylor & Francis
The plasma levels of some blood coagulation parameters; prothrombin time,(PT), partial
thromboplastin time with kaolin (PTTK), thrombin clotting time,(TCT), fibrinogen and factor X …

Clinical and biochemical manifestations of severe sickle cell anemia in adult patients in steady state in Ile-Ife, Nigeria

OO Oluwagbenga, DA Ndububa, Y Musah… - Sudan Journal of …, 2019 - ajol.info
Background: There are documented established markers (indices) of disease severity in
patients with sickle cell anemia (SCA) and they determine the course of the disease. This …

Evaluation of von Willebrand factor and other coagulation homeostasis profile of patients with sickle cell anaemia attending a tertiary hospital at Enugu, Nigeria

SO Onoja, BC Eluke, A Dangana, S Musa… - Medical Journal of …, 2020 - mjz.co.zm
Background: Sickle cell anaemia (SCA) is a genetic disorder that has been shown to
facilitate certain forms of coagulopathy. However, there is a paucity of data that …

[HTML][HTML] Coagulation activation in patients with sickle cell disease in Basra, Iraq

WH Saud, MK Hassan, SK Al-Salait - Journal of Applied …, 2017 - journals.lww.com
Background: Sickle cell disease (SCD) is considered to be a hypercoagulable state that
contributes to the morbidity associated with the disease. Numerous mechanisms can …

Haematological values in sickle cell anaemia in steady state and during vaso-occlusive crisis in Benin City, Nigeria

CE Omoti - Annals of African Medicine, 2005 - ajol.info
Background: Sickle cell anaemia (SCA) is a major cause of morbidity and mortality in Africa
where there is no readily available effective treatment. This study was designed to determine …

[PDF][PDF] Hematological Characteristics of a Sample of Iraqi Patients with Sickle Cell Anemia and Their Correlation with Age and Gender

HD Meshay, MH Khamees, HA Wadaha - 2022 - iasj.net
Background: Characterization of hematological parameters in patients with sickle cell
anemia can direct treatment goals toward strategies reducing morbidity and mortality rate …