[HTML][HTML] A comparative study of D-dimer levels in adult patients with sickle cell anemia at Ahmadu Bello University Teaching Hospital Zaria, Nigeria

IU Kusfa, AI Mamman, AA Babadoko… - Nigerian Journal of …, 2017 - journals.lww.com
Objectives: To determine the D-dimer levels and some hematological parameters of adult
patients with sickle cell anemia in steady state attending the hematology clinic of Ahmadu …

Elevated Plasma D-dimer Levels In Children with Sickle Cell Anemia In Steady State Attending State Specialist Hospital Maiduguri, Borno State, Nigeria

SA Ibrahim, IG Mukhtar, AB Mohammed… - Nigerian Journal of …, 2020 - ajol.info
Background: Sickle cell anemia (SCA) has been linked with altered plasma levels of D‑
dimer. However, routine assessment of D‑dimer and other coagulation indices in SCA …

[PDF][PDF] Haemostatic changes in patients with sickle cell disease in steady state and in vaso-occlusive crises

SG Ahmed, UA Ibrahim, BA Umar - Nigerian Journal of, 2000 - researchgate.net
Background: The platelet count, prothrombin time (PT), activated partial thromboplastin time
(APTT) and D-dimer levels of patients with sickle cell disease (SCD) in steady state (32 …

[PDF][PDF] Determination of D-dimer level in sickle cell anemia patients under hydroxyurea treatment in Sinnar state, Sudan

EA Fadelmula, MHA Abdalla - GSC Biological and …, 2020 - gsconlinepress.com
Sickle cell disease (SCD) is a group of blood disorders typically inherited from a person's
parents. The most common type is known as sickle cell anemia (SCA), is hemoglobin …

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 …

[PDF][PDF] Investigate of Haemostatic and Fibrinolytic System Parameters among Sickle Cell Anaemia Patients in the Khartoum State

EG Elnaim, S Ibrahim, D Ahmed, R Aldaw, N Salih… - Indian J …, 2020 - academia.edu
Introduction: A sickle cell anaemia one of a haemoglobinopathy, which constituted as a
model for genetically inherited disorders, the course of the disease involves may crises, the …

[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 …

DD dimer levels in patients with sickle cell disease during bone pain crises and in the steady state

EE Fakunle, K Iwara Ibiang Eteng… - Pathology and …, 2012 - Taylor & Francis
Objective: To determine the presence of ongoing thrombosis by measuring the DD dimer
levels in bone pain crises (BPCs) and in the steady state of patients with sickle cell disease …

Haematological parameters of adult and paediatric subjects with sickle cell disease in steady state, in Benin City, Nigeria

OE Iheanacho - International Blood Research & Reviews, 2015 - archive.pcbmb.org
Background: Sickle cell disease (SCD) remains a major health burden in Sub-Saharan
Africa and the management requires regular monitoring of the patients. The monitoring …

Complement Levels in Nigeria Patients with Sickle Cell Anaemia in the Asymptomatic State

TI Okeke, BOP Musa, AA Babadoko… - Nigerian Journal of Clinical …, 2018 - ajol.info
Objectives: Significantly low serum levels of complement components have been reported in
patients with Sickle cell anaemia (SCA) which may result in a high susceptibility to …