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Asian Hematology Research Journal

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281

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56

2026 articles

281

Open access

6

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Articles (281)

A Comparison of Two HIV Antibody ELISAs with a Combined Antigen-Antibody ELISA for the Occurrence of False Results in a Hospital-Based Blood Bank In north-Central Nigeria: Implications on Blood Safety and Availability

Joseph Aondowase Orkuma, Julie Ochaka Egesie, Simji Samuel Gomerep & Ejele Osaikhuemen Adebayo · Asian Hematology Research Journal · 2018

Background: Global targets of providing safe blood available universally by 2020 as well as that seeking to eliminate HIV transmission by 2030 has compelled many hospital-based blood banks to employ relevant strategies in their transfusion practice towards realizing these targets...

Open access Research Article

Evaluation of von Willebrand Factor Levels in Sickle Cell Patients Attending Babcock University Teaching Hospital

A. O. Olayanju Dickson, E. D. Ezigbo, Erukpeme Augusta & Okeke Chinwe · Asian Hematology Research Journal · 2018

Introduction: von Willebrand Factor (VWF) plays a vital role in platelet aggregation. The unusually large VWF multimers mediate the adhesion of sickle red blood cell (RBC) to endothelial cells and contribute to vaso-occlusive episodes. Objective: The aim of this study was to dete...

Open access Research Article

Non-Fasting Total Serum Homocysteine (tHcy) Levels in Folate-Supplemented Omani Arabs with Sickle Cell Disease in the Steady State and in Crisis

Huxley Knox-Macaulay, David Gravell, Gavin Ross, Fehmida Zia, Anil Pathare & Salam Al Kindi · Asian Hematology Research Journal · 2018

The aim of this investigation is to determine tHcy levels in SCD Omani Arabs in (i) the steady state (ii) crisis (iii) relative to non-SCD subjects as such values might help clarify the role of tHcy in SCD.  Serum tHcy concentrations and other laboratory analyses including serum...

Open access Research Article

Clinical and Biologic Outcomes Following the Administration of Hydroxyurea to Homozygote Sickle Cell Patients in Two Health Facilities of Yaounde

B. Chetcha Chemegni, A. V. Kouam Kaping, I. Ngosso Tetanyé, A. Bodieu Kenmegne, L. Kouemeni, G. Ngouefo, E. K. Ola Bamzok, Tetanye Ekoe & L. Kaptué Noche · Asian Hematology Research Journal · 2018

Sickle cell disease is the most frequent genetic disease worldwide with high mortality and morbidity rates. Several therapeutic medications have been put in place amongst which hydroxurea, an antineoplastic for which the clinical-biologic benefits for the patients have been estab...

Open access Research Article

Histomorphological and Thrombogenic Status of Wistar Rats Fed with Allium sativum (GARLIC) in Oxidative Stress Induced with Carbon Tetrachloride

I. K. Aromose, M. O. Ebeye, I. T. Ekwere, M. O. Odigie, P. R. C. Esegbue & J. C. Igweh · Asian Hematology Research Journal · 2018

Though concerns over the safety of medicinal drugs are following rife consumption of some herbal preparations, the underlying pathogenesis remains however cryptic. Awareness of the far-reaching effects of herbal preparations is germane to their continued use in traditional medici...

Open access Research Article

Validation Hematological Analyzer for Assay of Erythrogram in Hodeidah City, Yemen

Saeed Al-Sheibani, Salma Osman Taha, Fuad Balkam, Adel Dhfash & Mohammed Amood Al-Kamarany · Asian Hematology Research Journal · 2018

The hematological indices namely erythrogram is an important parameter for evaluating human’s physiological status. I can vary accordingly depending upon the differential traits (Asian, Arabian, European … etc), sex, age, and health condition. In best of our knowledge, due to lac...

Open access Research Article

Protein-energy Status and Oxidative Stress of a Group of Patients with Sickle Cell Disease in Yaoundé - Cameroon: Effect of Some Intrinsic and Extrinsic Factors

Nya Nkwikeu Prudence Josela, Biapa Nya Prosper Cabral, Chetcha Bernard, Yembeau Lena Natacha, Kengne Fotsing Christian Bernard & Pieme Constant Anatole · Asian Hematology Research Journal · 2018

Background: SCA is a systemic disease which affects more than 50 million people in the world. The gene mutation results in the cause of the synthesis of abnormal haemoglobin S (HbS) which is a pro-oxidant machine and induces ROS production. In addition, sickle cell patients are d...

Open access Research Article

Electrolytic and Oxidative Stress Profile of Sickle Cell Anaemia Patients in Cameroon: The Effect of Some Extrinsic Factors

Kengne Fotsing Christian Bernard, Biapa Nya Prosper Cabral, Chetcha Bernard, Nguelewou Lemlon Flora, Pieme Constant Anatole & Gatsing Donatien · Asian Hematology Research Journal · 2018

Sickle cell anaemia is a hereditary blood disease characterized by the presence of haemoglobin S in red blood cells. It affects over 2 million people in Cameroon. Haemoglobin S can induce the oxidative stress and changes in electrolyte level in patients. The aim of this study was...

Open access Research Article

The Value of Red Blood Cell Indices in the Diagnosis of Severe Malaria at a Tertiary Hospital in North-Eastern Nigeria

Iragbogie Al-Mustapha Imoudu, Hayatu Ahmad, Maimuna O. Yusuf & Hauwa U. Makarfi · Asian Hematology Research Journal · 2018

Aim: This study aimed at evaluating the red cell indices of children seen at the Federal Medical Centre, Azare, Nigeria, with a view to determining their utility in the diagnosis of severe malaria. Study Design: The study was a case control study. Place and Duration of the study:...

Open access Research Article