Eminent Editorial Board Members
In the worldwide due to Blood disorders, millions of people are facing the significant number of deaths. The treatments for some of the disorders do exist, but many of the blood disorders are incurable, chronically or receiving symptomatic treatment. Scientists are conducting the research to treat these disorders and to eradicate this type of diseases completely.
Journal of Blood Disorders and Therapeutics (JBDT) emphases to publish original research papers, reviews, perspectives, rapid communication, short communications, mini-reviews, and commentaries, in the relative fields including diagnosis, prevention, treatment of Hematological disorders.
RECENT ARTICLES
Assessment of Clinical Blood Transfusion Practice in a Pediatric Tertiary Hospital in Cameroon
Yearly, 112.5 million blood donations are collected globally with half of these done in the high income countries. In Cameroon, 400,000 bags of blood are needed every year for the treatment of patients in hospitals. The World Health Organisation (WHO...
Do Fibrinogen Levels Serve as Indicator of Hepatic Iron Overload in Patients with High Transfusion Regimes Due to a Hematologic Disease?
Despite some major improvements in treating beta thalassemia in the past, it remains a challenge to avoid the various complications which go along with iron overload. We retrospectively analyzed data from 17 patients with transfusion-dependent anemia...
Acute Unfavourable Transfusion Outcomes in Children: Frequency and Pattern in Resource Limited Settings
Unfavourable transfusion outcomes (UTOs) compromise the efficiency and safety of blood transfusion in sub-Saharan Africa burdened by financial inaccessibility to advanced transfusion reaction prophylaxis. To provide less sophisticated solutions, it i...
Haploidentical Bone Marrow Transplant with Treosulfan- Fludarabine- TBI conditioning in Pediatric Familial HLH with Compound Heterozygote STXBP2 Mutation- A Case Report and Review of Literature
Familial hempophagocytic lymphohistiocytosis (FHLH) is a rare life threatening hyperinflammatory clinical syndrome requiring a high level of clinical suspicion for rapid and appropriate diagnosis and appropriate management. STXBP2 gene mutation or FH...
Prevalence and Associated Factors among Pregnant Women with Anemia Attending Al-Thawra Hospital, Sana’a City, Yemen
The occurrence of anemia during pregnancy is usually associated with an increased risk of maternal, fetal, and newborn morbidity and mortality, particularly in low-income countries like Yemen. This study, therefore, aimed to assess prevalence and fac...
Study of the Anti-Anemic Activity of the Aqueous Extract of the Leaves of Petroselinum Crispum (Apiaceae) In the White Mouse (Mus Musculus) Of SWISS Strain
Petroselinum crispum (parsley) is a plant well known and much appreciated by African populations in general and Ivorians in particular. It is used for its anti-oxidant, antimicrobial, anti-diabetic, cardiovascular, anti-cancer and gastrointestinal pr...
Diffuse Large B-cell Lymphoma Circulating at Diagnosis
We present a case of Diffuse Large B-cell Lymphoma whose initial presentation was in the leukemic form. This is a rare presentation, whose morphological analysis is difficult and immunophenotyping by flow cytometry played an important role in the dia...
Biochemical Response to Vasoclusive Crisis in Sickle Cell Anemia Patients in Enugu South East, Nigeria
Biochemical response to vascoclusive crisis were investigated among Sickle Cell Anemia (SCA) patients in Enugu metropolis,
Southeast Nigeria. A total of 156 subjects comprising 75 confirmed SCA patients (35 males and 40 females) aged between
16 and...
