M. Morsed Zaman Miah Automated reticulocyte counts are widely used in the clinical laboratory due to their greater precision, accuracy and reproducibility compared to those obtained using the microscope. Automated methods employ a wide variety of reagents for reticulocyte RNA … Continue reading →
Farida Parvin, Bepasha Naznin, Tamanna Afroz, Tashmim Farhana Dipta, Salma Afrose Background: Plateletpheresis is the process in which healthy donor blood is passed through an apparatus that separates out platelets and returns the remainders to the circulation. As the demand … Continue reading →
Tashmim Farhana Dipta, Amin Lutful Kabir, Mohammed Abdul Quader, Manjuma Rahman, Farida Parvin, Masuda Begum, Ayesha Khatun, Jolly Biswas, Salma Afrose To our knowledge, this is the first reported case from Bangladesh of a 27-year-old-young man having ‘E-Beta thalassaemia’ along … Continue reading →
Mamun Al Mahtab, Md. Abdur Rahim, Sheikh Mohammad Noor-E-Alam, Ashraful Alam, Faiz Ahmad Khondokar, Ahmed Lutful Moben Introduction: Decompensated cirrhosis of liver is associated with decreased amounts of functional hepatocytes leading to compromised quality of life and increased mortality; Liver … Continue reading →
Dilshad Jahan Graft failure is a significant complication following allogeneic hematopoietic cell transplantation (AHCT). It may be due to rejection caused by recipient T-cells, NK-cells or antibodies. It is increased in HLA-mismatched grafts, unrelated grafts, T-cell replete transplants, sensitized patients … Continue reading →
Abu Jafar Mohammed Saleh Hematopoietic stem cell transplantation (HSCT) is a lifesaving, costly, and multistep procedure. It took more than 50 years from the first published attempt in 1957 to arrive at one million transplants by 2012 and currently more … Continue reading →
Mizanur Rahman, Rummana Rahim, Abu Hasan Paroxysmal nocturnal haemoglobinuria (PNH) is a rare stem cell disorder caused by acquired mutation in the X-linked phosphatidylinositol glycan complementation class A gene. The acquired mutation generates a defect in the expression of glycol-phosphatidyl … Continue reading →
Quazi Smita Haq, Dilsad Jahan, Muhammad Sahidul Islam Sikder, Muhammad Sazzad Zayed Chowdhury, Masba Uddin Chowdhury, Md Maruf Al Hasan, Abu Jafar Mohammed Saleh Background: Diamond-Blackfan anaemia is a rare congenital red blood cell aplasia characterized by failure of erythropoiesis, … Continue reading →
Background: AML is heterogeneous in terms of morphology, immunophenotype, cytogenetics and molecular genetics. Cytogenetic analysis performed at diagnosis is considered to be the most important prognostic factor in AML. The cytogenetic pattern of AML in Bangladeshi population is not clearly … Continue reading →
Background: Acute leukaemia (AL) are a heterogenous group of haematological malignancy characterized by uncontrolled clonal proliferation of haematopoietic progenitor cells. The study was conducted to have a detailed understanding of immunophenotyping profile, the frequency of discrepancy between bone marrow morphology … Continue reading →
