↓
 
Haematology Society of Bangladesh

Haematology Society of Bangladesh

The Representative Organization of All Haematologists in Bangladesh

  • HOME
  • ABOUT US
    • OVERVIEW
    • CONSTITUTION
    • EXECUTIVE COMMITTEE
    • MEMBERSHIP
      • ABOUT MEMBERSHIP
      • MEMBERS’ DIRECTORY
        • LIFE MEMBERS
        • LIFE MEMBER (HONOURARY)
        • GENERAL MEMBERS
        • ASSOCIATE MEMBERS
        • LIFE MEMBERS (LATE )
    • CONTACT US
  • JOURNAL
  • RESOURCE
    • DISCUSSION/NOTES
    • GUIDELINES AND PROTOCOLS
      • BRITISH HAEMATOLOGY GUIDELINE
      • EHA CLINICAL PRACTICE GUIDELINE
      • NCCN GUIDELINES
      • PROTOCOLS AND GUIDELINES
  • LABORATORY SERVICES
  • PATIENTS’ CORNER
    • FIND A HAEMATOLOGIST
    • FIND A HAEMATOLOGY CENTRE
    • PATIENTS’ GUIDELINES
    • FREQUENTLY ASKED QUESTIONS
  • Election 2023
Log in

Post navigation

<< 1 2 … 5 6 7 8 9 10 11 … 16 17 >>

Splenectomy in Thalassaemia: Why, When and How

Haematology Society of Bangladesh

Shahnoor Islam Splenectomy is indicated in the transfusion-dependent thalassaemia patient when increased blood transfusion requirement that prevents adequate control with iron chelation therapy, hypersplenism, symptomatic splenomegaly. Annual transfusion volume exceeding 225 to 250 mL/kg/year with packed red blood cells may … Continue reading →

Measurement of Bone Mineral Density in the Transfusion Dependent Thalassaemic Patients

Haematology Society of Bangladesh

Showrab Biswas, Md. Salahuddin Shah, Md. Abdul Aziz, Md Rafiquzzaman Khan, Masuda Begum, Fatima Begum, Surozit Kumar Sarkar, Saqi Md. Abdul Baqi  Background: Thalassaemia causes a lot of complications. Among them low bone mineral density represents a major cause of … Continue reading →

Newer Reticulocyte Parameters: Hope for Diagnosis & monitoring of Anaemia

Haematology Society of Bangladesh

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 →

A Multicentre Study on The Causes and Frequency of Donor Deferral Along with Adverse Reaction During Plateletpheresis

Haematology Society of Bangladesh

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 →

Para-Bombay Blood Phenotype with E-Beta Thalassaemia: A Rarest Case Report from Bangladesh

Haematology Society of Bangladesh

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 →

Autologous Haemopoietic Stem Cell Transplantation in Decompensated Cirrhotics Via Portal Venous Route – Initial Experience from Bangladesh

Haematology Society of Bangladesh

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 →

Graft Failure after Haematopoietic Stem Cell Transplant

Haematology Society of Bangladesh

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 →

Establishing A Haematopoietic Stem Cell Transplantation Unit with Limited Resources

Haematology Society of Bangladesh Posted on 11/11/2019 by Editorial Staff06/07/2020

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 →

Diagnosing PNH with FLAER and Multiparameter Flow Cytometry: Our Experiences in Apollo Hospitals Dhaka

Haematology Society of Bangladesh

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 →

A Case of Diamond-Blackfan Anaemia with Ribosomal Protein S19 Mutation

Haematology Society of Bangladesh

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 →

Post navigation

<< 1 2 … 5 6 7 8 9 10 11 … 16 17 >>
Login/Register
Submit Your Article
2/1, Humayun Road, Mohammadpur, Dhaka 1207
&
Department of Haematology, National Institute of Cancer Research & Hospital, Mohakhali, Dhaka 1212

President: abedin43481@yahoo.com
International Affairs: ia@hematologybd.org
Office: office@hematologybd.org
Journal: journal@hematologybd.org

0 3 0 3 7 9
Users Today : 6
Total Users : 30379
Total views : 53041
©2023 - Haematology Society of Bangladesh Privacy Policy
↑
 

Loading Comments...