Citations (9)
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Tamanna Kabir, Saeed Anwar, Jarin Taslem Mourosi, Shanjida Akter & Mohammad Jakir Hosen. (2023) α- and β-Globin Gene Mutations in Individuals with Hemoglobinopathies in the Chattogram and Sylhet Regions of Bangladesh. Hemoglobin 47:1, pages 3-10.
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Mahmood A. Chowdhury, Razia Sultana & Dhananjoy Das. (2022) Thalassemia in Asia 2021 Overview of Thalassemia and Hemoglobinopathies in Bangladesh. Hemoglobin 46:1, pages 7-9.
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Md. Abdul Aziz, Waqar A. Khan, Bilquis Banu, Sudipta A. Das, Salma Sadiya & Sayeda Begum. (2020) Prenatal Diagnosis and Screening of Thalassemia Mutations in Bangladesh: Presence of Rare Mutations. Hemoglobin 44:6, pages 397-401.
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Kallol Kumar Bhattacharyya, Tridip Chatterjee & Ujjalendu Bikash Mondal. (2016) A comprehensive screening program for β-thalassemia and other hemoglobinopathies in the Hooghly District of West Bengal, India, dealing with 21 137 cases. Hemoglobin 40:6, pages 396-399.
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Articles from other publishers (5)
Nur E. Alam, Md Shariful Islam, Md Imam Ul Khabir, Umme Suriea, Md Muzahidul Islam, Ramisa Binti Mohiuddin, Sumaiya Akter, Nahid Mahamud, Md Nazmul Islam Bappy, Dipankar Sardar, Shahin Mahmud, Kamal Chowdhury & A. K. M. Mohiuddin. (2022) The scenario of knowledge, attitude and practice of the Bangladeshi population towards thalassemia prevention: A nationwide study. PLOS Global Public Health 2:10, pages e0001177.
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Salma Afrose. (2022) Editorial. Haematology Journal of Bangladesh 6:02.
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Md Tarikul Islam, Suprovath Kumar Sarkar, Nusrat Sultana, Mst. Noorjahan Begum, Golam Sarower Bhuyan, Shezote Talukder, A. K. M. Muraduzzaman, Md Alauddin, Mohammad Sazzadul Islam, Pritha Promita Biswas, Aparna Biswas, Syeda Kashfi Qadri, Tahmina Shirin, Bilquis Banu, Salma Sadya, Manzoor Hussain, Golam Sarwardi, Waqar Ahmed Khan, Mohammad Abdul Mannan, Hossain Uddin Shekhar, Emran Kabir Chowdhury, Abu Ashfaqur Sajib, Sharif Akhteruzzaman, Syed Saleheen Qadri, Firdausi Qadri & Kaiissar Mannoor. (2018) High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genetics 19:1.
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Suprovath Kumar Sarker, Md Tarikul Islam, Golam Sarower Bhuyan, Nusrat Sultana, Mst. Noorjahan Begum, Mohammad Al Mahmud-Un-Nabi, Md. Abdulla Al Noman Howladar, Tashmim Farhana Dipta, A.K.M. Muraduzzaman, Syeda Kashfi Qadri, Tahmina Shirin, Salma Sadiya, Manzoor Hussain, Waqar Ahmed Khan, Sharif Akhteruzzaman, Syed Saleheen Qadri, Firdausi Qadri & Kaiissar Mannoor. (2018) Impaired acylcarnitine profile in transfusion-dependent beta-thalassemia major patients in Bangladesh. Journal of Advanced Research 12, pages 55-66.
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Mohammad Sorowar Hossain, Enayetur Raheem, Tanvira Afroze Sultana, Shameema Ferdous, Nusrat Nahar, Sazia Islam, Mohammad Arifuzzaman, Mohammad Abdur Razzaque, Rabiul Alam, Sonia Aziz, Hazera Khatun, Abdur Rahim & Manzur Morshed. (2017) Thalassemias in South Asia: clinical lessons learnt from Bangladesh. Orphanet Journal of Rare Diseases 12:1.
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