Search Results - "Kabir, Amin Lutful"

  • Showing 1 - 13 results of 13
Refine Results
  1. 1

    Evaluation, Exploration and Management Strategies of a First Reported Rarest Case of Para-Bombay Blood Phenotype with E-Beta Thalassaemia from Bangladesh by Dipta, Tashmim Farhana, Kabir, Amin Lutful, Quader, Mohammed Abdul, Parvin, Farida, Khatun, Ayesha

    “…Human H/h genetic polymorphism in ABO blood group system is rare and evidenced with Bombay and Para-Bombay blood group. This patient a 27-year-old-young man…”
    Get full text
    Journal Article
  2. 2
  3. 3

    Frequency of consanguineous marriage among the thalassaemia major patients in Bangabandhu Sheikh Mujib Medical University by Mahzabin, Nishat, Islam, Ismat Ara, Dey, Mily, Jahan, Nusrat, Hasan Sajib, Md Kamrul, Shah, Md Salahuddin, Chowdhury, Romana, Aziz, Md Abdul, Kabir, Amin Lutful

    “…Thalassaemia is a commonly occurring hereditary disorder. There is a high prevalence of thalassaemia disease in South-East Asia as well as Bangladesh. It is an…”
    Get full text
    Journal Article
  4. 4

    Co-existence of Iron Deficiency in Beta Thalassaemia Trait by Mohammad, Nur, Chowdhury, MA Jalil, Alam, Md Rafiqul, Kabir, Amin Lutful, Rahaman, Mohammad Ferdous Ur, Chakrabarty, Baren

    Published in Journal of medicine (2018)
    “…Background: Beta-Thalassaemia Trait (β-TT) is common in this subcontinent as well as Bangladesh. 3% of our total population is documented to have β-TT. Iron…”
    Get full text
    Journal Article
  5. 5

    Arthritis as a presentation of acute leukemia by Aziz, Md. Abdul, Sarkar, Surozit Kumar, Rahman, Farzana, Islam, Shafiqul, Kabir, Amin Lutful, Begum, Masuda

    “…A 14 year old boy presented with 3 months history of low back pain as well as pain and swelling of both knee joints. The pain was inflammatory in nature. He…”
    Get full text
    Journal Article
  6. 6

    A Screening Test for Iron Deficiency Anaemia and Thalassaemia Traits by Kabir, Amin Lutful, Dipta, Tashmim Farhana, Khatun, Hajera, Rahman, Mohammad Hafizur, Haq, Mahfuz, Uddin, Mohammad Kazim, Begum, Masuda

    “…Both iron deficiency and thalassaemia trait can present with hypochromic microcytic morphology. Naked eye single tube red cell osmotic fragility (NESTROF) is…”
    Get full text
    Journal Article
  7. 7

    Haemoglobin E/Beta Thalassaemia- A Study in BSMMU by Aziz, Md Abdul, Begum, Masuda, Islam, Md Sirajul, Islam, Naima, Rahman, Md Jalilur, Kabir, Amin Lutful

    “…Background: Thalassaemias and haemoglobinopathies have been found sporadically in every ethnic group and geographic region, they occur with particularly high…”
    Get full text
    Journal Article
  8. 8

    Disseminated Histoplasmosis in Immunocompetent Patients Presented with Fever of Unknown Origin (FUO) by Islam, Md Sohidul, Habib, Md Rehan, Asha, Elmay Taswafe, Sharmin, Mahbuba, Ashraf, Mehnaj, Mahmud, Abdullah Al, Kabir, Amin Lutful, Alam, Md Rafiqul, Chowdhury, Fazle Rabbi

    Published in Journal of medicine (22-03-2023)
    “…Histoplasmosis is underreported although in Southeast Asia including Bangladesh is thought to be endemic considering the favorable geo-climatic conditions for…”
    Get full text
    Journal Article
  9. 9

    Frequency of consanguineous marriage among the thalassaemia major patients in Bangabandhu Sheikh Mujib Medical University by Nishat Mahzabin, Ismat Ara Islam, Mily Dey, Nusrat Jahan, Md Kamrul Hasan Sajib, Md Salahuddin Shah, Romana Chowdhury, Md Abdul Aziz, Amin Lutful Kabir

    “…Thalassaemia is a commonly occurring hereditary disorder. There is a high prevalence of thalassaemia disease in South-East Asia as well as Bangladesh. It is an…”
    Get full text
    Journal Article
  10. 10
  11. 11
  12. 12
  13. 13

    A Multicentre Based Observation of a Screening tool to Differentiate Microcytosis and Hypochromia by Dipta, Tashmim Farhana, Kabir, Amin Lutful, Rahman, Md Hafizur, Sultana, Gazi Sharmin, Hossain, Ahmed Zahid, Fatema, Nafisa, Ferdousi, Shamima

    Published in Anwer Khan Modern Medical College journal (16-02-2017)
    “…Back ground: Iron deficiency anemia (IDA) and beta-thalassaemia trait (B-TT) are the most common causes of hypochromic microcytic anemia. Many indices have…”
    Get full text
    Journal Article