Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Amin Lutful Kabir"'
Autor:
Mohammad Aminul Islam, Amin Lutful Kabir, Zahed Khan, Mahbubur Rahman, Mohammad Abdul Aziz, Rumana Rashid, Col Huque Mahfuz, Col. Mohammed Mosleh Uddin, Afrose Salma, Shahed Chowdhury, Farida Arjuman, Mostafa Sumon, Tasbirul Islam, Jonathan Mo
Publikováno v:
HemaSphere, Vol 7, p e5593736 (2023)
Externí odkaz:
https://doaj.org/article/dd322025013a47419a3a78c731b417eb
Autor:
Nishat Mahzabin, Ismat Ara Islam, Mily Dey, Nusrat Jahan, Md Kamrul Hasan Sajib, Md Salahuddin Shah, Romana Chowdhury, Md Abdul Aziz, Amin Lutful Kabir
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 15, Iss 1 (2022)
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 autosomal recessive disorder, so consanguineous marriage is a very important factor for th
Externí odkaz:
https://doaj.org/article/3a215b536498438687a5900f22530270
Autor:
Md. Abdul Aziz, Surozit Kumar Sarkar, Farzana Rahman, Shafiqul Islam, Amin Lutful Kabir, Masuda Begum
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 9, Iss 4 (2016)
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 was thoroughly evaluated but no underlying cause was detected. However, the boy was treated w
Externí odkaz:
https://doaj.org/article/772945aa9ebb4fbc91eaf85d4a68790e
Autor:
Md Abdul Aziz, Masuda Begum, Md Sirajul Islam, Naima Islam, Md Jalilur Rahman, Amin Lutful Kabir
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 2, Iss 2 (2010)
Background: Thalassaemias and haemoglobinopathies have been found sporadically in every ethnic group and geographic region, they occur with particularly high frequency from the shores of the Mediterranean and Africa through the Middle East, the India
Externí odkaz:
https://doaj.org/article/444bfd212b914d5fb6469390f610955e
Disseminated Histoplasmosis in Immunocompetent Patients Presented with Fever of Unknown Origin (FUO)
Autor:
Md Sohidul Islam, Md Rehan Habib, Elmay Taswafe Asha, Mahbuba Sharmin, Mehnaj Ashraf, Abdullah Al Mahmud, Amin Lutful Kabir, Md Rafiqul Alam, Fazle Rabbi Chowdhury
Publikováno v:
Journal of Medicine. 24:59-64
Histoplasmosis is underreported although in Southeast Asia including Bangladesh is thought to be endemic considering the favorable geo-climatic conditions for the organism. Non-recognition of histoplasmosis is particularly attributed to possible misd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e607bbf054baa15daa6a81215add96cc
https://doi.org/10.3329/jom.v24i1.64906
https://doi.org/10.3329/jom.v24i1.64906
Autor:
Nasrin Akhter, Amin Lutful Kabir, M T Islam, Md. Abdul Aziz, A B M Yunus, Masuda Begum, Salahuddin Shah, Rafiquzzaman Khan, Farzana Rahman
Publikováno v:
Haematology Journal of Bangladesh. 7:10-17
Background: Haemophilia is a sex-linked bleeding disorder. Affected patients suffer spontaneous or post-traumatic bleeding into various sites of the body, mainly into joints, depending on the level of coagulation factor deficiency. Recurrent joint bl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5211dcc8b7b5b2de8f00f9cb072647e2
https://doi.org/10.37545/haematoljbd202397
https://doi.org/10.37545/haematoljbd202397
Autor:
Dr. Tanjina Afrin, Professor Dr. A B M Yunus, Professor Dr. Abdul Aziz, Professor Dr. Salahuddin Shah, Dr. Amin Lutful Kabir, Dr. Md. Adnan Hasan Masud, Dr. Mahbuba Sharmin, Dr. A.Q.M. Ashraful Haque
Publikováno v:
Scholars Journal of Applied Medical Sciences. 10:536-542
Background: Tumor lysis syndrome (TLS) is the combination of metabolic and electrolyte abnormalities (hyperuricemia, hyperkalaemia, hyperphosphatemia, and secondary hypocalcemia) which occurs in patients with cancer spontaneously and usually after th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19a6fe7f982ce46aaa83459fc1bf543e
https://doi.org/10.36347/sjams.2022.v10i04.017
https://doi.org/10.36347/sjams.2022.v10i04.017
Autor:
Dr. Tanjina Afrin, Dr. A B M Yunus, Dr. Abdul Aziz, Dr. Mahbuba Sharmin, Dr. Salahuddin Shah, Dr. Amin Lutful Kabir, Dr. Md. Adnan Hasan Masud, Dr. Shahidul Islam, Dr. Kazi Md Kamrul Islam
Publikováno v:
Saudi Journal of Medical and Pharmaceutical Sciences. 8:200-204
Background: ALL is a malignancy of B or T lymphoblasts which is characterized by unrestrained spread of abnormal, immature lymphocytes and their progenitors which results in the replacement of bone marrow and other lymphoid organs subsequently. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc1903564ed131d5dc94b9c8f5734545
https://doi.org/10.36348/sjmps.2022.v08i04.007
https://doi.org/10.36348/sjmps.2022.v08i04.007
Autor:
Amin Lutful Kabir, Nishat Mahzabin, Khaza Amirul Islam, Kazi Mohammad Kamrul Islam, Nusrat Jahan, Md. Arif-Ur Rahman, Md. Akhlak-Ul Islam
Publikováno v:
Haematology Journal of Bangladesh. 5:57-60
Background: Hb-E/Beta thalassaemia is a congenital haemoglobin disorder which is a compound heterozygous state consists of qualitative disorder like Hb E variant & quantitative Hb disorder caused by genetic mutation of Beta chain. Objective: The aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::921d1bc916bc3c4cea5fbe434c4d5441
https://doi.org/10.37545/haematoljbd202177
https://doi.org/10.37545/haematoljbd202177
Autor:
Mahbuba Sharmin, Md. Arif-Ur Rahman, Amin Lutful Kabir, Khaza Amirul Islam, Md. Shafiul Azam, Tahmina Akther, Saqi Md. Abdul Baqi
Publikováno v:
Haematology Journal of Bangladesh. 5:47-49
The aim of the study was to determine serum ferritin level in transfusion dependent thalassaemia patients. A total of 64 transfusion dependent thalassaemia (TDT) patients was included in this cross sectional study from April, 2018 to September, 2019
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c6374ad723e5ecf1105fee32359d8f8
https://doi.org/10.37545/haematoljbd202172
https://doi.org/10.37545/haematoljbd202172