Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nishat Mahzabin"'
Autor:
Nishat Mahzabin, Md Raiq Raihan Chowdhury, Md Akhlak Ul Islam, Ismat Ara Islam, Mily Dey, Md Salahuddin Shah, Md Abdul Aziz
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 15, Iss 2 (2023)
The COVID-19 pandemic has had a consequential impact on the global health system. Multisystem involvement is common in COVID-19. Many COVID-19 patients also showed changes in haematological parameters. This cross-sectional study included patients who
Externí odkaz:
https://doaj.org/article/50cf14f3e0924a7395fd434142a871eb
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. Raiq Raihan Chowdhury, Ishwor Man Singh, Nasrin Akhter, Samim Reza, Md. Maruf Reza Kabir, Kazi Fazlur Rahman, Nishat Mahzabin, Md. Salahuddin Shah, Md. Abdul Aziz
Publikováno v:
Haematology Journal of Bangladesh. 7:3-9
Introduction: Chronic Myeloid Leukaemia (CML) is a myeloproliferative neoplasm characterised by uncontrolled proliferation of white blood cells and its precursors. At diagnosis, various risk scoring systems have been formulated for risk stratificatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40aa1344e98072a1e5d617ca8f331aec
https://doi.org/10.37545/haematoljbd202396
https://doi.org/10.37545/haematoljbd202396
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
Publikováno v:
Journal of Computational Electronics. 20:116-125
This study investigates the differences in electron transport properties between metallic, semiconducting and topological insulator nanoribbons (NRs). Using non-equilibrium Green’s function (NEGF) formalism, we have considered transport of edge sta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::edb39021cdab34a07e7db73726337559
https://doi.org/10.1007/s10825-020-01608-0
https://doi.org/10.1007/s10825-020-01608-0
Autor:
Kazi Mohammad Kamrul Islam, Israt Jahan, Md Adnan Hasan Masud, Md. Golzar Hossain, Nishat Mahzabin, Md. Arif-Ur- Rahman, Munim Ahmed, Mujahida Rahman, Md. Salahuddin Shah, Md. Abdul Aziz, Masuda Begum, A B M Yunus
Publikováno v:
Haematology Journal of Bangladesh. 6
Background: Aberrant expression (AE) of Acute Leukaemia (AL) is essential to confirm the diagnosis of AL patients whether it is biphenotypic/mix phenotypic AL or it is AL with AE. Objectives: This study is conducted to observe the diversity of aberra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0742faafb03ac7a921d7ed5b7a3eab01
https://doi.org/10.37545/haematoljbd202283
https://doi.org/10.37545/haematoljbd202283
Autor:
Ismat Ara Islam, Md. Akhlak-Ul Islam, Mily Dey, Md. Abdullah Saeed Khan, Amin Lutful Kabir, Mohammad Jahid Hasan, Md. Abdul Aziz, Md. Kamrul Hasan Sajib, Nishat Mahzabin, Nusrat Jahan, Md. Raiq Raihan Chowdhury
Background: Hemoglobin E/β-thalassemia is a common inherited hemoglobin disorder among South Asian countries. The phenotypically diverse presentation of the disease is often attributed to coinheritance of β-globin (HBB) gene mutations. The current
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a355d4c28315d476760017a7bb46f22
https://doi.org/10.21203/rs.3.rs-927268/v1
https://doi.org/10.21203/rs.3.rs-927268/v1
Autor:
Khaza Amirul Islam, Nishat Mahzabin, Md. Salahuddin Shah, Md. Shafiul Azam, Md. Abdul Aziz, Md. Rafiquzzaman Khan
Publikováno v:
Haematology Journal of Bangladesh. 4:16-18
The aim of the study was to determine the frequency of hypothyroidism in transfusion dependent thalassaemia patients. A total of 64 transfusion dependent thalassaemia (TDT) patients were included in this cross-sectional study from April, 2018 to Sept
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f846c65178b83cf66c7b7f9a263e758
https://doi.org/10.37545/haematoljbd202049
https://doi.org/10.37545/haematoljbd202049
In this paper, we have investigated the transport of topological edge states in 2D Zigzag edge Tungsten Ditelluride Nanoribbon (ZTDNR).We have found that zigzag edge nanoribbon (NR) of Tungsten Ditelluride develops topological edge states in the pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad0acbb938953d75e406f69916fac59f
https://doi.org/10.21203/rs.3.rs-166455/v1
https://doi.org/10.21203/rs.3.rs-166455/v1
Publikováno v:
2020 11th International Conference on Electrical and Computer Engineering (ICECE).
The quantum transport properties of electrons in 2D hexagonal lattice Molybdenum di-selenide (MoSe 2 ) armchair and zigzag nanoribbons are investigated using Non-Equilibrium Green’s function (NEGF) formalism and 11- band Tight-Binding model. The ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef0c9261997c93eff33681338dd818cc
https://doi.org/10.1109/icece51571.2020.9393084
https://doi.org/10.1109/icece51571.2020.9393084