Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ahmed K. Yas"'
Autor:
Ahmed K. Yas, Ammar Al Qassab
Publikováno v:
Iraqi Journal of Information & Communication Technology, Vol 6, Iss 1 (2024)
The early detection of pipeline breaches in the pipeline monitoring system is a crucial concern for oil management firms. Diverse technologies have been created to identify pipeline leaks. However, they need development as the current systems take a
Externí odkaz:
https://doaj.org/article/ab0cf1603a6c48888e45a1e20e4727fa
Autor:
Ahmed K. Yas, Ammar Al Qassab
Publikováno v:
Iraqi Journal of Information and Communication Technology. 6:9-27
The early detection of pipeline breaches in the pipeline monitoring system is a crucial concern for oil management firms. Diverse technologies have been created to identify pipeline leaks. However, they need development as the current systems take a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0042b3599f0d39e07c46dc9d01506a68
https://doi.org/10.31987/ijict.6.1.209
https://doi.org/10.31987/ijict.6.1.209
Autor:
Mohammad S. Afana, Mohammad Abu-Tineh, Awni Alshurafa, Ahmed K. Yasin, Khalid Ahmed, Mohammed Abdulgayoom, Mohamed A. Yassin
Publikováno v:
Hematology, Vol 28, Iss 1 (2023)
ABSTRACTSickle cell disease (SCD) is one of the most common hematological diseases, which results in variable complications. The treatment of SCD is evolving but limited options are available for now. Acute chest syndrome (ACS) is one of the serious
Externí odkaz:
https://doaj.org/article/04148f6046f54c1aa1b3c9dfccac19ad
Autor:
Najmaddin Khoshnaw, Ahmed K. Yassin, Sana J. Dlawar, Alaa F. Alwan, Parween Kh. Ismael, Hameed S.M. Saeed, Layth Mula-Hussain
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 4, Pp 512-514 (2021)
Externí odkaz:
https://doaj.org/article/ac9f7658776e4b25a1368fa4e4a28cb4
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-6 (2020)
Abstract Background HbH disease results from dysfunction of three, less commonly two, α-globin genes through various combinations of deletion and non-deletion mutations. Characterization of the mutations and the underlying genotypes is fundamental f
Externí odkaz:
https://doaj.org/article/e5fa24afa56043fa955142e754cff9cc
Publikováno v:
Clinical Case Reports, Vol 7, Iss 11, Pp 2022-2026 (2019)
Abstract Myeloid sarcoma (MS) is a rare myeloid malignancy. It can arise before, concurrent with, or following different malignant hematological diseases, most commonly acute myeloid leukemia (AML), myelodysplastic syndrome, or myeloproliferative neo
Externí odkaz:
https://doaj.org/article/cf0d8842ef4c472aab5465db6ccf7865
Autor:
Lika'a Fasih Y. Al-Kzayer, Ahmed K. Yassin, Khalid Hama Salih, Tomonari Shigemura, Kenji Sano, Ruwaid Behnam Y. Al-Simaani, Miyuki Tanaka, Yozo Nakazawa, Yusuke Okuno
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Mendelian susceptibility to mycobacterial diseases (MSMD) is a rare condition of primary immunodeficiency disorder. Interleukin-12 receptor β1 (IL12RB1) deficiency, is the most common genetic etiology of MSMD, which is characterized by the selective
Externí odkaz:
https://doaj.org/article/1b7237ceff6d4582b8d8b62eda0cd576
Autor:
Ahmed K. Yassin
Publikováno v:
مجلة كلية الطب, Vol 55, Iss 2 (2013)
Background: Multiple myeloma is characterized by clonal expansion and accumulation of abnormal plasma cells in the bone marrow compartment. This study was conducted to determine the frequency and hematological presentation of multiple myeloma in Nana
Externí odkaz:
https://doaj.org/article/b068c05c77c740c2836233055082483b