Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ahmed M Al-Suliman"'
Autor:
Hazzaa Al-Zahrani, Aamer Aleem, Fahad Al Mohareb, Said Yousuf Ahmed, Ahmed M Al-Suliman, Hussain H Al Saeed, Mubarak S Al-Ghamdi, Hani Al-Hashmi
Publikováno v:
Journal of Applied Hematology, Vol 10, Iss 3, Pp 77-83 (2019)
Immune thrombocytopenia (ITP) is a disorder characterized by an isolated thrombocytopenia in the absence of an identifiable cause. Management of ITP patients varies according to the clinical presentation, physicians' experience, availability of resou
Externí odkaz:
https://doaj.org/article/7f2e6ca56bd94e2ebf59b5f9b8632fd7
Autor:
Marwan ElBagoury, Ayman Alhejazi, Ahmad M Tarawah, Ohoud F. Kashari, Ahmed M. Al-Suliman, Omar M. Hussein, Abdulkareem Al-Momen, Mahasen Saleh, Hussain H Al Saeed
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 3, Pp 93-101 (2020)
BASE-Bielefeld Academic Search Engine
BASE-Bielefeld Academic Search Engine
INTRODUCTION: Gaucher disease is a challenging disease because of the progressive nature and multiple systems that are involved. Gaucher disease is underdiagnosed in Saudi Arabia. It is sometimes misdiagnosed with other hematological diseases. The pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::628a923a839640029c65381bdcd51e36
http://www.jahjournal.org/article.asp?issn=1658-5127
http://www.jahjournal.org/article.asp?issn=1658-5127
Autor:
Sana Al-Jarrash, J. Francis Borgio, Zaki A. Naserullah, Sayed AbdulAzeez, Ahmed M. Al-Suliman, Huda I. ElFakharay, Noor B. Almandil
Publikováno v:
Molecular Biology Reports. 47:603-606
In the Eastern province of Saudi Arabia, thalassemia is highly common. Data on the effect of alpha globin gene variation on the concentration of iron on transfusion dependent Saudis are scanty. A total of 166 transfusions dependent β-thalassemia wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cc7c19f77e0b5ee5390ff3076f8400a
https://doi.org/10.1007/s11033-019-05168-w
https://doi.org/10.1007/s11033-019-05168-w
Publikováno v:
Genetic Testing and Molecular Biomarkers. 22:561-567
Sickle cell disease (SCD) is a monogenic disease that has wide variety of phenotypes with both and environmental factors contributing to its severity.We performed whole-exome sequencing (WES) in 22 Saudi SCD patients to identify variants that could e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7859ef8ad20bd5d4f7737b50f12a443c
https://doi.org/10.1089/gtmb.2018.0058
https://doi.org/10.1089/gtmb.2018.0058
Autor:
Ahmed M. Al-Suliman, Reem Sayeb Al-Atrash, Eman R. Albukhari, Ziyad T. Al-Ghannam, Neriman Sadek Al-Ali, Zhara A. Al-Ali, Rana K. Fallatah, Chittibabu Vatte, Esra A. Aljaffer
Publikováno v:
Acta Haematologica. 140:55-59
Disease severity of sickle cell anemia is highly variable, and it is commonly accepted that fetal hemoglobin (HbF) levels play a major role as an ameliorating factor. Investigation of genetic variants have identified several genes to be the principal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d402157ad177dca1915546a3a5deaab4
https://doi.org/10.1159/000491688
https://doi.org/10.1159/000491688
Autor:
Sayed AbdulAzeez, Amein K. Al-Ali, J. Francis Borgio, Ahmed M. Al-Muslami, Ahmed M. Al-Suliman, Mohammed S. Al-Madan, Zaki A. Naserullah, Sana Al-Jarrash
Publikováno v:
Archives of Medical Science : AMS
Introduction Elevated HbA2 (hemoglobin A2) level is considered the most reliable hematological parameter for the detection of β-thalassemia carriers. However, some carriers are difficult to recognize because the level of HbA2 is not in the distincti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d08d1f53553cae59b0e1da3b05e7df7
http://europepmc.org/articles/PMC5778434
http://europepmc.org/articles/PMC5778434
Autor:
George J. Murphy, Hatem O. Qutub, P.K. Patra, Abdulrahman Alsultan, Hong-Yuan Luo, Shuai Wang, Zaki A. Naserullah, David H.K. Chui, Heather L. Edward, Heather Shappell, Vinod Vathipadiekal, Irene Simkin, Paola Sebastiani, Zhihua Jiang, Shengwen Huang, Fahad Al-Muhanna, Ahmed M. Al-Suliman, Gustavo Mostoslavsky, John J. Farrell, Lindsay A. Farrer, Abdullah M. Al-Rubaish, Martin H. Steinberg, Amein K. Al-Ali
Publikováno v:
American Journal of Hematology. 91:1118-1122
Fetal hemoglobin (HbF) levels are higher in the Arab-Indian (AI) β-globin gene haplotype of sickle cell anemia compared with African-origin haplotypes. To study genetic elements that effect HbF expression in the AI haplotype we completed whole genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eda24699e02c1b2bea09c03f4e14e066
https://doi.org/10.1002/ajh.24527
https://doi.org/10.1002/ajh.24527
Autor:
Zaki A. Naserullah, Jacqueline N. Milton, Ahmed M. Al-Suliman, Duyen A. Ngo, Abdullah M. Al-Rubaish, David H.K. Chui, Lindsay A. Farrer, Shuai Wang, Amein K. Al-Ali, Harold Bae, Paola Sebastiani, Heather L. Edward, Heather Shappell, Clinton T. Baldwin, Martin H. Steinberg, Vinod Vathipadiekal, Abdulrahman Alsultan, Fahad Al-Muhanna, P.K. Patra, John J. Farrell
Publikováno v:
Blood Cells, Molecules, and Diseases. 54:224-230
Background : Fetal hemoglobin (HbF) levels in sickle cell anemia patients vary. We genotyped polymorphisms in the erythroid-specific enhancer of BCL11A to see if they might account for the very high HbF associated with the Arab–Indian (AI) haplotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::baceebd04519dd420f69898220abdd5b
https://doi.org/10.1016/j.bcmd.2015.01.001
https://doi.org/10.1016/j.bcmd.2015.01.001
Autor:
Wala R Alanazi, Donna K. McClish, Anwar Ahmed, Jafar M. Albagshi, Ahmed M Al-Suliman, Mohieldin Elsayid, Hamdan Al-Jahdali, Rayan A Ahmed, Yosra Z. Ali, Majid Al Salamah
Publikováno v:
Journal of Blood Medicine
Anwar E Ahmed,1 Yosra Z Ali,2 Ahmad M Al-Suliman,3 Jafar M Albagshi,3 Majid Al Salamah,1 Mohieldin Elsayid,1 Wala R Alanazi,4 Rayan A Ahmed,5 Donna K McClish,6 Hamdan AL-Jahdali,1,2 1College of Public Health and Health Informatics, King Saud bin Abdu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e00d20d32dd1d0a916a4798fcf7c74ed
https://www.dovepress.com/the-prevalence-of-abnormal-leukocyte-count-and-its-predisposing-factor-peer-reviewed-article-JBM
https://www.dovepress.com/the-prevalence-of-abnormal-leukocyte-count-and-its-predisposing-factor-peer-reviewed-article-JBM
Autor:
Ohoud F. Kashari, Hussain H Al Saeed, Ahmed M. Al-Suliman, Omar M. Hussein, Mahsen AlSaleh, Abdulkareem Al-Momen, Marwan ElBagoury, Ayman Alhejazi, Ahmad M Tarawah
Publikováno v:
Blood. 134:4864-4864
Background and Objectives Management and treatment of Gaucher disease are quite challenging because of its progressive nature and multisystem involvement. Gaucher disease is misdiagnosed or underdiagnosed in Saudi Arabia due to the high practice of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e86c7030ff458229de3216442e3296ab
https://doi.org/10.1182/blood-2019-122822
https://doi.org/10.1182/blood-2019-122822