Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hussain H Al Saeed"'
Autor:
Ayman Alhejazi, Abdulkareem AlMomen, Ahmad M Tarawah, Ahmed M AlSuliman, Hussain H Al Saeed, Mahasen Saleh, Marwan ElBagoury, Ohoud F Kashari, Omar M Hussein
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 3, Pp 93-101 (2020)
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://doaj.org/article/30381f2b043045978efab62368f0d08e
Autor:
Mona M Alfaraj, Hussain H Al Saeed
Publikováno v:
Journal of Applied Hematology, Vol 11, Iss 1, Pp 1-6 (2020)
Pure red cell aplasia (PRCA) is a type of normocytic or sometimes macrocytic anemia characterized by reticulocytopenia. The cause of hypo erythropoiesis is varied. It could be of a congenital or an acquired type. A congenital PRCA is different than a
Externí odkaz:
https://doaj.org/article/de457e5351d84e8eb4f9eb55bba7f010
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:
Mahasen Saleh, Saud Balelah, Marwan ElBagoury, Fahad Alabbas, Hussain H Al Saeed, Mohamad H. Qari, Iman Alhazmi, Sherif Roushdy, Ohoud F. Kashari, Tarek Owaidah, Ghaleb Elyamany
Publikováno v:
Journal of Applied Hematology, Vol 12, Iss 3, Pp 123-133 (2021)
Gaucher disease (GD) is a lysosomal storage disorder that occurs due to an inherited inborn error of metabolism. GD manifested due to the deficient activity of the glucocerebrosidase enzyme that results in the accumulation of the harmful glucocerebro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac36bb982eedbbe5dc443becdf4c3f22
http://www.jahjournal.org/article.asp?issn=1658-5127
http://www.jahjournal.org/article.asp?issn=1658-5127
Autor:
Wasil Jastaniah, Abdullah Hasan Al Zayed, Hussain H. Al Saeed, Mohamed Al Darwish, Muneer Albagshi, Hafiz Malhan, Ahmad Tarawah, Aljawhara Al Manea, Iman Alhazmi, Mohamed Qari, Azzah Alzahrani, Mohsen Alzahrani, Wesam Soliman, Farid Askar, Sukina Almustafa, Hatoon M. Ezzat
Publikováno v:
Blood. 140:5133-5134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2af5919ce36f03900d1a26924c3f6361
https://doi.org/10.1182/blood-2022-166880
https://doi.org/10.1182/blood-2022-166880
Autor:
Hatoon M. Ezzat, Abdullah Hasan Al Zayed, Hussain H. Al Saeed, Mohamed Al Darwish, Muneer Albagshi, Hafiz Malhan, Ahmad Tarawah, Aljawhara Al Manea, Iman Alhazmi, Mohamed Qari, Azzah Alzahrani, Mohsen Alzahrani, Wesam Soliman, Farid Askar, Al Shaimaa Yassin, Wasil Jastaniah
Publikováno v:
Blood. 140:10879-10880
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8532656caf297a62bf792d7cd5c4e18
https://doi.org/10.1182/blood-2022-166723
https://doi.org/10.1182/blood-2022-166723
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:
Ayman Hejazi, Marwan ElBagoury, Ghaleb El Yamany, Abdulelah Ismail Qadi, Hussain H Al Saeed, Fahad Alabbas, Ohoud F. Kashari
Publikováno v:
Blood. 136:32-33
Rationale: Gaucher disease (GD) is the most common amongst the lysosomal storage disorders. Prevalence of GD in Saudi Arabia is not available in published literature and it is expected to be high and remains undiagnosed. In 2004, a Saudi study report
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::527e38f339e094b5d1b77b8a9dd7c3b0
https://doi.org/10.1182/blood-2020-140563
https://doi.org/10.1182/blood-2020-140563
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
Publikováno v:
Saudi medical journal. 25(10)
Thalassemia major is a hereditary disorder of hemoglobin synthesis resulting in severe anemia. Treatment consists of multiple blood transfusions, a complication of which is iron overload. Excessive iron is then deposited in almost all tissues but pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::71e864fbd02a7b996b21f89c75ed5fd4
https://pubmed.ncbi.nlm.nih.gov/15494799
https://pubmed.ncbi.nlm.nih.gov/15494799