Search Results - "Albagshi, Muneer"

Bilateral chilaiditi syndrome in a child with sickle cell trait by Muneer H AlBagshi, Fatimah A Alaithan

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Prevalence of Glucose-6-Phosphate Dehydrogenase Deficiency Among Children in Eastern Saudi Arabia by Albagshi, Muneer H, Alomran, Suad, Sloma, Somaya, Albagshi, Murtadha, Alsuweel, Abdullah, AlKhalaf, Helal

“…Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common red blood cell enzyme deficiency worldwide. The disease is widely distributed…”
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Congenital thrombotic thrombocytopenic purpura simulating alloimmune thrombocytopenia by Albagshi, Muneer, Al Omran, Abbas, Elhakeem, Heba

“…Congenital thrombotic thrombocytopenic purpura (cTTP) is a thrombotic microangiopathic caused by severely reduced activity of the von Willebrand…”
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Sickle cell disease: High risk or no risk for coronavirus disease 2019 infection by Muneer Hassan Albagshi, Mahmoud H Albagshi

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Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area by Qari, Mohamad H, Wali, Yasser, Albagshi, Muneer H, Alshahrani, Mohammad, Alzahrani, Azzah, Alhijji, Ibrahim A, Almomen, Abdulkareem, Aljefri, Abdullah, Al Saeed, Hussain H, Abdullah, Shaker, Al Rustumani, Ahmad, Mahour, Khoutir, Mousa, Shaker A

“…Thalassemia syndrome has diverse clinical presentations and a global spread that has far exceeded the classical Mediterranean basin where the mutations arose…”
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Blood Demand and Challenges for Patients With Beta-Thalassemia Major in Eastern Saudi Arabia by Albagshi, Muneer H, Saad, Mona, Aljassem, Abdulmohsin M, Bushehab, Abdulaziz A, Ahmed, Noura H, Alabbad, Mahmoud M, Omer, Nawal, Alhamad, Osama A, Sultan, Tarig A, Bahgat, Samy

“…Background β-thalassemia major is a hereditary disorder of hemoglobin (Hb) that results in defective Hb synthesis, leading to severe chronic anemia. The…”
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Management of Glanzmann's Thrombasthenia – Guidelines based on an expert panel consensus from gulf cooperation council countries by Ahmad Tarawah, Tarek Owaidah, Naima Al-Mulla, Muhammad Faisal Khanani, Jehan Elhazmi, Muneer Albagshi, Yaser Wali, Shikah AlMohareb, Abdulkareem Almomen

“…Glanzmann thrombasthenia is a rare disorder, due to quantitative and/or qualitative abnormalities of the platelet integrin αIIbβ3 and/or αIIbβ3. Although it is…”
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Hereditary pyropoikilocytosis by Muneer Hassan Albagshi

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Sickle Cell Disease (SCD) Burden on Patients Treated With Hydroxyurea (HU): Results from the Real-World Assessment Survey for SCD in Saudi (ROARS) by Ezzat, Hatoon M., Al Zayed, Abdullah Hasan, Al Saeed, Hussain H., Al Darwish, Mohamed, Albagshi, Muneer, Malhan, Hafiz, Tarawah, Ahmad, Al Manea, Aljawhara, Alhazmi, Iman, Qari, Mohamed, Alzahrani, Azzah, Alzahrani, Mohsen, Soliman, Wesam, Askar, Farid, Yassin, Al Shaimaa, Jastaniah, Wasil

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Evidence Gaps in the Management of Patients with Sickle Cell Disease (SCD) by Non-specialist Healthcare Professionals (HCPs): Results from the Real-World Assessment Survey for SCD in Saudi (ROARS) by Jastaniah, Wasil, Al Zayed, Abdullah Hasan, Al Saeed, Hussain H., Al Darwish, Mohamed, Albagshi, Muneer, Malhan, Hafiz, Tarawah, Ahmad, Al Manea, Aljawhara, Alhazmi, Iman, Qari, Mohamed, Alzahrani, Azzah, Alzahrani, Mohsen, Soliman, Wesam, Askar, Farid, Almustafa, Sukina, Ezzat, Hatoon M.

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Congenital sideroblastic anemia of a Saudi child by ALBagshi, Muneer H, Saloma, Somaya H, Albagshi, Hassan M

“…Sideroblastic anemia is a heterogeneous group of disorders characterized by the presence of ring sideroblasts in the bone marrow, and has congenital and…”
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Infantile cortical hyperostosis - a report of Saudi family by ALBagshi, Muneer H, ALZoayed, Heji I

“…A 2-weeks-old Saudi neonate was apparently well till the 10th day of life when a swelling of the right groin was noted accompanied by irritability and fever,…”
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Congenital sideroblastic anemia of a Saudi child by ALBagshi, Muneer H, Saloma, Somaya H, Albagshi, Hassan M

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Infantile cortical hyperostosis - a report of Saudi family by ALBagshi, Muneer H, ALZoayed, Heji I

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