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Diagnostics (Basel, Switzerland)|March 29, 2023
Applications of Artificial Intelligence in ThrombocytopeniaAmgad M Elshoeibi, Khaled Ferih, Ahmed Adel Elsabagh, et al.
European Journal of Haematology|March 16, 2013
Optimizing Hydroxyurea use in children with sickle cell disease: low dose regimen is effectiveSharef Waadallah Sharef, Maya Al-Hajri, Ismail Beshlawi, et al.
Frontiers in Oncology|November 24, 2025
Consensus on managing delayed methotrexate elimination in high-dose therapy: insights from the Middle EastMubarak Al Manasour, Ahmad Absi, Ahmad Alhuraiji, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 22, 2016
Home treatment of haemarthrosis with recombinant activated factor VII in patients with haemophilia A or B and inhibitors: experience from developing countriesMeriem Bensadok, Abdulkareem Almomen, Azzam Alzoebie, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|April 11, 2017
Regulatory B Cells Are Functionally Impaired in Patients Having Hemophilia A With InhibitorsMohamed-Rachid Boulassel, Maryam Al-Ghonimi, Badriya Al-Balushi, et al.
Orphanet Journal of Rare Diseases|September 19, 2013
Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf areaMohamad H Qari, Yasser Wali, Muneer H Albagshi, et al.
Journal of Nutritional Science|July 15, 2022
Middle East consensus recommendations on the use of young child formula (YCF) in toddlersMohammed Al-Biltagi, Wafaa Faysal, Fatoumah Alabdulrazzaq, et al.
Mediterranean Journal of Hematology and Infectious Diseases|March 16, 2017
β-Thalassemia Distribution in the Old World: an Ancient Disease Seen from a Historical StandpointVincenzo De Sanctis, Christos Kattamis, Duran Canatan, et al.
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