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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|July 4, 2019
First description of the molecular and clinical characterization of hereditary factor V deficiency in Saudi Arabia: report of four novel mutationsNouf S Al-Numair, Khushnooda Ramzan, Mahasen Saleh, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|August 1, 2023
Genotype Hemophilia Screening Program Identified 2 Novel Variants Including a Novel Variant (c.5816-2A > G) Causing a Pathogenic Variant of the Factor 8 GeneTarek Owaidah, Salwa Bakr, Nouf Al-Numair, et al.
Cureus|April 7, 2022
Thromboembolic Events Burden in Patients With Solid Tumors and Their Predisposing FactorsShouki Bazarbashi, Turkiah Alkhaldi, Mohamed Aseafan, et al.
Saudi Journal of Gastroenterology : Official Journal of the Saudi Gastroenterology Association|March 7, 2025
Emerging need for a hepato-hematology program for patients with sickle cell disease in Saudi ArabiaBandar Al-Judaibi, Hazzaa Alzahrani, Ali Alahmari, et al.
Journal of Family Medicine and Primary Care|January 8, 2019
Associated head injuries and survival rate of patients with maxillofacial fractures in road traffic accident: A prospective study in Saudi ArabiaOmar Mufi Aldwsari, Khalid Hadi Aldosari, Musab Khader Alzahrani, et al.
Frontiers in Oncology|May 24, 2023
The role of androgen therapy in acquired aplastic anemia and other bone marrow failure syndromesMomen Nassani, Riad El Fakih, Jakob Passweg, et al.
Blood Research|April 22, 2026
Prognostic significance of PNH clones in aplastic anemia treated with immunosuppression or allogeneic HSCT: a 20-year single-center experienceAlfadil Haroon, Hazzaa Alzahrani, Mostafa F Mohammed Saleh, et al.
Communications Medicine|August 15, 2025
Haplo-stem cell transplant post liver transplantation to cure sickle cell disease with related liver dysfunction: a case seriesAli D Alahmari, Saad Alghamdi, Reem Alasbali, et al.
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