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Acta Bio-Medica : Atenei Parmensis|May 12, 2022
Cardio-protective effect of regular transfusion in children with non-transfusion dependent thalassemia (NTDT): A cohort studyKhalfan Al Senaidi, Surekha Maveda, Niranjan Joshi, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|October 24, 2018
Hemoglobin F as a predictor of health-related quality of life in children with sickle cell anemiaMohamed-Rachid Boulassel, Amira Al-Badi, Mohamed Elshinawy, et al.
Journal of Pediatric Hematology/Oncology|December 20, 2012
Transcranial Doppler ultrasonography in sickle cell disease: a study in Omani patientsArunodaya R Gujjar, Mathew Zacharia, Salam Al-Kindi, et al.
Transfusion|March 6, 2020
Preoperative transfusion versus no transfusion policy in sickle cell disease patients: a randomized trialMohamed Elshinawy, Nada Al Marhoobi, Rashid Al Abri, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 2, 2025
Health-Related Quality of Life in Egyptian Children With Haemophilia A and Chronic Arthropathy With the Era of Emicizumab Therapy: A Single-Centre Cohort StudyGehan Lotfy Abdel Hakeem Khalifa, Rawhya Rabei Abdel Tawab, Mohamed Ahmed Bahaa, et al.
Oman Medical Journal|December 6, 2021
Cognitive Function in Adults with Beta-Thalassemia Major in Oman: A Pilot StudyShahina Daar, Muna Al Saadoon, Yasser Wali, et al.
Oman Medical Journal|March 14, 2022
Incorporation of Evidence-based Guidelines on Bleeding Risk Assessment Prior to Surgery into Practice: Real-time ExperienceNada Al-Marhoobi, Manar Maktoom, Mohamed Elshinawy, et al.
American Journal of Ophthalmology|July 30, 2008
Orbital infarction in sickle cell diseaseAnuradha Ganesh, Sana Al-Zuhaibi, Anil Pathare, et al.
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