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Journal of Infection and Public Health|February 21, 2012
Complications of PORT-A-CATH® in patients with sickle cell diseaseSalam Alkindi, Samaa Matwani, Alghalia Al-Maawali, et al.
Sultan Qaboos University Medical Journal|October 25, 2017
Impact of Educational Activities in Reducing Pre-Analytical Laboratory Errors: A quality initiativeHamed Al-Ghaithi, Anil Pathare, Sahimah Al-Mamari, et al.
Scientific Reports|February 14, 2020
Predictors of impending acute chest syndrome in patients with sickle cell anaemiaSalam Alkindi, Ikhlas Al-Busaidi, Bushra Al-Salami, et al.
Archives of Medical Research|September 12, 2007
Trisomy 21 as a sole acquired abnormality in an adult Omani patient with CD7- and CD9-positive acute myeloid leukemiaAchandira M Udayakumar, Anil V Pathare, S Muralitharan, et al.
Hemoglobin|March 23, 2011
Hb Sheffield [β58(E2)Pro→His] in Oman: potential pitfall in genetic counselingShoaib Al Zadjali, Shahina Daar, Salam AlKindi, et al.
Contemporary Clinical Trials|September 12, 2021
A reanalysis of pain crises data from the pivotal l-glutamine in sickle cell disease trialAhmar U Zaidi, Jeremie Estepp, Nirmish Shah, et al.
Mediterranean Journal of Hematology and Infectious Diseases|March 16, 2017
Alloimmunization in Patients with Sickle Cell Disease and Thalassemia: Experience of a Single Centre in OmanSalam Alkindi, Saba AlMahrooqi, Sumaiya AlHinai, et al.
Blood Reviews|October 22, 2023
Management of transfusion-dependent β-thalassemia (TDT): Expert insights and practical overview from the Middle EastAmal El-Beshlawy, Hany Dewedar, Salwa Hindawi, et al.
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