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Hemoglobin|February 6, 2020
α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean RegionArwa Z Al-Riyami, Shahina Daar, Salam Al Kindi, et al.
European Journal of Haematology|March 18, 2011
Severity ranking of non-deletional alpha thalassemic alleles: insights from an Omani family studyYasser Wali, Shoaib Al Zadjali, Mohamed Elshinawy, et al.
Clinical Immunology (Orlando, Fla.)|November 15, 2019
Elevated levels of circulating invariant natural killer cell subsets are skewed toward Th2-like phenotype in children with sickle cell diseaseMohamed-Rachid Boulassel, Abeer Al-Zubaidi, Shoaib Al-Zadjali, et al.
Sultan Qaboos University Medical Journal|February 25, 2016
Single Breath-Hold Physiotherapy Technique: Effective tool for T2* magnetic resonance imaging in young patients with thalassaemia majorSurekha T Mevada, Najma Al-Mahruqi, Ismail El-Beshlawi, et al.
European Journal of Haematology|May 15, 2013
A stepwise α-thalassemia screening strategy in high-prevalence areasSalam S Alkindi, Shoaib Alzadjali, Shahina Daar, et al.
TH Open : Companion Journal to Thrombosis and Haemostasis|July 2, 2019
HAEMOcare: The First International Epidemiological Study Measuring Burden of Hemophilia in Developing CountriesNaresh Gupta, Abderrahmane Benbouzid, Meriem Belhani, et al.
European Journal of Haematology|July 5, 2012
Coexistence of sickle cell disease and severe congenital neutropenia: first impressions can be deceivingYasser Wali, Ismail Beshlawi, Naglaa Fawaz, et al.
Frontiers in Cardiovascular Medicine|January 1, 2024
Thrombopoietin-receptor agonists for adult patients with immune thrombocytopenia: a narrative review and an approach for managing patients fasting intermittentlyMohamed A Yassin, Mona Al-Rasheed, Murtadha Al-Khaboori, et al.
Journal of Pediatric Hematology/Oncology|August 27, 2019
Pulmonary Artery Pseudoaneurysm in a Child With β-Thalassemia MajorTabinda N Qureshi, Syed R Haider, Abdulhakim Al Rawas, et al.
British Journal of Haematology|August 20, 2008
Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosisAnnaCarin Horne, Kim Göransdotter Ramme, Eva Rudd, et al.
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