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Page 1
Haemostatic Parameters in Patients with Behçet's Disease.
Alkaabi JK, Gravell D, Al-Haddabi H, Pathare A. Alkaabi JK, et al. Among authors: al haddabi h. Sultan Qaboos Univ Med J. 2014 May;14(2):e190-6. Epub 2014 Apr 7. Sultan Qaboos Univ Med J. 2014. PMID: 24790741 Free PMC article.
Clinical and Laboratory Features of Hemoglobin La Desirade Variant in Association with Sickle Cell and Alpha Thalassemia Genes.
Alkindi S, Al Zadjali S, Al Rawahi M, Al Haddabi H, Daar S, ElSadek RA, Sherkawy BD, Pathare AV. Alkindi S, et al. Among authors: al haddabi h. Mediterr J Hematol Infect Dis. 2021 Jan 1;13(1):e2021010. doi: 10.4084/MJHID.2021.010. eCollection 2021. Mediterr J Hematol Infect Dis. 2021. PMID: 33489049 Free PMC article. No abstract available.
Hereditary thrombophilia in ethnic Omani patients.
Pathare A, Al Kindi S, Al Haddabi H, Dennison D, Bayoumi R, Muralitharan S. Pathare A, et al. Among authors: al haddabi h. Am J Hematol. 2006 Feb;81(2):101-6. doi: 10.1002/ajh.20525. Am J Hematol. 2006. PMID: 16432849 Free article.
Hb A2' (Hb B2) in the Omani population and diagnostic significance.
Daar S, Al Zadjali S, Gravell D, Al Haddabi H, Al Riyami M, Al Belushi A, Berbar T, Krishnamoorthy R. Daar S, et al. Among authors: al haddabi h. Hemoglobin. 2011;35(2):117-24. doi: 10.3109/03630269.2011.553557. Hemoglobin. 2011. PMID: 21417568