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Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|August 17, 2005
Mutations associated with beta-thalassemia intermedia in KuwaitAdekunle Adekile, Mohammad Haider, Ferdane KutlarBMC Medical Genetics|August 25, 2020
Alpha thalassemia genotypes in KuwaitAdekunle Adekile, Jalaja Sukumaran, Diana Thomas, et al.Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|June 2, 2007
Hemoglobin F concentration as a function of age in Kuwaiti sickle cell disease patientsAdekunle Adekile, Mohammed Al-Kandari, Mohammad Haider, et al.Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|September 6, 2020
The Genetic and Clinical Significance of Fetal Hemoglobin Expression in Sickle Cell DiseaseAdekunle AdekileMedical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|August 8, 2008
Ten-year review of hospital admissions among children with sickle cell disease in KuwaitNajwa Ali Akar, Adekunle AdekileActa Haematologica|December 4, 2009
Pattern of bone mineral density in sickle cell disease patients with the high-Hb F phenotypeRenu Gupta, Rajaa Marouf, Adekunle AdekileActa Haematologica|September 28, 2020
Relationship of Thrombospondin 1 to von Willebrand Factor and ADAMTS-13 in Sickle Cell Disease Patients of Arab EthnicityAnwar Al-Awadhi, Adekunle Adekile, Rajaa MaroufJournal of Thrombosis and Thrombolysis|September 11, 2016
Evaluation of von Willebrand factor and ADAMTS-13 antigen and activity levels in sickle cell disease patients in KuwaitAnwar Al-Awadhi, Adekunle Adekile, Rajaa MaroufHemoglobin|January 8, 2015
A new Aγ-globin chain variant: Hb F-Sykesville MD [Aγ113(G15)Val → Ile; HBG1: c.340G>A] detected in a Caucasian babyNiren Patel, Jason Fixler, Yoram Unguru, et al.Pageof 8