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Rajaa Marouf

Showing results (1-10 of 16) with videos related to

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Hemoglobin|October 11, 2011
Blood transfusion in sickle cell diseaseRajaa Marouf
Acta Haematologica|December 4, 2009
Pattern of bone mineral density in sickle cell disease patients with the high-Hb F phenotypeRenu Gupta, Rajaa Marouf, Adekunle Adekile
Acta 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 Marouf
Journal 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 Marouf
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 8, 2007
Body iron stores in relation to the metabolic syndrome, glycemic control and complications in female patients with type 2 diabetesOlusegun A Mojiminiyi, Rajaa Marouf, Nabila A Abdella
Hemoglobin|May 31, 2019
The Sub-Phenotypes of Sickle Cell Disease in KuwaitAdekunle D Adekile, Sondus Al-Sherida, Rajaa Marouf, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|January 15, 2024
Determination of vWF, ADAMTS-13 and Thrombospondin-1 in Venous Thromboembolism and Relating Them to the Presence of Factor V Leiden MutationAnwar Al-Awadhi, Rajaa Marouf, Mehrez M Jadaon, et al.
Archives of Pathology & Laboratory Medicine|May 3, 2014
Circulating cell-free DNA in sickle cell disease: is it a potentially useful biomarker?Salah Al-Humood, Rajaa Zueriq, Lama Al-Faris, et al.
Annals of Hematology|April 2, 2021
Neutrophil gelatinase-associated lipocalin as a biomarker of nephropathy in sickle cell diseaseRajaa Marouf, Adekunle D Adekile, Hadeel El-Muzaini, et al.
Acta Haematologica|November 27, 2009
Hypercoagulable state and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with beta-thalassemia major in KuwaitNada Y Mustafa, Rajaa Marouf, Salah Al-Humood, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Hemoglobin|October 11, 2011
Blood transfusion in sickle cell diseaseRajaa Marouf
Acta Haematologica|December 4, 2009
Pattern of bone mineral density in sickle cell disease patients with the high-Hb F phenotypeRenu Gupta, Rajaa Marouf, Adekunle Adekile
Acta 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 Marouf
Journal 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 Marouf
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|December 8, 2007
Body iron stores in relation to the metabolic syndrome, glycemic control and complications in female patients with type 2 diabetesOlusegun A Mojiminiyi, Rajaa Marouf, Nabila A Abdella
Hemoglobin|May 31, 2019
The Sub-Phenotypes of Sickle Cell Disease in KuwaitAdekunle D Adekile, Sondus Al-Sherida, Rajaa Marouf, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|January 15, 2024
Determination of vWF, ADAMTS-13 and Thrombospondin-1 in Venous Thromboembolism and Relating Them to the Presence of Factor V Leiden MutationAnwar Al-Awadhi, Rajaa Marouf, Mehrez M Jadaon, et al.
Archives of Pathology & Laboratory Medicine|May 3, 2014
Circulating cell-free DNA in sickle cell disease: is it a potentially useful biomarker?Salah Al-Humood, Rajaa Zueriq, Lama Al-Faris, et al.
Annals of Hematology|April 2, 2021
Neutrophil gelatinase-associated lipocalin as a biomarker of nephropathy in sickle cell diseaseRajaa Marouf, Adekunle D Adekile, Hadeel El-Muzaini, et al.
Acta Haematologica|November 27, 2009
Hypercoagulable state and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with beta-thalassemia major in KuwaitNada Y Mustafa, Rajaa Marouf, Salah Al-Humood, et al.
Pageof 2