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 Combining Serology and Molecular Typing of Weak D Typing Strategy in Egypt. |
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Multidrug and Toxin ExtrusionProtein (MATE1) Gene Polymor-phism and Therapeutic Effects of Metformin in Type 2 Diabetes |
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Cystathionine Beta Synthase (CBS) Gene 844ins68 polymorphism in Sickle cell disease patients: Frequency of vaso-occlusive crisis. |
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Priority needs and wisdom strategy for blood transfusion safety in developing low-resource countries. |
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Study of red blood cellalloimmunization risk factors in multiply transfused thalassemia patients:role in improving thalassemia transfusion practice in Fayoum, Egypt. |
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A preliminary Study of Clinically Significant Red Cell Antigen Phenotypes in Fayoum Blood Donors. |
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Early predictors of suboptimal response to CML therapy could help in determining the treatment strategy |
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Immunophenotyping of Circulating Mononuclear Cells in Active Pulmonary Tuberculosis |
Study of some ameliorating factors in ?-thalassemia, The Medical Journal of Cairo University (2007)
Prenatal diagnosis of beta-thalassemia in Egypt: Implementing accurate high- tech methods did not reflect much on the outcome. Pediatric Hematology and Oncology (2008); 25 (6): 541 - 548. DOI:10.1080/08880010802313509
Circulating micro-particles as potential hemostatic biomarkers for cerebrovascular ischemic infarction. The Journal of the Egyptian Society of Hematology and Research(2012); 8 (1): 21 - 26
Use of denaturing gradient gel electrophoresis in screening unknown ?-thalassemia mutations in Egyptian patients. Egyptian Journal of Medical Human Genetics (2012); 13 (3): 343 – 349. DOI:10.1016/j.ejmhg.2012.06.008
Prognostic value of cyclin E and cyclin dependent kinase inhibitor (P27) gene expression in non - Hodgkin's lymphoma. Life Science Journal (2012); 9 (2): 692 - 699
The use of soluble intercellular adhesion molecule-1 and soluble vascular cell adhesion molecule -1 as potential biomarkers in patients with atherosclerotic cerebrovascular disease. Medical Journalof Cairo University (2012)
Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt. Transfusion (2013); 53: 2940 - 2944.
DOI:10.1111/trf.12100
A disintegrin and metalloproteinase 33 (ADAM33) gene polymorphism association with asthma in Egyptian children. Egyptian Journal of Medical Human Genetics (2013); 14 (1): 55 - 62.
DOI.10.1016/j.ejmhg.2012.08.005
Multidrug and toxin extrusion protein (MATE1) gene polymorphism and therapeutic effects of metformin in type 2 diabetes. Journal of Applied Medical Sciences (2014); 3 (4): 73-84 ISSN: 2241 - 2328
Priority needs and wisdom strategy for blood transfusion safety in developing low resource countries. Transfus. Apheresis Sci. (2016); 54:147 -149.
DOI:10.1016/j.transci.2015.12.003
B-type natriuretic peptide as an index of symptoms and severity of rheumatic mitral regurgitation. Heart Views (2016); 17 (1): 7 - 12.
DOI:10.4103/1995-705X.182648
Study of red blood cell alloimmunization risk factors in multiply transfused thalassemia patients: role in improving thalassemia transfusion practice in Fayoum, Egypt. Transfusion (2016); 56: 2303 - 2307. DOI: 10.1111/trf.13695
Cystathionine Beta Synthase (CBS) gene844 ins68 polymorphism in sickle cell disease patients: Frequency of vaso-occusive crisis. The Journal of the Egyptian Society of Haematology and Research (2017); 13 (2): 43 - 48
A preliminary study of clinically significant red cell antigen phenotypes in fayoum blood donors. Journal of the Egyptian Society of Haematology and Research (2017); 13 (1): 13 - 17
Early predictors of suboptimal response CML therapy could help in determining treatment strategy. International Journal of Hematology and Oncology (2018); 28(3): 154 - 161
Immunophenotyping of circulating mononuclear cells in active pulmonary tuberculosis. The Journal of Infection in Developing Countries (2018); 12 (12):1073 - 1078. DOI: 10.3855/jidc.10171
Clinically significant red cell antigen phenotypes in Fayoum university hospital blood donors. Fayoum University Medical Journal (2020); 5 (1): 41- 45. DOI: 10.21608/fumj.2020.77470
Role of insulin-like growth factor 1 in pathogenesis of acne vulgaris: relation to acne severity and body mass index. International Journal of Research in Dermatology (2020); 6 (2): 147 - 150.
DOI:10.18203/issn.2455-4529.IntJResDermatol20200593
An SP1-binding site polymorphism in the COLIA1 gene and its relation to osteoporosis in Egyptian patients with Gaucher disease. The 6th Annual Summit on Rare Disease and Orphan and the 12th International Conference on Bacteriology and Infectious Diseases. Journal of Infectious Disease and Therapy (2022); Vol. 10:17
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