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Effect of renal failure and hemodialysis on some procoagulant aspects of hemostasis. The Journal of the Egyptian Society of Haematology and Research (2006); Vol. (2), No. (1) |
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Factor FVII Arg 353 Gln polymorphism and its relevance to ischemic complications following coronary catheter interventions. The Journal of the Egyptian Society of Haematology and Research (2006); Vol (2), No. (1) |
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Epilepsy, hyperhomocysteinemia and mutant methylenetetrahydrofolate reductase gene. Egypt J. Neurol. Psychiat. Neurosurg. (2006);Vol. 43 (2): 495 - 505 |
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Platelet glycoprotein [GPIIIA] gene polymorphism and aspirin resistance in patients with cerebrovascular accidents. The Medical Journal of Cairo University (2007); Vol. (75), No. (2) (Suppl. II) |
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Study of β-thalassemia mutations using the polymerase chain reaction-amplification refractory mutation system and direct DNA sequencing techniques in a group of Egyptian thalassemia patients. Hemoglobin (2007); 31(1): 63 - 69.
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Thrombophilia in patients with cryptogenic stroke. The Egyptian Journal of Neurology, Psychiatry (2008); 45 (2): 549 - 560 |
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Role of interleukin 6 and alpha-globulins in differentiating alzheimer and vascular dementias. Neurodegenerative Diseases (2012); 9(2): 81 - 86.
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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 |
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Combining serology and molecular typing of weak D role in improving D typing strategy in Egypt. Transfusion) 2013); 53: 2940 – 2944.
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The expression of IL-7RA in Egyptian patients with multiple sclerosis . Comparative Clinical Pathology (2015); 24 (5): 1223 - 1230.
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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 |
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The relationship between anemia, serum hepcidin levels, and chronic hepatitis C in chronic hemodialysis patients. The Egyptian Journal of Internal Medicine ( 2017); 29 (3): 112 - 116 |
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Reform Strategies of Medical Education in Egypt. Fayoum University Medical Journal (2018); 1 (1): 24 - 27. DOI: 10.21608/fumj.2018.5495
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Relation between red blood cell distribution width and left ventricular function in acute coronary syndrome patients. Fayoum University Medical Journal (2018): 1 (2): 19 - 35. DOI: 10.21608/fumj.2018.31293 |
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Assessment of serum level of vitamin D in infants and children with Down syndrome. Middle East Journal of Medical Genetics (2018); 7 (2): 104 - 111. DOI: 10.4103/MXE.MXE_10_18
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A study of transfusion related adverse events in Fayoum University Hospitals, Egypt: Hemovigilence initiative: PB2446. HemaSphere (2019); 3 (S1):1083. DOI: 10.1097/01.HS9.0000568244.62280.16 |
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Interleukin-1 β-511 and interleukin-6 gene polymorphisms in Egyptian children with febrile seizures. Journal of American Science (2019); 15 (10): 92 - 97. DOI: 10.7537/marsjas151019.12
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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
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Potential use of antigen-based rapid test for SARS-CoV-2 in respiratory specimens in low-resource settings in Egypt for symptomatic patients and high-risk contacts. Laboratory Medicine (2021); 52(2):e46-e49.
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Implication of folate deficiency in CYP2U1 loss of function . J Exp Med. (2021); 218 (11):e20210846. DOI: 10.1084/jem.20210846
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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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