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Association between BCL11A, HSB1L-MYB, and XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients

Annals of hematology, 2020-10, Vol.99 (10), p.2279-2288

2020

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Vitamin D Level and Disease Activity in Children with Juvenile Idiopathic Arthritis

Pediatric Sciences Journal, 2022-01, Vol.2 (1), p.25-31

2022

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Impact of Superoxide Dismutase Genetic Polymorphism (SOD2 Val16Ala) and Superoxide Dismutase Level on Disease Severity in a Cohort of Egyptian Sickle Cell Disease Patients

Mediterranean journal of hematology and infectious diseases, 2022-05, Vol.14 (1), p.e2022037-e2022037

2022

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Circulating T regulatory cells in patients with psoriasis with and without atherosclerosis: A pilot comparative study before and after photochemotherapy

Photodermatology, photoimmunology & photomedicine, 2021-11, Vol.37 (6), p.545-548

2021

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Diagnostic values of CD64, C-reactive protein and procalcitonin in ventilator-associated pneumonia in adult trauma patients: a pilot study

Clinical chemistry and laboratory medicine, 2016-05, Vol.54 (5), p.889

2016

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Inducible nitric oxide synthase promoter polymorphism: a molecular susceptibility marker for vitiligo in Egyptians

International journal of dermatology, 2015-06, Vol.54 (6), p.675-679

2015

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The clinical relevance and prognostic significance of adenosine triphosphate ATP-binding cassette (ABCB5) and multidrug resistance (MDR1) genes expression in acute leukemia: an Egyptian study

Journal of cancer research and clinical oncology, 2014-08, Vol.140 (8), p.1323-1330

2014

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Protein Z and Endothelin‐1 genetic polymorphisms in pediatric Egyptian sickle cell disease patients

Journal of clinical laboratory analysis, 2018-02, Vol.32 (2), p.n/a

2018

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Association of Interleukin-2-330T/G and Interleukin-10-1082A/G Genetic Polymorphisms with B-Cell Non-Hodgkin Lymphoma in a Cohort of Egyptians

Turkish journal of haematology, 2018-05, Vol.35 (2), p.99-108

2018

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Level of Interleukin 37 (IL-37) in Children with Systemic Lupus Erythematosus and Its Correlation with Disease Activity

Majallah-ʼi bīmārīhā-yi kūdakān-i Īrān = Iranian journal of pediatrics, 2018-02, Vol.28 (1)

2018

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Excision repair cross-complementing group 2/Xeroderma pigmentousm complementation group D (ERCC2/XPD) genetic variations and susceptibility to diffuse large B cell lymphoma in Egypt

International journal of hematology, 2013-12, Vol.98 (6), p.681-686

2013

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The link between genetic polymorphism of glutathione-S-transferases, GSTM1, and GSTT1 and diffuse large B-cell lymphoma in Egypt

Journal of cancer research and clinical oncology, 2012-08, Vol.138 (8), p.1363-1368

2012

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Prevalence of Hepatitis C among Egyptian Children with Sickle Cell Disease and the Role of IL28b Gene Polymorphisms in Spontaneous Viral Clearance

Mediterranean journal of hematology and infectious diseases, 2016, Vol.8 (1), p.e2016007-e2016007

2016

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FcγRIIa and FcγRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt

Blood coagulation & fibrinolysis, 2012-01, Vol.23 (1), p.64-68

2012

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Clinical implication of nucleophosmin gene mutation and Flt-3 internal tandem duplication in a cohort of Egyptian AML patients

Comparative clinical pathology, 2013-05, Vol.22 (3), p.497-506

2013

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Tumor necrosis factor α promotor polymorphism and nonsegmental vitiligo: a molecular susceptibility marker in Egyptian women

Journal of the Egyptian women's dermatologic society, 2014-05, Vol.11 (2), p.109-112

2014

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Genetic variations in tumor necrosis factor related apoptosis-inducing ligand receptor-1 (TRAIL-R1) gene and the susceptibility to b-cell non-hodgkin lymphoma (B-NHL) in Egypt1

Cancer biomarkers : section A of Disease markers, 2022-01, Vol.32 (4), p.451-458

2022

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The osteogenic differentiation potentials of umbilical cord blood hematopoietic stem cells

Comparative clinical pathology, 2012-08, Vol.21 (4), p.441-447

2012

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Prevalence of factor V Leiden (G1619A) and prothrombin gene (G20210A) mutation in Egyptian children with sickle cell disease

Comparative clinical pathology, 2013-07, Vol.22 (4), p.697-702

2013

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In vitro transdifferentiation of umbilical cord stem cells into cardiac myocytes: Role of growth factors

Egyptian Journal of Critical Care Medicine, 2013-04, Vol.1 (2), p.43-50

2013

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IMPACT OF SUPEROXIDE DISMUTASE GENETIC POLYMORPHISM (SOD2 VAL16ALA) AND SUPEROXIDE DISMUTASE LEVEL ON DISEASE SEVERITY IN A COHORT OF EGYPTIAN SICKLE CELL DISEASE PATIENTS IN EGYPT: SOD and SCD in Egypt

Mediterranean journal of hematology and infectious diseases, 2022-04, Vol.14 (1), p.e2022037

2022

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Mannose-binding lectin (MBL2) gene polymorphism in sickle cell anemia: an Egyptian study

Comparative clinical pathology, 2013-05, Vol.22 (3), p.387-394

2013

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IBCL-282: Genetic Polymorphisms of Death Receptor 4 (TRAIL-R1) and the Susceptibility to B-Non-Hodgkin Lymphoma among Egyptians

Clinical lymphoma, myeloma and leukemia, 2020-09, Vol.20, p.S281-S281

2020

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Genetic variations in tumor ecrosis factor related apoptosis-inducing ligand receptor-1 (TRAIL-R1) gene and the susceptibility to b-cell non-hodgkin lymphoma (B-NHL) in Egypt

Cancer biomarkers : section A of Disease markers, 2021, Vol.32 (4), p.451

2021

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Association of C46T genetic polymorphism of coagulation factor XII with deep venous thrombosis: a cohort study on Egyptian patients

Comparative clinical pathology, 2013-03, Vol.22 (2), p.203-207

2013

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Association between BCL11A, HSB1L-MYB, and XmnI γG-158 (C/T) gene polymorphism and hemoglobin F level in Egyptian sickle cell disease patients

Vitamin D Level and Disease Activity in Children with Juvenile Idiopathic Arthritis

Impact of Superoxide Dismutase Genetic Polymorphism (SOD2 Val16Ala) and Superoxide Dismutase Level on Disease Severity in a Cohort of Egyptian Sickle Cell Disease Patients

Circulating T regulatory cells in patients with psoriasis with and without atherosclerosis: A pilot comparative study before and after photochemotherapy

Diagnostic values of CD64, C-reactive protein and procalcitonin in ventilator-associated pneumonia in adult trauma patients: a pilot study

Inducible nitric oxide synthase promoter polymorphism: a molecular susceptibility marker for vitiligo in Egyptians

The clinical relevance and prognostic significance of adenosine triphosphate ATP-binding cassette (ABCB5) and multidrug resistance (MDR1) genes expression in acute leukemia: an Egyptian study

Protein Z and Endothelin‐1 genetic polymorphisms in pediatric Egyptian sickle cell disease patients

Association of Interleukin-2-330T/G and Interleukin-10-1082A/G Genetic Polymorphisms with B-Cell Non-Hodgkin Lymphoma in a Cohort of Egyptians

Level of Interleukin 37 (IL-37) in Children with Systemic Lupus Erythematosus and Its Correlation with Disease Activity

Excision repair cross-complementing group 2/Xeroderma pigmentousm complementation group D (ERCC2/XPD) genetic variations and susceptibility to diffuse large B cell lymphoma in Egypt

The link between genetic polymorphism of glutathione-S-transferases, GSTM1, and GSTT1 and diffuse large B-cell lymphoma in Egypt

Prevalence of Hepatitis C among Egyptian Children with Sickle Cell Disease and the Role of IL28b Gene Polymorphisms in Spontaneous Viral Clearance

FcγRIIa and FcγRIIIa genetic polymorphisms in a group of pediatric immune thrombocytopenic purpura in Egypt

Clinical implication of nucleophosmin gene mutation and Flt-3 internal tandem duplication in a cohort of Egyptian AML patients

Tumor necrosis factor α promotor polymorphism and nonsegmental vitiligo: a molecular susceptibility marker in Egyptian women

Genetic variations in tumor necrosis factor related apoptosis-inducing ligand receptor-1 (TRAIL-R1) gene and the susceptibility to b-cell non-hodgkin lymphoma (B-NHL) in Egypt1

The osteogenic differentiation potentials of umbilical cord blood hematopoietic stem cells

Prevalence of factor V Leiden (G1619A) and prothrombin gene (G20210A) mutation in Egyptian children with sickle cell disease

In vitro transdifferentiation of umbilical cord stem cells into cardiac myocytes: Role of growth factors

IMPACT OF SUPEROXIDE DISMUTASE GENETIC POLYMORPHISM (SOD2 VAL16ALA) AND SUPEROXIDE DISMUTASE LEVEL ON DISEASE SEVERITY IN A COHORT OF EGYPTIAN SICKLE CELL DISEASE PATIENTS IN EGYPT: SOD and SCD in Egypt

Mannose-binding lectin (MBL2) gene polymorphism in sickle cell anemia: an Egyptian study

IBCL-282: Genetic Polymorphisms of Death Receptor 4 (TRAIL-R1) and the Susceptibility to B-Non-Hodgkin Lymphoma among Egyptians

Genetic variations in tumor ecrosis factor related apoptosis-inducing ligand receptor-1 (TRAIL-R1) gene and the susceptibility to b-cell non-hodgkin lymphoma (B-NHL) in Egypt

Association of C46T genetic polymorphism of coagulation factor XII with deep venous thrombosis: a cohort study on Egyptian patients

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