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Circulating soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) as diagnostic and prognostic marker in neonatal sepsis

Cytokine (Philadelphia, Pa.), 2014-02, Vol.65 (2), p.184-191

2014

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Efficacy and safety of a novel combination of two oral chelators deferasirox/deferiprone over deferoxamine/deferiprone in severely iron overloaded young beta thalassemia major patients

European journal of haematology, 2015-11, Vol.95 (5), p.411-420

2015

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Regulatory T cells with CD62L or TNFR2 expression in young type 1 diabetic patients: relation to inflammation, glycemic control and micro-vascular complications

Journal of diabetes and its complications, 2015-01, Vol.29 (1), p.120-126

2015

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Inhibitory effect of silver nanoparticles mediated by atmospheric pressure air cold plasma jet against dermatophyte fungi

Journal of medical microbiology, 2015-10, Vol.64 (10), p.1151-1161

2015

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Deferiprone vs deferoxamine for transfusional iron overload in SCD and other anemias: a randomized, open-label noninferiority study

Blood advances, 2022-02, Vol.6 (4), p.1243-1254

2022

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Deferiprone for transfusional iron overload in sickle cell disease and other anemias: open-label study of up to 3 years

Blood advances, 2023-02, Vol.7 (4), p.611-619

2023

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Pulmonary manifestations in young Gaucher disease patients: Phenotype‐genotype correlation and radiological findings

Pediatric pulmonology, 2020-02, Vol.55 (2), p.441-448

2020

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Management of Children With β-Thalassemia Intermedia: Overview, Recent Advances, and Treatment Challenges

Journal of pediatric hematology/oncology, 2018-05, Vol.40 (4), p.253-268

2018

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Retinal changes in children and adolescents with sickle cell disease attending a paediatric hospital in Cairo, Egypt: risk factors and relation to ophthalmic and cerebral blood flow

Transactions of the Royal Society of Tropical Medicine and Hygiene, 2013-04, Vol.107 (4), p.205-211

2013

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Cultural preferences and limited public resources influence the spectrum of thalassemia in Egypt

Journal of pediatric hematology/oncology, 2015-05, Vol.37 (4), p.281-284

2015

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Flow cytometric assessment of circulating platelet and erythrocytes microparticles in young thalassemia major patients: relation to pulmonary hypertension and aortic wall stiffness

European journal of haematology, 2013-06, Vol.90 (6), p.508-518

2013

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Methylene tetrahydrofolate reductase gene polymorphism in Egyptian children with acute lymphoblastic leukemia

Blood coagulation & fibrinolysis, 2010-01, Vol.21 (1), p.28-34

2010

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P1462: NEUROCOGNITIVE FUNCTION AND PSYCHOLOGICAL ASSESSMENT IN TRANSFUSION‐DEPENDENT BETA‐THALASSEMIA PATIENTS: RELATION TO BRAIN IRON CONTENT

HemaSphere, 2023-08, Vol.7 (S3), p.e185302c-n/a

2023

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PB2493: PERIPHERAL NEUROPATHY A HIDDEN CAUSE FOR PAIN IN GAUCHER DISEASE.A CASE REPORT AND REVIEW OF LITERATURE

HemaSphere, 2023-08, Vol.7 (S3), p.e32318bb-n/a

2023

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Serum progranulin levels in paediatric patients with Gaucher disease; relation to disease severity and liver stiffness by transient elastography

Liver international, 2020-12, Vol.40 (12), p.3051-3060

2020

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Endothelial nitric oxide synthase gene intron 4 variable number tandem repeat polymorphism in β-thalassemia major: relation to cardiovascular complications

Blood coagulation & fibrinolysis, 2015-06, Vol.26 (4), p.419-425

2015

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Cognitive decline and depressive symptoms: early non-motor presentations of parkinsonism among Egyptian Gaucher patients

Neurogenetics, 2020-07, Vol.21 (3), p.159-167

2020

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Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients

European journal of haematology, 2013-12, Vol.91 (6), p.522-533

2013

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A longitudinal prospective study of bleeding diathesis in Egyptian pediatric patients: single-center experience

Blood coagulation & fibrinolysis, 2012-07, Vol.23 (5), p.411-418

2012

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Influence of thiopurine methyltransferase gene polymorphism on Egyptian children with acute lymphoblastic leukaemia

Journal of genetics, 2017-12, Vol.96 (6), p.905-910

2017

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Enhancement of the antidermatophytic activity of silver nanoparticles by Q-switched Nd:YAG laser and monoclonal antibody conjugation

Medical mycology (Oxford), 2017-07, Vol.55 (5), p.495-506

2017

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Surfactant protein D as a marker for pulmonary complications in pediatric patients with sickle cell disease: Relation to lung function tests

Pediatric pulmonology, 2019-05, Vol.54 (5), p.610-619

2019

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Endothelial monocyte activating polypeptide II in children and adolescents with type 1 diabetes mellitus: Relation to micro-vascular complications

Cytokine (Philadelphia, Pa.), 2015-12, Vol.76 (2), p.156-162

2015

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Soluble Fas/FasL ratio as a marker of vasculopathy in children and adolescents with sickle cell disease

Cytokine (Philadelphia, Pa.), 2016-03, Vol.79, p.52-58

2016

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Clinical Predictive Value of Cystatin C in Pediatric Sickle Cell Disease: A Marker of Disease Severity and Subclinical Cardiovascular Dysfunction

Clinical and applied thrombosis/hemostasis, 2017-11, Vol.23 (8), p.1010-1017

2017

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Circulating soluble triggering receptor expressed on myeloid cells-1 (sTREM-1) as diagnostic and prognostic marker in neonatal sepsis

Efficacy and safety of a novel combination of two oral chelators deferasirox/deferiprone over deferoxamine/deferiprone in severely iron overloaded young beta thalassemia major patients

Regulatory T cells with CD62L or TNFR2 expression in young type 1 diabetic patients: relation to inflammation, glycemic control and micro-vascular complications

Inhibitory effect of silver nanoparticles mediated by atmospheric pressure air cold plasma jet against dermatophyte fungi

Deferiprone vs deferoxamine for transfusional iron overload in SCD and other anemias: a randomized, open-label noninferiority study

Deferiprone for transfusional iron overload in sickle cell disease and other anemias: open-label study of up to 3 years

Pulmonary manifestations in young Gaucher disease patients: Phenotype‐genotype correlation and radiological findings

Management of Children With β-Thalassemia Intermedia: Overview, Recent Advances, and Treatment Challenges

Retinal changes in children and adolescents with sickle cell disease attending a paediatric hospital in Cairo, Egypt: risk factors and relation to ophthalmic and cerebral blood flow

Cultural preferences and limited public resources influence the spectrum of thalassemia in Egypt

Flow cytometric assessment of circulating platelet and erythrocytes microparticles in young thalassemia major patients: relation to pulmonary hypertension and aortic wall stiffness

Methylene tetrahydrofolate reductase gene polymorphism in Egyptian children with acute lymphoblastic leukemia

P1462: NEUROCOGNITIVE FUNCTION AND PSYCHOLOGICAL ASSESSMENT IN TRANSFUSION‐DEPENDENT BETA‐THALASSEMIA PATIENTS: RELATION TO BRAIN IRON CONTENT

PB2493: PERIPHERAL NEUROPATHY A HIDDEN CAUSE FOR PAIN IN GAUCHER DISEASE.A CASE REPORT AND REVIEW OF LITERATURE

Serum progranulin levels in paediatric patients with Gaucher disease; relation to disease severity and liver stiffness by transient elastography

Endothelial nitric oxide synthase gene intron 4 variable number tandem repeat polymorphism in β-thalassemia major: relation to cardiovascular complications

Cognitive decline and depressive symptoms: early non-motor presentations of parkinsonism among Egyptian Gaucher patients

Therapeutic superiority and safety of combined hydroxyurea with recombinant human erythropoietin over hydroxyurea in young β-thalassemia intermedia patients

A longitudinal prospective study of bleeding diathesis in Egyptian pediatric patients: single-center experience

Influence of thiopurine methyltransferase gene polymorphism on Egyptian children with acute lymphoblastic leukaemia

Enhancement of the antidermatophytic activity of silver nanoparticles by Q-switched Nd:YAG laser and monoclonal antibody conjugation

Surfactant protein D as a marker for pulmonary complications in pediatric patients with sickle cell disease: Relation to lung function tests

Endothelial monocyte activating polypeptide II in children and adolescents with type 1 diabetes mellitus: Relation to micro-vascular complications

Soluble Fas/FasL ratio as a marker of vasculopathy in children and adolescents with sickle cell disease

Clinical Predictive Value of Cystatin C in Pediatric Sickle Cell Disease: A Marker of Disease Severity and Subclinical Cardiovascular Dysfunction

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