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Prevalence and risk factors of cognitive impairment in children with sickle cell disease in Egypt

International journal of hematology, 2022-03, Vol.115 (3), p.399-405

2022

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Comparing different markers of tubular dysfunction in transfusion-dependent thalassemia patients

International urology and nephrology, 2022-02, Vol.54 (2), p.421-428

2022

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A guide for evaluation of online learning in medical education: a qualitative reflective analysis

BMC medical education, 2021-06, Vol.21 (1), p.339-339, Article 339

2021

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The Cause-Effect Dilemma of Hematologic Changes in COVID-19: One Year after the Start of the Pandemic

Hematology reports, 2022-03, Vol.14 (2), p.95-102

2022

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Intracranial hemorrhage in primary immune thrombocytopenia (ITP): 20 years’ experience in pediatrics

European journal of pediatrics, 2021-05, Vol.180 (5), p.1545-1552

2021

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Evaluation of pulmonary function in Egyptian children with sickle cell disease: a single center study

The Gazette of the Egyptian Paediatric Association, 2024-07, Vol.72 (1), p.47-7, Article 47

2024

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Impact of Genetic Polymorphism of methylenetetrahydrofolate reductase C677T on Development of Hyperhomocysteinemia and Related Oxidative Changes in Egyptian β-Thalassemia Major Patients

PloS one, 2016-05, Vol.11 (5), p.e0155070-e0155070

2016

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Sickle cell disease: combination new therapies vs. CRISPR-Cas9 potential and challenges — review article

Annals of hematology, 2023-10

2023

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Diagnosis, management and prevention of Pediatric Acute Hemolytic Anemia: Egyptian adapted evidence-based clinical practice guidelines

The Gazette of the Egyptian Paediatric Association, 2023-12, Vol.71 (1), p.74-9, Article 74

2023

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Evidence-based Egyptian clinical practice guidelines: for the prevention and management of iron deficiency and iron deficiency anemia in infants, children and adolescents

Bulletin of the National Research Centre, 2023-12, Vol.47 (1), p.162-10, Article 162

2023

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The association between growth differentiation factor-15, erythroferrone, and iron status in thalassemic patients

Pediatric research, 2024-03, Vol.95 (4), p.1095-1100

2024

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Mitochondrial 3-hydroxymethylglutaryl-CoA synthase-2 (HMGCS2) deficiency: a rare case with bicytopenia and coagulopathy

BMJ case reports, 2023-11, Vol.16 (11)

2023

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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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The 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

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

2022

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ZAP-70 mutation: a case with familial autoimmune haemolytic anaemia and immune deficiency

BMJ case reports, 2024-03, Vol.17 (3)

2024

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Influence of iron regulating genes mutations on iron status in Egyptian patients with sickle cell disease

Annals of clinical and laboratory science, 2014, Vol.44 (3), p.304-309

2014

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Intracranial Hemorrhage in Egyptian Children with Primary Immune Thrombocytopenia (ITP): Report of 24 Cases in 20 Years

Blood, 2019-11, Vol.134 (Supplement_1), p.1080-1080

2019

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Novel marker for the detection of sickle cell nephropathy: soluble FMS-like tyrosine kinase-1 (sFLT-1)

Pediatric nephrology (Berlin, West), 2015-12, Vol.30 (12), p.2163-2168

2015

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Bone health in pediatric transfusion‐dependent beta‐thalassemia: Circulating osteoprotegerin and RANKL system

Pediatric blood & cancer, 2022-01, Vol.69 (1), p.e29377-n/a

2022

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Prevention of Hemoglobinopathies in Egypt

Hemoglobin, 2009, Vol.33 (S1), p.S14-S20

2009

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Effect of L-carnitine on the physical fitness of thalassemic patients

Annals of hematology, 2007-01, Vol.86 (1), p.31-34

2007

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Introduction

Medical education, 2015-05, Vol.49 (5), p.511-512

2015

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Introduction

Medical education, 2015-05, Vol.49 (5), p.511

2015

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Introduction

Medical education, 2015-05, Vol.49 (5), p.511-512

2015

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Prevalence and risk factors of cognitive impairment in children with sickle cell disease in Egypt

Comparing different markers of tubular dysfunction in transfusion-dependent thalassemia patients

A guide for evaluation of online learning in medical education: a qualitative reflective analysis

The Cause-Effect Dilemma of Hematologic Changes in COVID-19: One Year after the Start of the Pandemic

Intracranial hemorrhage in primary immune thrombocytopenia (ITP): 20 years’ experience in pediatrics

Evaluation of pulmonary function in Egyptian children with sickle cell disease: a single center study

Impact of Genetic Polymorphism of methylenetetrahydrofolate reductase C677T on Development of Hyperhomocysteinemia and Related Oxidative Changes in Egyptian β-Thalassemia Major Patients

Sickle cell disease: combination new therapies vs. CRISPR-Cas9 potential and challenges — review article

Diagnosis, management and prevention of Pediatric Acute Hemolytic Anemia: Egyptian adapted evidence-based clinical practice guidelines

Evidence-based Egyptian clinical practice guidelines: for the prevention and management of iron deficiency and iron deficiency anemia in infants, children and adolescents

Egyptian Pediatric Guidelines for the Management of Children with Isolated Thrombocytopenia Using the Adapted ADAPTE Methodology-A Limited-Resource Country Perspective

The association between growth differentiation factor-15, erythroferrone, and iron status in thalassemic patients

Mitochondrial 3-hydroxymethylglutaryl-CoA synthase-2 (HMGCS2) deficiency: a rare case with bicytopenia and coagulopathy

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

The 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

ZAP-70 mutation: a case with familial autoimmune haemolytic anaemia and immune deficiency

Influence of iron regulating genes mutations on iron status in Egyptian patients with sickle cell disease

Intracranial Hemorrhage in Egyptian Children with Primary Immune Thrombocytopenia (ITP): Report of 24 Cases in 20 Years

Novel marker for the detection of sickle cell nephropathy: soluble FMS-like tyrosine kinase-1 (sFLT-1)

Bone health in pediatric transfusion‐dependent beta‐thalassemia: Circulating osteoprotegerin and RANKL system

Prevention of Hemoglobinopathies in Egypt

Effect of L-carnitine on the physical fitness of thalassemic patients

Introduction

Introduction

Introduction

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