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Oral health status of Egyptian children with lysosomal storage diseases: An evaluation of dental indices, salivary cytokines level, and bacterial bioburden

International journal of paediatric dentistry, 2024-05

2024

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Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Annals of Pediatric Endocrinology & Metabolism, 2022, 27(3), , pp.214-222

2022

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Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion

The Egyptian journal of medical human genetics, 2024-07, Vol.25 (1), p.88

2024

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Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome

American journal of human genetics, 2011-01, Vol.88 (1), p.92-98

2011

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Results From a 12-Month Open-Label Phase 1/2 Study of Velaglucerase Alfa in Children and Adolescents With Type 3 Gaucher Disease

Journal of inborn errors of metabolism and screening, 2018, Vol.6, p.232640981876556

2018

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An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

European journal of human genetics : EJHG, 2022-09, Vol.30 (9), p.1029-1035

2022

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Hyperimmunoglobulinemia and IgG Subclass Abnormalities in Children With Gaucher Disease

Journal of pediatric hematology/oncology, 2019-10, Vol.41 (7), p.e416

2019

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Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Annals of pediatric endocrinology & metabolism, 2022-09, p.214-222

2022

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Prevalence of celiac disease among children with Down syndrome attending the genetics clinic at Alexandria University Children Hospital

Alexandria Journal of Pediatrics, 2020-01, Vol.33 (1), p.1

2020

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Mutations in ALDH1A3 Represent a Frequent Cause of Microphthalmia/Anophthalmia in Consanguineous Families

Human mutation, 2014-08, Vol.35 (8), p.949-953

2014

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Velaglucerase alfa enzyme replacement therapy in children and adolescents with type 3 Gaucher disease: Results of a 12-month multicenter, open-label phase 1/2 study

Molecular genetics and metabolism, 2016-02, Vol.117 (2), p.S111-S111

2016

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Registry of ocular anomalies among patients with genetic disorders in Alexandria and nearby governorates

Alexandria Journal of Pediatrics, 2019-01, Vol.32 (1), p.55

2019

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Clinical characteristics of type III Gaucher disease in children and adolescents enrolled in a trial of velaglucerase alfa

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.S21-S21

2015

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RAX and anophthalmia in humans: evidence of brain anomalies

Molecular vision, 2012-06, Vol.18, p.1449-1456

2012

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COAGULATION ABNORMALITIES IN TYPE 1 GAUCHER DISEASE IN CHILDREN

Pediatric hematology and oncology, 2006-07, Vol.23 (5), p.411-417

2006

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Molecular basis of beta-thalassemia in Alexandria

The Egyptian journal of immunology, 2005, Vol.12 (1), p.15

2005

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Markers of apoptosis and proliferation related gene products as predictors of treatment outcome in childhood acute lymphoblastic leukemia

Hematology (Luxembourg), 2007-06, Vol.12 (3), p.209-218

2007

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Late-onset systemic lupus erythematosus: characteristics and outcome in comparison to juvenile- and adult-onset patients—a multicenter retrospective cohort

Clinical rheumatology, 2020-02, Vol.39 (2), p.435-442

2020

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Comparative Taxonomic Study of Launaea Cass. (Asteraceae, Cichorioideae) in Egypt

Taxonomy (Basel, Switzerland), 2021-09, Vol.1 (3), p.192-209

2021

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A comparative study between the disease characteristics in adult-onset and childhood-onset systemic lupus erythematosus in Egyptian patients attending a large university hospital

Lupus, 2021-02, Vol.30 (2), p.211-218

2021

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Ultrasound Hand and Wrist Findings in Children with Systemic Lupus Erythematosus

Current rheumatology reviews, 2023-01, Vol.19 (2), p.197

2023

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Effect of an increased dose of colchicine on microalbuminuria in children with Familial Mediterranean Fever

Egyptian rheumatologist, 2020-04, Vol.42 (2), p.141-145

2020

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Assessment of Lupus Nephritis in a Multicenter Retrospective Egyptian Cohort: Initial Characteristics, Influence of Age and Gender, Outcome, and Potential Association with Disease Damage

Saudi journal of kidney diseases and transplantation, 2022-01, Vol.33 (1), p.90-105

2022

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Serum Amyloid A Level in Egyptian Children with Familial Mediterranean Fever

International Journal of Rheumatology, 2016-01, Vol.2016, p.7354018-6

2016

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Challenges During Review of COVID-19 Research Proposals: Experience of Faculty of Medicine, Ain Shams University Research Ethics Committee, Egypt

Frontiers in medicine, 2021-11, Vol.8, p.715796-715796

2021

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Oral health status of Egyptian children with lysosomal storage diseases: An evaluation of dental indices, salivary cytokines level, and bacterial bioburden

Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion

Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome

Results From a 12-Month Open-Label Phase 1/2 Study of Velaglucerase Alfa in Children and Adolescents With Type 3 Gaucher Disease

An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

Hyperimmunoglobulinemia and IgG Subclass Abnormalities in Children With Gaucher Disease

Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Prevalence of celiac disease among children with Down syndrome attending the genetics clinic at Alexandria University Children Hospital

Mutations in ALDH1A3 Represent a Frequent Cause of Microphthalmia/Anophthalmia in Consanguineous Families

Velaglucerase alfa enzyme replacement therapy in children and adolescents with type 3 Gaucher disease: Results of a 12-month multicenter, open-label phase 1/2 study

Registry of ocular anomalies among patients with genetic disorders in Alexandria and nearby governorates

Clinical characteristics of type III Gaucher disease in children and adolescents enrolled in a trial of velaglucerase alfa

RAX and anophthalmia in humans: evidence of brain anomalies

COAGULATION ABNORMALITIES IN TYPE 1 GAUCHER DISEASE IN CHILDREN

Molecular basis of beta-thalassemia in Alexandria

Markers of apoptosis and proliferation related gene products as predictors of treatment outcome in childhood acute lymphoblastic leukemia

Late-onset systemic lupus erythematosus: characteristics and outcome in comparison to juvenile- and adult-onset patients—a multicenter retrospective cohort

Comparative Taxonomic Study of Launaea Cass. (Asteraceae, Cichorioideae) in Egypt

A comparative study between the disease characteristics in adult-onset and childhood-onset systemic lupus erythematosus in Egyptian patients attending a large university hospital

Ultrasound Hand and Wrist Findings in Children with Systemic Lupus Erythematosus

Effect of an increased dose of colchicine on microalbuminuria in children with Familial Mediterranean Fever

Assessment of Lupus Nephritis in a Multicenter Retrospective Egyptian Cohort: Initial Characteristics, Influence of Age and Gender, Outcome, and Potential Association with Disease Damage

Serum Amyloid A Level in Egyptian Children with Familial Mediterranean Fever

Challenges During Review of COVID-19 Research Proposals: Experience of Faculty of Medicine, Ain Shams University Research Ethics Committee, Egypt

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