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Long interspersed nuclear element-1 (LINE1)-mediated deletion of EVC, EVC2, C4orf6, and STK32B in Ellis-van Creveld syndrome with borderline intelligence

Human mutation, 2008-07, Vol.29 (7), p.931-938

2008

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Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development

American journal of medical genetics. Part A, 2021-06, Vol.185 (6), p.1666-1677

2021

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Congenital leptin and leptin receptor deficiencies in nine new families: identification of six novel variants and review of literature

Molecular genetics and genomics : MGG, 2023-07, Vol.298 (4), p.919-929

2023

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Identification of NR5A1 Mutations and Possible Digenic Inheritance in 46,XY Gonadal Dysgenesis

Sexual development, 2016-01, Vol.10 (3), p.147-151

2016

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Clinical and Radiographic Evaluation of Immediate Loaded Dental Implants With Local Application of Melatonin: A Preliminary Randomized Controlled Clinical Trial

The Journal of oral implantology, 2016-04, Vol.42 (2), p.119-125

2016

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Association of serum paraoxonase enzyme activity and oxidative stress markers with dyslipidemia in obese adolescents

Indian journal of endocrinology and metabolism, 2014-05, Vol.18 (3), p.340-344

2014

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A novel mutation in the leptin gene (W121X) in an Egyptian family

Molecular genetics and metabolism reports, 2014-01, Vol.1 (C), p.474-476

2014

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Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to ADIPOQ gene variants and body fat phenotype

The Egyptian journal of medical human genetics, 2015-10, Vol.16 (4), p.367-374

2015

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Assessment of pubertal development in Egyptian girls

Journal of Pediatric Endocrinology and Metabolism, 2005-06, Vol.18 (6), p.577

2005

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Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene

The journal of clinical endocrinology and metabolism, 2015-09, Vol.100 (9), p.3227-3230

2015

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AB002. Human genetics at the National Research Centre in Egypt: history, achievements and challenges

Annals of translational medicine, 2017-09, Vol.5 (S2), p.AB002-AB002

2017

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Biochemical diagnosis of Sanfilippo disorder types A and B

Journal of Genetic Engineering and Biotechnology, 2023-12, Vol.21 (1), p.112, Article 112

2023

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Indicators of the metabolic syndrome in obese adolescents

Archives of medical science, 2015-03, Vol.11 (1), p.92-98

2015

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Capturing complexity while being pressed for time

Staging Spectators in Immersive Performances, 2019, p.171-177

1, 2019

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The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy

Molecular neurobiology, 2024-08, Vol.61 (8), p.4949-4961

2024

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Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex development

European journal of endocrinology, 2014-05, Vol.170 (5), p.759-767

2014

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Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct Syndrome

Sexual development, 2017-01, Vol.11 (1), p.29-33

2017

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Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene

Journal of Pediatric Endocrinology and Metabolism, 2014-09, Vol.27 (9-10), p.873

2014

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A Novel Mutation (c.2735_2736delTC) in the Androgen Receptor Gene in 46,XY Females with Complete Androgen Insensitivity Syndrome in an Egyptian Family

Hormone research in paediatrics, 2014-01, Vol.82 (6), p.411-414

2014

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Clinical research: Indicators of the metabolic syndrome in obese adolescents

Archives of medical science, 2015-01, Vol.11 (1), p.92

2015

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Early-loaded laser-sintered versus acid-etched one-piece dental implants for mandibular premolars replacement: a preliminary study

Implant dentistry, 2014-10, Vol.23 (5), p.565-569

2014

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LASER sintered one-piece early-loaded dental implants for mandibular premolars replacement

The Journal of oral implantology, 2015-02, Vol.41 (1), p.56-62

2015

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Obesity in relation to inflammatory biomarkers, adiponectin gene variability, and insulin resistance among middle-aged Egyptian women

Middle East Journal of Medical Genetics, 2015-07, Vol.4 (2), p.70-76

2015

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Long interspersed nuclear element-1 (LINE1)-mediated deletion ofEVC,EVC2,C4orf6, andSTK32B in Ellis–van Creveld syndrome with borderline intelligence

Human mutation, 2008-07, Vol.29 (7), p.931-938

2008

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A clinical and genetic study of childhood and adolescent obesity

Middle East Journal of Medical Genetics, 2012-01, Vol.1 (1), p.18-25

2012

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Long interspersed nuclear element-1 (LINE1)-mediated deletion of EVC, EVC2, C4orf6, and STK32B in Ellis-van Creveld syndrome with borderline intelligence

Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development

Congenital leptin and leptin receptor deficiencies in nine new families: identification of six novel variants and review of literature

Identification of NR5A1 Mutations and Possible Digenic Inheritance in 46,XY Gonadal Dysgenesis

Clinical and Radiographic Evaluation of Immediate Loaded Dental Implants With Local Application of Melatonin: A Preliminary Randomized Controlled Clinical Trial

Association of serum paraoxonase enzyme activity and oxidative stress markers with dyslipidemia in obese adolescents

A novel mutation in the leptin gene (W121X) in an Egyptian family

Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to ADIPOQ gene variants and body fat phenotype

Assessment of pubertal development in Egyptian girls

Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene

AB002. Human genetics at the National Research Centre in Egypt: history, achievements and challenges

Biochemical diagnosis of Sanfilippo disorder types A and B

Indicators of the metabolic syndrome in obese adolescents

Capturing complexity while being pressed for time

The Diagnostic Value of Whole-Exome Sequencing in a Spectrum of Rare Neurological Disorders Associated with Cerebellar Atrophy

Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex development

Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct Syndrome

Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene

A Novel Mutation (c.2735_2736delTC) in the Androgen Receptor Gene in 46,XY Females with Complete Androgen Insensitivity Syndrome in an Egyptian Family

Clinical research: Indicators of the metabolic syndrome in obese adolescents

Early-loaded laser-sintered versus acid-etched one-piece dental implants for mandibular premolars replacement: a preliminary study

LASER sintered one-piece early-loaded dental implants for mandibular premolars replacement

Obesity in relation to inflammatory biomarkers, adiponectin gene variability, and insulin resistance among middle-aged Egyptian women

Long interspersed nuclear element-1 (LINE1)-mediated deletion ofEVC,EVC2,C4orf6, andSTK32B in Ellis–van Creveld syndrome with borderline intelligence

A clinical and genetic study of childhood and adolescent obesity

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