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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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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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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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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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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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Does Autophagy have a Role in the Pathogenesis of Pediatric Hepatic Steatosis?

Asian Pacific Journal of Cancer Prevention, 2024-05, Vol.25 (5), p.1753-1761

2024

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Synthesis, characterization, and anticancer activity of new binuclear complexes of 2,2′‐malonylbis(N‐phenylhydrazine‐1‐carbothioamide)

Applied organometallic chemistry, 2021-05, Vol.35 (5), p.n/a

2021

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Effect of Adding Veggies Powdered on Physico-Chemical and Sensory Properties of Cookies

Food Technology Research Journal, 2023-09, Vol.2 (1), p.50-63

2023

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Detection of Renal Insufficiency in a Cohort of Patients With Beta-thalassemia Major Using Cystatin-C

Journal of pediatric hematology/oncology, 2021-11, Vol.43 (8), p.e1082-e1087

2021

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Altered Expression of MicroRNAs in the Bone Marrow of Multiple Myeloma Patients and their Relationship to Cytogenetic Aberrations

Current pharmaceutical biotechnology, 2020-01, Vol.21 (13), p.1394-1401

2020

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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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Diagnostic significance of miR‐21, miR‐141, miR‐18a and miR‐221 as novel biomarkers in prostate cancer among Egyptian patients

Andrologia, 2019-11, Vol.51 (10), p.e13384-n/a

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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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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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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Production optimization of invertase by Lactobacillus brevis Mm-6 and its immobilization on alginate beads

Carbohydrate polymers, 2013-04, Vol.93 (2), p.740-746

2013

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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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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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Perioperative Multimodal Analgesia Overview: Review Article

The Egyptian journal of hospital medicine, 2022-10, Vol.89 (1), p.5356-5361

2022

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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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Prognostic value of B-cell maturation antigen, CD56 expression and neutrophil lymphocyte ratio in patients with multiple myeloma

Acta haematologica polonica, 2022-10

2022

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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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Analgesic Options in the Prevention Post?Craniotomy Pain (PCP)

NeuroQuantology, 2022-01, Vol.20 (10), p.7534

2022

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

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

Assessment of pubertal development in Egyptian girls

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

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

Does Autophagy have a Role in the Pathogenesis of Pediatric Hepatic Steatosis?

Synthesis, characterization, and anticancer activity of new binuclear complexes of 2,2′‐malonylbis(N‐phenylhydrazine‐1‐carbothioamide)

Effect of Adding Veggies Powdered on Physico-Chemical and Sensory Properties of Cookies

Detection of Renal Insufficiency in a Cohort of Patients With Beta-thalassemia Major Using Cystatin-C

Altered Expression of MicroRNAs in the Bone Marrow of Multiple Myeloma Patients and their Relationship to Cytogenetic Aberrations

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

Diagnostic significance of miR‐21, miR‐141, miR‐18a and miR‐221 as novel biomarkers in prostate cancer among Egyptian patients

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

Biochemical diagnosis of Sanfilippo disorder types A and B

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

Production optimization of invertase by Lactobacillus brevis Mm-6 and its immobilization on alginate beads

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

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

Perioperative Multimodal Analgesia Overview: Review Article

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

Prognostic value of B-cell maturation antigen, CD56 expression and neutrophil lymphocyte ratio in patients with multiple myeloma

Indicators of the metabolic syndrome in obese adolescents

Analgesic Options in the Prevention Post?Craniotomy Pain (PCP)

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

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