Nesma M. Elaraby

Cairo, C, Egypt

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 23 publications

Evaluating SEPHS2 expression and glutathione peroxidase as biomarkers in recurrent pregnancy loss: a new insight.

Evaluating SEPHS2 expression and glutathione peroxidase as biomarkers in recurrent pregnancy loss: a new insight.

Journal: Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals

Published: April 16, 2026

Expression levels of miR-146a-5p, miR-155-5p and the pro-inflammatory cytokine IL-8 in pregnant women with anti-phospholipid syndrome.

Expression levels of miR-146a-5p, miR-155-5p and the pro-inflammatory cytokine IL-8 in pregnant women with anti-phospholipid syndrome.

Journal: Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals

Published: March 04, 2026

Expression levels of miR-146a-5p, miR-155-5p and the pro-inflammatory cytokine IL-8 in pregnant women with anti-phospholipid syndrome.

Expression levels of miR-146a-5p, miR-155-5p and the pro-inflammatory cytokine IL-8 in pregnant women with anti-phospholipid syndrome.

Journal: Lupus

Published: February 25, 2026

Modulatory potential of A novel benzofuran-derived compound against aluminium chloride-induced neurotoxicity and miRNA dysregulation: Biochemical and bio-analytical study.

Modulatory potential of A novel benzofuran-derived compound against aluminium chloride-induced neurotoxicity and miRNA dysregulation: Biochemical and bio-analytical study.

Journal: Toxicology reports

Published: August 26, 2025

Genomic and clinical predictors of cardiovascular disease in Familial dyslipidemia: risk stratification in Egyptian adolescents and young adults.

Genomic and clinical predictors of cardiovascular disease in Familial dyslipidemia: risk stratification in Egyptian adolescents and young adults.

Journal: Lipids in health and disease

Published: July 28, 2025

Genetic etiology of inherited kidney diseases in egyptian patients: next generation sequencing identifies six novel variants.

Genetic etiology of inherited kidney diseases in egyptian patients: next generation sequencing identifies six novel variants.

Journal: Molecular and cellular pediatrics

Published: May 17, 2025

Gene editing using gamma modified PNA: HBB gene as a model.

Gene editing using gamma modified PNA: HBB gene as a model.

Journal: Journal, genetic engineering & biotechnology

Published: March 10, 2025

Association between GRIK1 rs363598 and intergenic rs360932 variants and susceptibility to autism spectrum disorders in Egyptian children.

Association between GRIK1 rs363598 and intergenic rs360932 variants and susceptibility to autism spectrum disorders in Egyptian children.

Journal: BMC pediatrics

Published: February 07, 2025

Correction: Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study.

Correction: Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study.

Journal: Molecular biology reports

Published: September 21, 2024

Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study.

Association of MTR and MTRR polymorphisms with recurrent pregnancy loss: a case control study.

Journal: Molecular biology reports

Published: June 25, 2024

Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene.

Correction to: Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene.

Journal: Journal of molecular neuroscience : MN

Published: May 31, 2024

Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patients.

Clinical and molecular characterization of myotonia congenita using whole-exome sequencing in Egyptian patients.

Journal: Molecular biology reports

Published: March 28, 2024

Showing 1-12 of 23

Last Updated: 09/26/2026