Heba A. Hassan

33 El Bohouth Street
Cairo, C 12311, Egypt

Last Updated: 09/26/2026

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Found 14 publications

Further characterization of the BRSK2-associated neurodevelopmental disorder.

Further characterization of the BRSK2-associated neurodevelopmental disorder.

Journal: European journal of human genetics : EJHG

Published: January 13, 2026

Clinical Utility of Genetic Diagnosis in Drug-Resistant Epilepsy: Refining Classification and Guiding Therapy in an Egyptian Cohort.

Clinical Utility of Genetic Diagnosis in Drug-Resistant Epilepsy: Refining Classification and Guiding Therapy in an Egyptian Cohort.

Journal: Clinical genetics

Published: November 20, 2025

Novel Homozygous DLX5 and WNT10B Variants Expand the Genetic and Phenotypic Spectrum of Autosomal Recessive Split-Hand/Foot Malformations (SHFM1D and SHFM6).

Novel Homozygous DLX5 and WNT10B Variants Expand the Genetic and Phenotypic Spectrum of Autosomal Recessive Split-Hand/Foot Malformations (SHFM1D and SHFM6).

Journal: Birth defects research

Published: October 20, 2025

Characterizing 46,XY Differences of Sex Development: Novel Genetic Variants and Diagnostic Pitfalls in a Single-Center Cohort.

Characterizing 46,XY Differences of Sex Development: Novel Genetic Variants and Diagnostic Pitfalls in a Single-Center Cohort.

Journal: Biochemical genetics

Published: August 22, 2025

Clinical and Genetic Characterization of CAPN3-Related Limb-Girdle Muscular Dystrophies in an Egyptian Cohort.

Clinical and Genetic Characterization of CAPN3-Related Limb-Girdle Muscular Dystrophies in an Egyptian Cohort.

Journal: Pediatric neurology

Published: August 16, 2025

Clinical and molecular characterization of chondrodysplasias in a cohort of Egyptian patients.

Clinical and molecular characterization of chondrodysplasias in a cohort of Egyptian patients.

Journal: Scientific reports

Published: April 17, 2025

Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II.

Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II.

Journal: Hormones (Athens, Greece)

Published: June 13, 2023

Insights on attenuating autophagy cellular and molecular pathways versus methotrexate-induced toxicity via liposomal turmeric therapy.

Insights on attenuating autophagy cellular and molecular pathways versus methotrexate-induced toxicity via liposomal turmeric therapy.

Journal: Journal, genetic engineering & biotechnology

Published: February 03, 2022

First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous CANT1 Mutations.

First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous CANT1 Mutations.

Journal: Molecular syndromology

Published: March 09, 2021

Quaternary diagnostics scheme for mucolipidosis II and detection of novel mutation in GNPTAB gene.

Quaternary diagnostics scheme for mucolipidosis II and detection of novel mutation in GNPTAB gene.

Journal: Journal, genetic engineering & biotechnology

Published: February 23, 2021

Topical Wound Healing Activity of Myricetin Isolated from Tecomaria capensis v. aurea.

Topical Wound Healing Activity of Myricetin Isolated from Tecomaria capensis v. aurea.

Journal: Molecules (Basel, Switzerland)

Published: September 27, 2020

Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I.

Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I.

Journal: Hormones (Athens, Greece)

Published: February 06, 2020

Showing 1-12 of 14

Last Updated: 09/26/2026