Ghada M H Abdel-Salam

23PUBLICATIONS
49CO-AUTHORS
NeurogeneticsMedical infection agents (incl. prions)NeonatologyGene expression (incl. microarray and other genome-wide approaches)Infant and child health
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Publications (23)

|Jan 22, 2026
A novel homozygous splicing variant in FRA10AC1: further delineation of the phenotype.

Mohamed S Abdel-Hamid, Ghada M H Abdel-Salam

|Dec 23, 2025
Refining the phenotypic spectrum of PNKP-related microcephaly: a study of 27 new patients.

Ghada M H Abdel-Salam, Mohamed S Abdel-Hamid, Sherif F Abdel-Ghafar

|Apr 30, 2025
New Phenotypes Associated With Pathogenic RNASEH2B and SAMHD1 Variants.

Ghada M H Abdel-Salam, Maha Eid, Manar A El-Serafy

|Feb 18, 2025
Delineating the Clinical and Brain Imaging Characteristics of the Neonatal Form of CSTB -Related Neurodevelopmental Disorders.

Mohamed S Abdel-Hamid, Sherif F Abdel-Ghafar, Inas S M Sayed

|Feb 17, 2025
RNA methyltransferase SPOUT1/CENP-32 links mitotic spindle organization with the neurodevelopmental disorder SpADMiSS.

Avinash V Dharmadhikari, Maria Alba Abad, Sheraz Khan

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