Laila Selim

6PUBLICATIONS
35CO-AUTHORS
Major global burdens of diseaseEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Infant and child healthNeurology and neuromuscular diseases
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Publications (6)

|Feb 13, 2026
Clinical and genetic spectrum of L-dopa responsive dystonia: insights from seven Egyptian cases.

Nihal Almenabawy, Fawzia Amer, Laila Selim

|Oct 14, 2024
Clinical and Genetic Spectrum of Patients With Mitochondrial Disease in a Pediatric Egyptian Cohort: Novel Variants and Phenotypic Expansion.

Hebatallah M Hassaan, Angela Pyle, Nihal Almenabawy

|Jan 15, 2024
The clinical and genetic landscape of developmental and epileptic encephalopathies in Egyptian children.

Nour Elkhateeb, Mahmoud Y Issa, Hasnaa M Elbendary

|Aug 19, 2023
Clinical, biochemical, and molecular characterization of mucopolysaccharidosis type III in 34 Egyptian patients.

Nihal Almenabawy, Manal Ramadan, Mona Kamel

|Jan 07, 2023
Organic acidurias in Egyptian children: The urge for high-risk screening.

Dina A Mehaney, Zeinab S Seliem, Laila A Selim

|Sep 09, 2020
A relatively common homozygous TRAPPC4 splicing variant is associated with an early-infantile neurodegenerative syndrome.

Shereen G Ghosh, Marcello Scala, Christian Beetz

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