Fawzia Amer

7PUBLICATIONS
21CO-AUTHORS
Major global burdens of diseaseEpigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesMedical infection agents (incl. prions)Forensic epidemiology
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Publications (7)

|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

|Feb 16, 2024
STAC3-related myopathy: A Report of a Cohort of Seven Saudi Arabian Patients.

Momen Almomen, Fawzia Amer, Fatima Alfaraj

|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

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