Nagia Fahmy

6PUBLICATIONS
22CO-AUTHORS
African languagesNeurology and neuromuscular diseasesEpidemiological methodsGene mappingDevelopmental genetics (incl. sex determination)
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Publications (6)

|Dec 22, 2025
Translation and validation of the Arabic version of the amyotrophic lateral sclerosis assessment questionnaire (ALSAQ40-AR).

Radwa Soliman, Mahmoud S Swelam, Nagia Fahmy

|Mar 13, 2025
Headache types and characteristics in patients with Amyotrophic Lateral Sclerosis.

Radwa Soliman, Nagia Fahmy, Mahmoud S Swelam

|Sep 30, 2024
Clinical and epidemiological characteristics of amyotrophic lateral sclerosis in an Egyptian cohort.

Radwa Soliman, Enass Onbool, Kareem Omran

|Feb 26, 2024
Diagnosing missed cases of spinal muscular atrophy in genome, exome, and panel sequencing datasets.

Ben Weisburd, Rakshya Sharma, Villem Pata

|Feb 08, 2023
Egyptian adaptation and validation of the Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen (ECAS-EG).

Radwa Soliman, Hebatallah R Rashed, Ramez R Moustafa

|Dec 06, 2022
A novel homozygous p.Ser69Pro SOD1 mutation causes severe young-onset ALS with decreased enzyme activity.

Nagia Fahmy, Kathrin Müller, Peter Munch Andersen

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