Nagia Fahmy

Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness

Kristen M. Laricchia, D. MacArthur, M. Lek, 2020, Genetics in Medicine.

SERUM LEVEL OF RETINOL BINDING PROTEIN 4 IN RELATION TO AMYOTROPHIC LATERAL SCLEROSIS AMONG EGYPTIAN PATIENTS

Nagia A. Fahmy, Rasha M Mamdouh, Randa A. Reda, 2022, Ain Shams Medical Journal.

Role of interleukin-6 in ischemic stroke outcome

H. Aref, A. Elsadek, S. Khalil, 2020, The Egyptian Journal of Neurology, Psychiatry and Neurosurgery.

MLPA analysis for molecular diagnosis of spinal muscular atrophy and correlation of 5q13.2 genes with disease phenotype in Egyptian patients

M. Zaki, M. Issa, M. Essawi, 2022, Egyptian Journal of Medical Human Genetics.

Ambulatory Duchenne Muscular Dystrophy Children: Cross-sectional Correlation between Function, Quantitative Muscle Ultrasound and MRI

H. Elsedfy, T. El-Sobky, H. Sakr, 2021, medRxiv.

Serum Soluble Vascular Cell Adhesion Molecule-1 ( sVCAM-1 ) in Acute Ischemic Stroke

A. Nassef, Hala M. El-Khawas, Nagia A. Fahmy, 2008 .

Vitamin D receptor gene polymorphism in patients with osteomalacic myopathy in Egypt

H. Shokri, A. Ghareeb, Nagia A. Fahmy, 2020, Neurological Sciences.

Egyptian adaptation and validation of the Edinburgh Cognitive and Behavioral Amyotrophic Lateral Sclerosis Screen (ECAS-EG)

Hebatallah R. Rashed, R. Moustafa, N. Hamdi, 2023, Neurological Sciences.

MicroRNAs as a Tool for Differential Diagnosis of Neuromuscular Disorders

Ahmed Abdellatif, Nahla O. Mousa, Nagia Fahmy, 2023, Neuromolecular medicine.