Isra Z. M. Eltazi

Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview

G. Stevanin, L. Elsayed, A. Ahmed, 2021, Frontiers in Molecular Biosciences.

Hereditary spastic paraplegias: time for an objective case definition and a new nosology for neurogenetic disorders to facilitate biomarker/therapeutic studies

G. Stevanin, L. Elsayed, A. Ahmed, 2019, Expert review of neurotherapeutics.

Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy.

J. Altmüller, M. Toliat, M. Koko, 2024, European journal of human genetics : EJHG.

Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia

F. Lamari, A. Brice, G. Stevanin, 2021, Frontiers in Neurology.