Lamia Ali Pacha

Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1

Hans H. Jung, C. Tilikete, M. Koenig, 2018, JAMA neurology.

Multicenter Transversal Two-Phase Study to Determine a National Prevalence of Epilepsy in Algeria

S. Nouioua, M. Tazir, Lamia Ali Pacha, 2012, Neuroepidemiology.

Heterozygous EIF2AK2 Variant Causes Adolescence‐Onset Generalized Dystonia Partially Responsive to DBS

K. Bhatia, R. Maroofian, H. Houlden, 2021, Movement disorders clinical practice.

A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities

A. Munnich, D. Lessel, C. Kubisch, 2023, American journal of medical genetics. Part A.