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Ophthalmic Genetics|March 30, 2023
Whole-exome screening for primary congenital glaucoma in LebanonNadine J Makhoul, Zahi Wehbi, Dalia El Hadi, et al.
Ophthalmic Genetics|November 30, 2020
KIF21A pathogenic variants cause congenital fibrosis of extraocular muscles type 3Christiane Al-Haddad, Rose-Mary Boustany, Elza Rachid, et al.
Neuroscience Letters|July 19, 2002
Allopregnanolone attenuates N-methyl-D-aspartate-induced excitotoxicity and apoptosis in the human NT2 cell line in cultureEllen M Lockhart, David S Warner, Robert D Pearlstein, et al.
IBRO Neuroscience Reports|July 18, 2025
Downregulation of AKT-mediated p27Kip1 phosphorylation with shift to sphingomyelin synthesis in CLN3 diseaseFatima Bilal, Jihane Soueid, Sara Saab, et al.
Frontiers in Neurology|March 7, 2019
Developmental Comparison of Ceramide in Wild-Type and Cln3 Δ Mouse Brains and SeraSally El-Sitt, Jihane Soueid, Jamal Al Ali, et al.
Scientific Reports|January 9, 2016
RYR2, PTDSS1 and AREG genes are implicated in a Lebanese population-based study of copy number variation in autismJihane Soueid, Silva Kourtian, Nadine J Makhoul, et al.
Cells|May 13, 2025
Expanded Phenotype of the Cln6 Mouse ModelVictoria Chaoul, Sara Saab, Omar Shmoury, et al.
Frontiers in Neurology|August 29, 2019
Pre- and Post-therapy Assessment of Clinical Outcomes and White Matter Integrity in Autism Spectrum Disorder: Pilot StudyStephanie Saaybi, Natally AlArab, Salem Hannoun, et al.
Electrophoresis|November 20, 2012
CLN5 and CLN8 protein association with ceramide synthase: biochemical and proteomic approachesSaria El Haddad, Marwan Khoury, Mohammad Daoud, et al.
Electrophoresis|November 20, 2012
Neuroproteomics approach and neurosystems biology analysis: ROCK inhibitors as promising therapeutic targets in neurodegeneration and neurotraumaMohamad Raad, Tala El Tal, Rukhsana Gul, et al.
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